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Escherichia coli: Biology, Genetics, and Applications

At a Glance

Title: Escherichia coli: Biology, Genetics, and Applications

Total Categories: 5

Category Stats

  • Fundamental Biology and Ecology of *Escherichia coli*: 16 flashcards, 18 questions
  • *E. coli* as a Model Organism and in Biotechnology: 11 flashcards, 9 questions
  • Pathogenesis and Clinical Significance of *E. coli*: 18 flashcards, 12 questions
  • *E. coli* Genetics, Evolution, and Diversity: 13 flashcards, 20 questions
  • Specific Strains and Their Applications: 5 flashcards, 4 questions

Total Stats

  • Total Flashcards: 63
  • True/False Questions: 30
  • Multiple Choice Questions: 33
  • Total Questions: 63

Instructions

Click the button to expand the instructions for how to use the Wiki2Web Teacher studio in order to print, edit, and export data about Escherichia coli: Biology, Genetics, and Applications

Welcome to Your Curriculum Command Center

This guide will turn you into a Wiki2web Studio power user. Let's unlock the features designed to give you back your weekends.

The Core Concept: What is a "Kit"?

Think of a Kit as your all-in-one digital lesson plan. It's a single, portable file that contains every piece of content for a topic: your subject categories, a central image, all your flashcards, and all your questions. The true power of the Studio is speed—once a kit is made (or you import one), you are just minutes away from printing an entire set of coursework.

Getting Started is Simple:

  • Create New Kit: Start with a clean slate. Perfect for a brand-new lesson idea.
  • Import & Edit Existing Kit: Load a .json kit file from your computer to continue your work or to modify a kit created by a colleague.
  • Restore Session: The Studio automatically saves your progress in your browser. If you get interrupted, you can restore your unsaved work with one click.

Step 1: Laying the Foundation (The Authoring Tools)

This is where you build the core knowledge of your Kit. Use the left-side navigation panel to switch between these powerful authoring modules.

⚙️ Kit Manager: Your Kit's Identity

This is the high-level control panel for your project.

  • Kit Name: Give your Kit a clear title. This will appear on all your printed materials.
  • Master Image: Upload a custom cover image for your Kit. This is essential for giving your content a professional visual identity, and it's used as the main graphic when you export your Kit as an interactive game.
  • Topics: Create the structure for your lesson. Add topics like "Chapter 1," "Vocabulary," or "Key Formulas." All flashcards and questions will be organized under these topics.

🃏 Flashcard Author: Building the Knowledge Blocks

Flashcards are the fundamental concepts of your Kit. Create them here to define terms, list facts, or pose simple questions.

  • Click "➕ Add New Flashcard" to open the editor.
  • Fill in the term/question and the definition/answer.
  • Assign the flashcard to one of your pre-defined topics.
  • To edit or remove a flashcard, simply use the ✏️ (Edit) or ❌ (Delete) icons next to any entry in the list.

✍️ Question Author: Assessing Understanding

Create a bank of questions to test knowledge. These questions are the engine for your worksheets and exams.

  • Click "➕ Add New Question".
  • Choose a Type: True/False for quick checks or Multiple Choice for more complex assessments.
  • To edit an existing question, click the ✏️ icon. You can change the question text, options, correct answer, and explanation at any time.
  • The Explanation field is a powerful tool: the text you enter here will automatically appear on the teacher's answer key and on the Smart Study Guide, providing instant feedback.

🔗 Intelligent Mapper: The Smart Connection

This is the secret sauce of the Studio. The Mapper transforms your content from a simple list into an interconnected web of knowledge, automating the creation of amazing study guides.

  • Step 1: Select a question from the list on the left.
  • Step 2: In the right panel, click on every flashcard that contains a concept required to answer that question. They will turn green, indicating a successful link.
  • The Payoff: When you generate a Smart Study Guide, these linked flashcards will automatically appear under each question as "Related Concepts."

Step 2: The Magic (The Generator Suite)

You've built your content. Now, with a few clicks, turn it into a full suite of professional, ready-to-use materials. What used to take hours of formatting and copying-and-pasting can now be done in seconds.

🎓 Smart Study Guide Maker

Instantly create the ultimate review document. It combines your questions, the correct answers, your detailed explanations, and all the "Related Concepts" you linked in the Mapper into one cohesive, printable guide.

📝 Worksheet & 📄 Exam Builder

Generate unique assessments every time. The questions and multiple-choice options are randomized automatically. Simply select your topics, choose how many questions you need, and generate:

  • A Student Version, clean and ready for quizzing.
  • A Teacher Version, complete with a detailed answer key and the explanations you wrote.

🖨️ Flashcard Printer

Forget wrestling with table layouts in a word processor. Select a topic, choose a cards-per-page layout, and instantly generate perfectly formatted, print-ready flashcard sheets.

Step 3: Saving and Collaborating

  • 💾 Export & Save Kit: This is your primary save function. It downloads the entire Kit (content, images, and all) to your computer as a single .json file. Use this to create permanent backups and share your work with others.
  • ➕ Import & Merge Kit: Combine your work. You can merge a colleague's Kit into your own or combine two of your lessons into a larger review Kit.

You're now ready to reclaim your time.

You're not just a teacher; you're a curriculum designer, and this is your Studio.

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Text content is available under the Creative Commons Attribution-ShareAlike 4.0 License (opens in new tab). Additional terms may apply.

Disclaimer: This website is for informational purposes only and does not constitute any kind of advice. The information is not a substitute for consulting official sources or records or seeking advice from qualified professionals.


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Study Guide: Escherichia coli: Biology, Genetics, and Applications

Study Guide: Escherichia coli: Biology, Genetics, and Applications

Fundamental Biology and Ecology of *Escherichia coli*

Escherichia coli (E. coli) is a gram-negative, facultative anaerobic bacterium, typically inhabiting the lower intestine of warm-blooded organisms.

Answer: True

This statement accurately describes the fundamental characteristics and common habitat of *Escherichia coli*.

Related Concepts:

  • What is *Escherichia coli*, and where is it commonly found?: *Escherichia coli*, often abbreviated as *E. coli*, is a gram-negative, facultative anaerobic, rod-shaped bacterium belonging to the genus *Escherichia*. It is commonly found in the lower intestine of warm-blooded organisms.
  • Describe the key morphological and biological characteristics of *E. coli*.: *E. coli* is a gram-negative, facultative anaerobe, nonsporulating coliform bacterium. It is typically rod-shaped, measuring about 2.0 micrometers long and 0.25 to 1.0 micrometer in diameter. Its cell wall has a thin peptidoglycan layer and an outer membrane, which contributes to its gram-negative staining and provides resistance to certain antibiotics like penicillin.
  • When does *E. coli* typically colonize a newborn's gastrointestinal tract, and what is its role there?: *E. coli* usually colonizes an infant's gastrointestinal tract within 40 hours of birth, acquired from the environment or caregivers. In the large intestine, it adheres to the mucus and functions as the primary facultative anaerobe, remaining a benign commensal unless it acquires virulence factors.

*E. coli*'s cell wall structure, characterized by a thin peptidoglycan layer and an outer membrane, contributes to its Gram-negative staining and resistance to certain antibiotics, such as penicillin.

Answer: True

The Gram-negative cell wall composition of *E. coli*, featuring a thin peptidoglycan layer and an outer membrane, is indeed responsible for its staining properties and provides a degree of antibiotic resistance.

Related Concepts:

  • How does the cell wall structure of *E. coli* affect its Gram staining and antibiotic susceptibility?: *E. coli*'s cell wall consists of a thin peptidoglycan layer and an outer membrane. This structure causes it to stain gram-negative, appearing pink after the counterstain (safranin) in the Gram staining process. The outer membrane also acts as a barrier, protecting the cell from certain antibiotics, such as penicillin.
  • Describe the key morphological and biological characteristics of *E. coli*.: *E. coli* is a gram-negative, facultative anaerobe, nonsporulating coliform bacterium. It is typically rod-shaped, measuring about 2.0 micrometers long and 0.25 to 1.0 micrometer in diameter. Its cell wall has a thin peptidoglycan layer and an outer membrane, which contributes to its gram-negative staining and provides resistance to certain antibiotics like penicillin.

Under anaerobic conditions, *E. coli* primarily utilizes mixed acid fermentation, producing byproducts such as lactate and carbon dioxide.

Answer: True

Mixed acid fermentation is a key metabolic pathway for *E. coli* when oxygen is absent, yielding various acidic byproducts.

Related Concepts:

  • What are the primary metabolic capabilities of *E. coli* under anaerobic conditions?: Under anaerobic conditions, *E. coli* utilizes mixed acid fermentation, producing byproducts such as lactate, succinate, ethanol, acetate, and carbon dioxide. This process requires low levels of hydrogen gas, often achieved when *E. coli* coexists with hydrogen-consuming organisms like methanogens or sulfate-reducing bacteria.

*E. coli* primarily relies on the Entner-Doudoroff (EDP) pathway for glucose metabolism, although the EMPP pathway is thermodynamically more favorable.

Answer: False

*E. coli* predominantly utilizes the Embden-Meyerhof-Parnas (EMPP) and Pentose Phosphate Pathways (OPPP) for glucose metabolism, with the EDP pathway being more active during growth on gluconate.

Related Concepts:

  • What are the three native glycolytic pathways found in *E. coli*, and which are primarily used?: *E. coli* possesses three native glycolytic pathways: the Embden-Meyerhof-Parnas (EMPP) pathway, the Entner-Doudoroff (EDP) pathway, and the Pentose Phosphate Pathway (OPPP). While the EDP is thermodynamically more favorable, *E. coli* primarily relies on the EMPP and OPPP for glucose metabolism. The EDP is mainly active during growth on gluconate.

Catabolite repression in *E. coli* causes the bacterium to repress genes for less preferred sugars when preferred sugars are available.

Answer: True

Catabolite repression ensures that *E. coli* prioritizes the metabolism of more energetically favorable sugars, repressing the genes for less preferred ones when they are present.

Related Concepts:

  • What is catabolite repression, and how does it influence *E. coli*'s sugar metabolism?: Catabolite repression is a process where bacteria preferentially consume sugars that yield the highest growth rate. *E. coli* employs this mechanism by repressing the genes needed to metabolize less preferred sugars, ensuring that its limited metabolic resources are used for maximum growth. A common example is its preference for glucose over lactose.

*E. coli* optimally grows at temperatures around 10°C (50°F).

Answer: False

The optimal growth temperature for *E. coli* in laboratory settings is approximately 37°C (99°F).

Related Concepts:

  • What are the optimal conditions for *E. coli* growth in a laboratory setting?: *E. coli* optimally grows at 37°C (99°F), although some laboratory strains can multiply at temperatures up to 49°C (120°F). It can grow in various defined laboratory media, provided they contain essential nutrients like glucose, ammonium phosphate, sodium chloride, magnesium sulfate, and dipotassium phosphate.

The doubling rate of *E. coli* is influenced by nutrient availability and can be as fast as every 20 minutes under favorable conditions.

Answer: True

Under optimal nutrient conditions, *E. coli*'s rapid cell cycle allows for a doubling time as short as 20 minutes.

Related Concepts:

  • How is the bacterial cell cycle of *E. coli* divided, and what factors influence its doubling rate?: The bacterial cell cycle is divided into three periods: the B period (between cell division and DNA replication), the C period (DNA replication time), and the D period (between the end of DNA replication and cell division). The doubling rate of *E. coli* is influenced by nutrient availability; under favorable conditions, it can reproduce as quickly as every 20 minutes.
  • What are the optimal conditions for *E. coli* growth in a laboratory setting?: *E. coli* optimally grows at 37°C (99°F), although some laboratory strains can multiply at temperatures up to 49°C (120°F). It can grow in various defined laboratory media, provided they contain essential nutrients like glucose, ammonium phosphate, sodium chloride, magnesium sulfate, and dipotassium phosphate.

Synchronous replication in *E. coli* involves the simultaneous initiation of replication from all origins, leading to a 2n pattern of replication forks.

Answer: True

Synchronous replication in *E. coli* is characterized by the coordinated initiation of DNA replication from multiple origins, resulting in a 2n (or higher) number of replication forks.

Related Concepts:

  • What is meant by "synchronous replication" in *E. coli*?: Synchronous replication in *E. coli* occurs when replication is initiated simultaneously from all origins of replication, resulting in multiple replication forks along the DNA. This typically leads to the number of replication forks following a 2n pattern (where n is an integer), indicating that multiple rounds of replication are occurring concurrently within a single cell cycle.

Cellular aging in *E. coli* is characterized by the accumulation of damage in the "old pole" cell, which can lead to division arrest under stress.

Answer: True

The "old pole" of an *E. coli* cell can accumulate damage over successive divisions, potentially leading to division arrest and demonstrating a form of cellular aging.

Related Concepts:

  • How does cellular aging manifest in *E. coli*?: Although *E. coli* reproduces via binary fission, the resulting cells can be functionally asymmetric. The "old pole" cell may act as an aging parent, accumulating damage over time. When this damage exceeds an "immortality threshold" under elevated stress, the old pole cell can arrest division and become mortal, demonstrating a form of cellular aging that affects both prokaryotes and eukaryotes.

Histidine phosphorylation is a rare post-translational modification in *E. coli* proteins compared to serine phosphorylation.

Answer: False

Histidine phosphorylation is a notable post-translational modification observed in *E. coli* proteins, alongside serine, threonine, and tyrosine phosphorylation.

Related Concepts:

  • What types of post-translational modifications (PTMs) are observed in *E. coli* proteins?: While fewer bacterial proteins undergo PTMs compared to eukaryotes, *E. coli* proteins do exhibit modifications. Studies have identified numerous phosphoproteins, with phosphorylation occurring on serine, histidine, threonine, and tyrosine amino acid residues. Histidine phosphorylation is particularly notable in *E. coli*.

*E. coli* usually colonizes a newborn's gastrointestinal tract within 40 hours of birth, functioning as a benign commensal.

Answer: True

Early colonization of the infant gut by *E. coli* is typical, and most strains function as commensals, contributing to the normal microbiota.

Related Concepts:

  • When does *E. coli* typically colonize a newborn's gastrointestinal tract, and what is its role there?: *E. coli* usually colonizes an infant's gastrointestinal tract within 40 hours of birth, acquired from the environment or caregivers. In the large intestine, it adheres to the mucus and functions as the primary facultative anaerobe, remaining a benign commensal unless it acquires virulence factors.
  • What is the typical role of most *E. coli* strains in the human gut?: Most *E. coli* strains are part of the normal microbiota of the gut, where they are generally harmless or even beneficial. They can help produce vitamin K2 and prevent the colonization of the intestine by harmful pathogenic bacteria, representing a mutualistic relationship with humans.
  • What types of diseases can virulent *E. coli* strains cause?: Virulent *E. coli* strains can cause a range of diseases, including gastroenteritis, urinary tract infections (UTIs), neonatal meningitis, hemorrhagic colitis, and can be associated with Crohn's disease. In more severe cases, they can lead to complications like hemolytic-uremic syndrome (HUS), peritonitis, mastitis, sepsis, and pneumonia.

What is the primary role of most *E. coli* strains in the human gut?

Answer: Producing vitamin K2 and preventing colonization by harmful bacteria.

Most *E. coli* strains are commensal and contribute to host health by synthesizing vitamin K2 and inhibiting the growth of pathogenic bacteria.

Related Concepts:

  • What is the typical role of most *E. coli* strains in the human gut?: Most *E. coli* strains are part of the normal microbiota of the gut, where they are generally harmless or even beneficial. They can help produce vitamin K2 and prevent the colonization of the intestine by harmful pathogenic bacteria, representing a mutualistic relationship with humans.
  • What are some of the beneficial roles *E. coli* plays for its hosts?: Some strains of *E. coli* benefit their hosts by producing vitamin K2, which is essential for blood clotting and bone health. They also contribute to the host's health by preventing the growth of harmful bacteria in the intestine.
  • When does *E. coli* typically colonize a newborn's gastrointestinal tract, and what is its role there?: *E. coli* usually colonizes an infant's gastrointestinal tract within 40 hours of birth, acquired from the environment or caregivers. In the large intestine, it adheres to the mucus and functions as the primary facultative anaerobe, remaining a benign commensal unless it acquires virulence factors.

Which of the following is a key characteristic of *E. coli*'s cell wall that contributes to its Gram-negative staining?

Answer: A thin peptidoglycan layer and the presence of an outer membrane.

The Gram-negative staining of *E. coli* is a direct result of its cell wall structure, which includes a thin peptidoglycan layer and an outer membrane.

Related Concepts:

  • How does the cell wall structure of *E. coli* affect its Gram staining and antibiotic susceptibility?: *E. coli*'s cell wall consists of a thin peptidoglycan layer and an outer membrane. This structure causes it to stain gram-negative, appearing pink after the counterstain (safranin) in the Gram staining process. The outer membrane also acts as a barrier, protecting the cell from certain antibiotics, such as penicillin.
  • Describe the key morphological and biological characteristics of *E. coli*.: *E. coli* is a gram-negative, facultative anaerobe, nonsporulating coliform bacterium. It is typically rod-shaped, measuring about 2.0 micrometers long and 0.25 to 1.0 micrometer in diameter. Its cell wall has a thin peptidoglycan layer and an outer membrane, which contributes to its gram-negative staining and provides resistance to certain antibiotics like penicillin.

Under anaerobic conditions, *E. coli* primarily utilizes which metabolic process?

Answer: Mixed acid fermentation

In the absence of oxygen, *E. coli* relies on mixed acid fermentation to generate energy.

Related Concepts:

  • What are the primary metabolic capabilities of *E. coli* under anaerobic conditions?: Under anaerobic conditions, *E. coli* utilizes mixed acid fermentation, producing byproducts such as lactate, succinate, ethanol, acetate, and carbon dioxide. This process requires low levels of hydrogen gas, often achieved when *E. coli* coexists with hydrogen-consuming organisms like methanogens or sulfate-reducing bacteria.
  • What are the three native glycolytic pathways found in *E. coli*, and which are primarily used?: *E. coli* possesses three native glycolytic pathways: the Embden-Meyerhof-Parnas (EMPP) pathway, the Entner-Doudoroff (EDP) pathway, and the Pentose Phosphate Pathway (OPPP). While the EDP is thermodynamically more favorable, *E. coli* primarily relies on the EMPP and OPPP for glucose metabolism. The EDP is mainly active during growth on gluconate.

What is catabolite repression in *E. coli*?

Answer: A process where *E. coli* represses genes for less preferred sugars when preferred sugars are available.

Catabolite repression is a regulatory mechanism that prioritizes the metabolism of preferred carbon sources, suppressing the expression of genes for less preferred ones.

Related Concepts:

  • What is catabolite repression, and how does it influence *E. coli*'s sugar metabolism?: Catabolite repression is a process where bacteria preferentially consume sugars that yield the highest growth rate. *E. coli* employs this mechanism by repressing the genes needed to metabolize less preferred sugars, ensuring that its limited metabolic resources are used for maximum growth. A common example is its preference for glucose over lactose.

What is the optimal growth temperature for *E. coli* in a laboratory setting?

Answer: 37°C (99°F)

The optimal temperature for the growth of *E. coli* in laboratory conditions is 37°C.

Related Concepts:

  • What are the optimal conditions for *E. coli* growth in a laboratory setting?: *E. coli* optimally grows at 37°C (99°F), although some laboratory strains can multiply at temperatures up to 49°C (120°F). It can grow in various defined laboratory media, provided they contain essential nutrients like glucose, ammonium phosphate, sodium chloride, magnesium sulfate, and dipotassium phosphate.

What was the initial name given to *E. coli* by its discoverer, Theodor Escherich?

Answer: Bacterium coli commune

Theodor Escherich initially named the bacterium *Bacterium coli commune* upon its discovery in 1885.

Related Concepts:

  • Who discovered *E. coli*, and what was its initial name?: *E. coli* was discovered in 1885 by German-Austrian pediatrician Theodor Escherich. He initially named it *Bacterium coli commune* because he found it in the feces of healthy individuals, specifically in the colon.
  • What is *Escherichia coli*, and where is it commonly found?: *Escherichia coli*, often abbreviated as *E. coli*, is a gram-negative, facultative anaerobic, rod-shaped bacterium belonging to the genus *Escherichia*. It is commonly found in the lower intestine of warm-blooded organisms.
  • How did the classification of *E. coli* evolve over time?: Initially named *Bacterium coli commune*, it was later reclassified as *Bacillus coli* by Migula in 1895. Subsequently, it was placed in the newly created genus *Escherichia*, named after its discoverer, by Aldo Castellani and Albert John Chalmers.

What type of organism is *E. coli* classified as?

Answer: A bacterium

*Escherichia coli* is classified as a bacterium.

Related Concepts:

  • What is *Escherichia coli*, and where is it commonly found?: *Escherichia coli*, often abbreviated as *E. coli*, is a gram-negative, facultative anaerobic, rod-shaped bacterium belonging to the genus *Escherichia*. It is commonly found in the lower intestine of warm-blooded organisms.
  • Describe the key morphological and biological characteristics of *E. coli*.: *E. coli* is a gram-negative, facultative anaerobe, nonsporulating coliform bacterium. It is typically rod-shaped, measuring about 2.0 micrometers long and 0.25 to 1.0 micrometer in diameter. Its cell wall has a thin peptidoglycan layer and an outer membrane, which contributes to its gram-negative staining and provides resistance to certain antibiotics like penicillin.
  • How are *E. coli* strains classified phylogenetically, and what are the implications for pathology?: *E. coli* strains can be classified according to their phylogeny, or inferred evolutionary history, with species divided into groups. While whole genome sequencing yields robust phylogenies, the link between phylogenetic distance and pathology is often small. For example, strains within the O157:H7 clade (Group E) are all enterohaemorrhagic (EHEC), but not all EHEC strains are closely related.

*E. coli* as a Model Organism and in Biotechnology

*E. coli* is a crucial model organism in biotechnology and microbiology due to its ease of cultivation and well-characterized genetic structure, not its complexity or difficulty in cultivation.

Answer: True

The statement is corrected to reflect that *E. coli*'s utility as a model organism stems from its simplicity and ease of laboratory manipulation, not complexity or difficulty.

Related Concepts:

  • Why is *E. coli* considered a significant model organism in scientific research?: *E. coli* is the most widely studied prokaryotic model organism and is crucial in biotechnology and microbiology. It is easily grown and cultured in laboratories, has been intensively investigated for decades, and has served as the host organism for much of the work involving recombinant DNA technology.
  • How has *E. coli*'s adaptability and genetic tractability made it a valuable tool in biotechnology and biological engineering?: *E. coli*'s long history of laboratory use, ease of culture, and genetic manipulation have made it a cornerstone of biotechnology and industrial microbiology. Its role in creating recombinant DNA, pioneered by Cohen and Boyer, laid the foundation for producing heterologous proteins, including human insulin, and for various applications like vaccine development and bioremediation.
  • How has *E. coli* contributed to our understanding of fundamental biological processes?: *E. coli* has been instrumental in understanding key biological processes. It was used to first describe bacterial conjugation by Lederberg and Tatum, and its study with bacteriophages by researchers like Seymour Benzer helped elucidate the topography of gene structure. Its genome was also among the first to be sequenced, providing a foundational resource for molecular biology.

*E. coli*'s metabolism can be engineered to function as an autotroph by introducing carbon fixation genes and utilizing formate.

Answer: True

Through genetic engineering and laboratory evolution, *E. coli* can be adapted to fix carbon dioxide, thereby exhibiting autotrophic capabilities.

Related Concepts:

  • Can *E. coli*'s metabolism be altered to function as an autotroph, and if so, how?: Yes, *E. coli*'s metabolism can be rewired to use carbon dioxide (CO2) as its sole carbon source for biomass production, effectively displaying autotrophic capabilities. This is achieved by introducing carbon fixation genes and formate dehydrogenase, along with laboratory evolution experiments, allowing it to utilize formate to reduce electron carriers and generate ATP for anabolic pathways.

Studies investigating the *E. coli* interactome have shown limited overlap between different research studies, despite identifying thousands of interactions.

Answer: True

Research into the *E. coli* protein-protein interaction network (interactome) has revealed numerous interactions, but data consistency across studies remains a challenge, leading to limited overlap.

Related Concepts:

  • How has the interactome of *E. coli* been studied, and what are the findings regarding protein interactions?: The *E. coli* interactome has been investigated using methods like affinity purification coupled with mass spectrometry (AP/MS) and by analyzing binary protein-protein interactions. Studies have identified thousands of interactions, revealing complex networks and protein complexes, although data from different studies show limited overlap. A 2014 study mapped 2,234 protein-protein interactions using yeast two-hybrid screens.

E. coli is favored for producing recombinant proteins because it naturally exports many proteins into the periplasm, simplifying recovery.

Answer: False

While *E. coli* can be engineered for protein export, it does not naturally export a large quantity of proteins into the periplasm. The simplification of protein recovery and reduction of cross-contamination are achieved through other means, such as cell lysis, rather than extensive natural periplasmic export. Its popularity stems more from low cost, rapid growth, and ease of genetic modification.

Related Concepts:

  • Why is *E. coli* a preferred organism for producing therapeutic recombinant proteins?: While *E. coli* can be engineered for protein export, it does not naturally export a large quantity of proteins into the periplasm. The simplification of protein recovery and reduction of cross-contamination are achieved through other means, such as cell lysis, rather than extensive natural periplasmic export. Its popularity stems more from low cost, rapid growth, and ease of genetic modification.
  • How has *E. coli*'s adaptability and genetic tractability made it a valuable tool in biotechnology and biological engineering?: *E. coli*'s long history of laboratory use, ease of culture, and genetic manipulation have made it a cornerstone of biotechnology and industrial microbiology. Its role in creating recombinant DNA, pioneered by Cohen and Boyer, laid the foundation for producing heterologous proteins, including human insulin, and for various applications like vaccine development and bioremediation.
  • Beyond genetic experiments, what are some practical uses of *E. coli*?: *E. coli* has practical applications such as generating synthetic propane and producing recombinant human growth hormone. It also serves as a vector for various genetic engineering processes.

Why is *E. coli* considered an important model organism in scientific research?

Answer: It has been intensively investigated and is easily grown and cultured.

*E. coli*'s extensive study history, coupled with its ease of cultivation and genetic manipulation, makes it a cornerstone model organism in microbiology and biotechnology.

Related Concepts:

  • Why is *E. coli* considered a significant model organism in scientific research?: *E. coli* is the most widely studied prokaryotic model organism and is crucial in biotechnology and microbiology. It is easily grown and cultured in laboratories, has been intensively investigated for decades, and has served as the host organism for much of the work involving recombinant DNA technology.
  • How has *E. coli*'s adaptability and genetic tractability made it a valuable tool in biotechnology and biological engineering?: *E. coli*'s long history of laboratory use, ease of culture, and genetic manipulation have made it a cornerstone of biotechnology and industrial microbiology. Its role in creating recombinant DNA, pioneered by Cohen and Boyer, laid the foundation for producing heterologous proteins, including human insulin, and for various applications like vaccine development and bioremediation.
  • How has *E. coli* contributed to our understanding of fundamental biological processes?: *E. coli* has been instrumental in understanding key biological processes. It was used to first describe bacterial conjugation by Lederberg and Tatum, and its study with bacteriophages by researchers like Seymour Benzer helped elucidate the topography of gene structure. Its genome was also among the first to be sequenced, providing a foundational resource for molecular biology.

Which of the following is a key advantage of using *E. coli* for producing recombinant proteins?

Answer: It has a low cost, rapid growth, and ease of genetic modification.

*E. coli*'s cost-effectiveness, rapid proliferation, and amenability to genetic manipulation make it highly advantageous for recombinant protein production.

Related Concepts:

  • Why is *E. coli* a preferred organism for producing therapeutic recombinant proteins?: While *E. coli* can be engineered for protein export, it does not naturally export a large quantity of proteins into the periplasm. The simplification of protein recovery and reduction of cross-contamination are achieved through other means, such as cell lysis, rather than extensive natural periplasmic export. Its popularity stems more from low cost, rapid growth, and ease of genetic modification.
  • How has *E. coli*'s adaptability and genetic tractability made it a valuable tool in biotechnology and biological engineering?: *E. coli*'s long history of laboratory use, ease of culture, and genetic manipulation have made it a cornerstone of biotechnology and industrial microbiology. Its role in creating recombinant DNA, pioneered by Cohen and Boyer, laid the foundation for producing heterologous proteins, including human insulin, and for various applications like vaccine development and bioremediation.
  • Beyond genetic experiments, what are some practical uses of *E. coli*?: *E. coli* has practical applications such as generating synthetic propane and producing recombinant human growth hormone. It also serves as a vector for various genetic engineering processes.

*E. coli*'s role in creating recombinant DNA, pioneered by Cohen and Boyer, was foundational for producing which of the following?

Answer: Human insulin

The groundbreaking work using *E. coli* for recombinant DNA technology paved the way for the production of therapeutic proteins, notably human insulin.

Related Concepts:

  • How has *E. coli*'s adaptability and genetic tractability made it a valuable tool in biotechnology and biological engineering?: *E. coli*'s long history of laboratory use, ease of culture, and genetic manipulation have made it a cornerstone of biotechnology and industrial microbiology. Its role in creating recombinant DNA, pioneered by Cohen and Boyer, laid the foundation for producing heterologous proteins, including human insulin, and for various applications like vaccine development and bioremediation.

Which of the following is a practical use of *E. coli* mentioned in the source?

Answer: Generating synthetic propane

*E. coli* has been engineered for various biotechnological applications, including the synthesis of compounds like synthetic propane.

Related Concepts:

  • Beyond genetic experiments, what are some practical uses of *E. coli*?: *E. coli* has practical applications such as generating synthetic propane and producing recombinant human growth hormone. It also serves as a vector for various genetic engineering processes.
  • How has *E. coli*'s adaptability and genetic tractability made it a valuable tool in biotechnology and biological engineering?: *E. coli*'s long history of laboratory use, ease of culture, and genetic manipulation have made it a cornerstone of biotechnology and industrial microbiology. Its role in creating recombinant DNA, pioneered by Cohen and Boyer, laid the foundation for producing heterologous proteins, including human insulin, and for various applications like vaccine development and bioremediation.

What is the significance of *E. coli*'s genetic tractability in biotechnology?

Answer: It allows for easy genetic modification, enabling applications like vaccine development.

The genetic tractability of *E. coli* is fundamental to its widespread use in biotechnology, facilitating applications such as the development of vaccines and the production of therapeutic proteins.

Related Concepts:

  • How has *E. coli*'s adaptability and genetic tractability made it a valuable tool in biotechnology and biological engineering?: *E. coli*'s long history of laboratory use, ease of culture, and genetic manipulation have made it a cornerstone of biotechnology and industrial microbiology. Its role in creating recombinant DNA, pioneered by Cohen and Boyer, laid the foundation for producing heterologous proteins, including human insulin, and for various applications like vaccine development and bioremediation.
  • Why is *E. coli* considered a significant model organism in scientific research?: *E. coli* is the most widely studied prokaryotic model organism and is crucial in biotechnology and microbiology. It is easily grown and cultured in laboratories, has been intensively investigated for decades, and has served as the host organism for much of the work involving recombinant DNA technology.
  • How has *E. coli* contributed to our understanding of fundamental biological processes?: *E. coli* has been instrumental in understanding key biological processes. It was used to first describe bacterial conjugation by Lederberg and Tatum, and its study with bacteriophages by researchers like Seymour Benzer helped elucidate the topography of gene structure. Its genome was also among the first to be sequenced, providing a foundational resource for molecular biology.

Pathogenesis and Clinical Significance of *E. coli*

The majority of *E. coli* strains are non-pathogenic; pathogenic strains cause disease primarily through fecal-oral transmission.

Answer: True

While many *E. coli* strains are commensal, pathogenic strains exist and are transmitted via the fecal-oral route, causing various illnesses.

Related Concepts:

  • How can *E. coli* be transmitted, and what makes it a useful indicator organism?: *E. coli* is expelled into the environment in fecal matter. Pathogenic strains can cause disease through fecal-oral transmission, often linked to food contamination. Because cells can survive outside the body for a limited time, *E. coli* serves as an indicator organism to test environmental samples for fecal contamination.
  • What types of diseases can virulent *E. coli* strains cause?: Virulent *E. coli* strains can cause a range of diseases, including gastroenteritis, urinary tract infections (UTIs), neonatal meningitis, hemorrhagic colitis, and can be associated with Crohn's disease. In more severe cases, they can lead to complications like hemolytic-uremic syndrome (HUS), peritonitis, mastitis, sepsis, and pneumonia.
  • When does *E. coli* typically colonize a newborn's gastrointestinal tract, and what is its role there?: *E. coli* usually colonizes an infant's gastrointestinal tract within 40 hours of birth, acquired from the environment or caregivers. In the large intestine, it adheres to the mucus and functions as the primary facultative anaerobe, remaining a benign commensal unless it acquires virulence factors.

*E. coli* serves as an indicator organism because its presence in environmental samples can signify fecal contamination, as it survives outside the host for a limited period.

Answer: True

*E. coli*'s ability to survive in the environment for a time makes it a reliable indicator of fecal contamination in water and food sources.

Related Concepts:

  • How can *E. coli* be transmitted, and what makes it a useful indicator organism?: *E. coli* is expelled into the environment in fecal matter. Pathogenic strains can cause disease through fecal-oral transmission, often linked to food contamination. Because cells can survive outside the body for a limited time, *E. coli* serves as an indicator organism to test environmental samples for fecal contamination.

Strain-specific characteristics of *E. coli* are not useful for identifying the source of fecal contamination in environmental samples.

Answer: False

The unique characteristics of different *E. coli* strains, such as host specificity, are indeed valuable for tracing the origin of fecal contamination in environmental contexts.

Related Concepts:

  • How can the strain-specific characteristics of *E. coli* be used to identify the source of contamination?: Different strains of *E. coli* can possess unique characteristics, such as pathogenicity, the ability to utilize specific carbon sources, or resistance to antimicrobials. Their host specificity allows researchers to determine the origin of fecal contamination in environmental samples, for instance, by identifying whether contamination originated from humans, other mammals, or birds.

What types of diseases can virulent *E. coli* strains cause?

Answer: Gastroenteritis, UTIs, neonatal meningitis, and sepsis.

Virulent strains of *E. coli* are associated with a spectrum of diseases, including gastroenteritis, urinary tract infections, neonatal meningitis, and sepsis.

Related Concepts:

  • What types of diseases can virulent *E. coli* strains cause?: Virulent *E. coli* strains can cause a range of diseases, including gastroenteritis, urinary tract infections (UTIs), neonatal meningitis, hemorrhagic colitis, and can be associated with Crohn's disease. In more severe cases, they can lead to complications like hemolytic-uremic syndrome (HUS), peritonitis, mastitis, sepsis, and pneumonia.
  • What are some of the pathogenic strains of *E. coli* and the diseases they cause?: Pathogenic strains include Enterotoxigenic *E. coli* (ETEC), Enteroinvasive *E. coli* (EIEC), Enterohemorrhagic *E. coli* (EHEC), and specific serotypes like O157:H7 and O104:H4. EHEC and O104:H4 are associated with hemolytic-uremic syndrome (HUS).

How does Shiga toxin produced by *E. coli* O157:H7 lead to severe illness?

Answer: It causes inflammation and destroys red blood cells, potentially leading to kidney damage.

Shiga toxin from *E. coli* O157:H7 induces inflammation and hemolysis, which can obstruct kidney filtration and result in hemolytic-uremic syndrome (HUS).

Related Concepts:

  • How does Shiga toxin produced by some *E. coli* strains lead to severe illness?: Shiga toxin, produced by strains like O157:H7, causes inflammatory responses in the gut, leading to bloody diarrhea. It can also destroy red blood cells, leading to kidney damage and potentially fatal hemolytic-uremic syndrome (HUS) by clogging the kidneys' filtering system.

What is the primary mode of transmission for Enterotoxigenic *E. coli* (ETEC)?

Answer: Contaminated food or drinking water

Enterotoxigenic *E. coli* (ETEC) is typically transmitted through the ingestion of contaminated food or water.

Related Concepts:

  • What is Enterotoxigenic *E. coli* (ETEC), and what is its primary mode of transmission?: Enterotoxigenic *E. coli* (ETEC) is the most common cause of traveler's diarrhea worldwide, particularly affecting children in developing countries. It is typically transmitted through contaminated food or drinking water, adhering to the intestinal lining and secreting enterotoxins that cause watery diarrhea.

Why is Carbapenem-resistant *E. coli* (CREC) a significant concern in healthcare?

Answer: It produces an enzyme that inactivates carbapenem antibiotics, drugs of last resort.

Carbapenem-resistant *E. coli* (CREC) poses a major threat due to its resistance to carbapenems, critical last-resort antibiotics, conferred by carbapenemase enzymes.

Related Concepts:

  • What is carbapenem-resistant *E. coli* (CREC), and why is it a concern?: Carbapenem-resistant *E. coli* (CREC) is a strain of *E. coli* that is resistant to carbapenem antibiotics, which are considered drugs of last resort. This resistance is due to the production of an enzyme called carbapenemase, which inactivates the antibiotic molecule, making infections difficult to treat.

What is the typical incubation period for Shiga toxin-producing *E. coli* (STEC) infections?

Answer: 3-4 days (ranging from 1 to 10 days)

The incubation period for STEC infections typically ranges from 1 to 10 days, with an average of 3 to 4 days.

Related Concepts:

  • What is the typical incubation period for Shiga toxin-producing *E. coli* (STEC) infections?: The incubation period for STEC infections, the time between ingesting the bacteria and feeling sick, is usually 3 to 4 days but can range from 1 day to as long as 10 days. Hemolytic-uremic syndrome (HUS), if it occurs, typically develops about 7 days after the initial symptoms appear, often as the diarrhea begins to improve.

Which diagnostic method is described as faster and offering higher sensitivity and specificity for *E. coli* infections compared to traditional stool cultures?

Answer: Point-of-care molecular diagnostic tests

Point-of-care molecular diagnostic tests offer a more rapid and sensitive approach for identifying *E. coli* infections and associated resistance markers compared to conventional methods.

Related Concepts:

  • How are infectious diarrhea and antimicrobial resistance typically diagnosed in *E. coli* infections?: Diagnosis usually involves a stool culture followed by antibiotic sensitivity testing, which can take from two days to several weeks. Newer point-of-care molecular diagnostic tests can identify *E. coli* and its antimicrobial resistance genes much faster, often within two hours, offering higher sensitivity and specificity.

What is the primary treatment focus for most *E. coli* infections?

Answer: Assessing and replacing lost fluids and electrolytes.

Management of *E. coli* infections primarily involves supportive care, focusing on rehydration and electrolyte balance, as antibiotic use is often reserved or guided by resistance patterns.

Related Concepts:

  • What is the primary treatment for *E. coli* infections, and what role do antibiotics play?: The primary treatment for *E. coli* infections focuses on assessing and replacing lost fluids and electrolytes to combat dehydration. While antibiotics can shorten the illness duration for some *E. coli* types like ETEC, their use is generally not recommended due to increasing resistance, and the choice of antibiotic depends on regional susceptibility patterns.

What is the current status of vaccine development for ETEC?

Answer: Several candidates are in various stages of clinical testing, but no licensed vaccines exist.

While vaccine candidates for enterotoxigenic *E. coli* (ETEC) are undergoing clinical trials, no licensed vaccines are currently available.

Related Concepts:

  • What is the current status of vaccine development for *E. coli*, particularly for ETEC?: Vaccine development is primarily focused on enterotoxigenic *E. coli* (ETEC). While antibodies against ETEC toxins offer protection, there are currently no licensed vaccines for ETEC, although several candidates are in various stages of clinical testing.

Which of the following is an example of an intestinal anti-inflammatory agent, excluding corticosteroids?

Answer: Sulfasalazine

Sulfasalazine is an aminosalicylate used as an intestinal anti-inflammatory agent, distinct from corticosteroid treatments.

Related Concepts:

  • What types of intestinal anti-inflammatory agents are used, excluding corticosteroids?: Besides corticosteroids, intestinal anti-inflammatory agents include antiallergic drugs like cromoglicic acid and aminosalicylates such as sulfasalazine, mesalazine, olsalazine, and balsalazide.

*E. coli* Genetics, Evolution, and Diversity

*E. coli* adapts genetically primarily through vertical gene transfer and mutation.

Answer: False

*E. coli* undergoes significant genetic adaptation through horizontal gene transfer (HGT) mechanisms, in addition to mutation and vertical gene transfer.

Related Concepts:

  • How does *E. coli* facilitate genetic adaptation and the spread of traits like toxin production?: *E. coli* adapts genetically through horizontal gene transfer mechanisms such as bacterial conjugation and transduction. Transduction, mediated by bacteriophages, is particularly significant as it can transfer genes, like the one for Shiga toxin, from other bacteria (e.g., *Shigella*) to *E. coli*, leading to the emergence of pathogenic strains like *E. coli* O157:H7.
  • What are the primary mechanisms driving the evolution of new *E. coli* strains?: New *E. coli* strains evolve through natural biological processes including mutation, gene duplication, and horizontal gene transfer. For instance, approximately 18% of the genome of the laboratory strain MG1655 was acquired horizontally since its divergence from *Salmonella*.
  • How much genetic variation exists among different *E. coli* isolates, and what is the size of the *E. coli* pangenome?: Comparison of *E. coli* genomes shows significant diversity, with only about 20% of genes being shared across all isolates. The total number of different genes found across all sequenced *E. coli* strains, known as the pangenome, exceeds 16,000. It is estimated that two-thirds of this pangenome originated from other species via horizontal gene transfer.

Only about 20% of genes in a typical *E. coli* genome are shared among all strains, indicating significant genetic diversity.

Answer: True

The core genome shared by all *E. coli* strains is small, with approximately 80% of the genome exhibiting variation, highlighting substantial genetic diversity.

Related Concepts:

  • What is the extent of genetic diversity within the *E. coli* species?: *E. coli* exhibits a very high degree of genetic and phenotypic diversity. Only about 20% of the genes in a typical *E. coli* genome are shared among all strains, meaning that approximately 80% of the genome can vary significantly between different isolates.
  • How much genetic variation exists among different *E. coli* isolates, and what is the size of the *E. coli* pangenome?: Comparison of *E. coli* genomes shows significant diversity, with only about 20% of genes being shared across all isolates. The total number of different genes found across all sequenced *E. coli* strains, known as the pangenome, exceeds 16,000. It is estimated that two-thirds of this pangenome originated from other species via horizontal gene transfer.
  • What are the primary mechanisms driving the evolution of new *E. coli* strains?: New *E. coli* strains evolve through natural biological processes including mutation, gene duplication, and horizontal gene transfer. For instance, approximately 18% of the genome of the laboratory strain MG1655 was acquired horizontally since its divergence from *Salmonella*.

The concept of "taxa in disguise" suggests that *Shigella* species are genetically very different from *E. coli*.

Answer: False

The concept of "taxa in disguise" indicates that *Shigella* species are phylogenetically nested within *E. coli*, suggesting they are genetically very similar, not different.

Related Concepts:

  • What is the concept of "taxa in disguise" as it relates to *E. coli* and *Shigella*?: The concept of "taxa in disguise" refers to the observation that certain bacteria, like the species within the genus *Shigella* (*S. dysenteriae*, *S. flexneri*, *S. boydii*, and *S. sonnei*), are so genetically similar to *E. coli* strains that they should, from a phylogenetic perspective, be classified as *E. coli* strains. This highlights the blurred lines in bacterial taxonomy due to horizontal gene transfer and evolutionary proximity.
  • What is the relationship between *E. coli* and *Shigella* from a phylogenetic perspective?: Phylogenetically, the four species of *Shigella* are nested within *E. coli* strains. A phylogenomic study that included the type strain placed all *Shigella* species within a single subspecies of *E. coli*, suggesting a close evolutionary relationship.

*E. coli* strains are commonly subdivided by their metabolic pathways, such as fermentation types.

Answer: False

*E. coli* strains are primarily subdivided based on serotype, determined by surface antigens (O, H, and K antigens), rather than metabolic pathways.

Related Concepts:

  • What are the primary metabolic capabilities of *E. coli* under anaerobic conditions?: Under anaerobic conditions, *E. coli* utilizes mixed acid fermentation, producing byproducts such as lactate, succinate, ethanol, acetate, and carbon dioxide. This process requires low levels of hydrogen gas, often achieved when *E. coli* coexists with hydrogen-consuming organisms like methanogens or sulfate-reducing bacteria.
  • How can the strain-specific characteristics of *E. coli* be used to identify the source of contamination?: Different strains of *E. coli* can possess unique characteristics, such as pathogenicity, the ability to utilize specific carbon sources, or resistance to antimicrobials. Their host specificity allows researchers to determine the origin of fecal contamination in environmental samples, for instance, by identifying whether contamination originated from humans, other mammals, or birds.
  • How are *E. coli* strains commonly subdivided, and what do these subdivisions represent?: *E. coli* strains are commonly subdivided by serotype, which is based on major surface antigens. These antigens include the O antigen (part of the lipopolysaccharide layer), the H antigen (flagellin), and the K antigen (capsule). For example, O157:H7 is a well-known serotype. Often, only the serogroup, identified by the O-antigen, is cited, with approximately 190 known serogroups.

The Red Queen hypothesis describes how *E. coli* evolves to maintain its fitness in response to its predators' adaptations.

Answer: True

The Red Queen hypothesis applies to *E. coli*'s co-evolutionary arms race with its predators, where continuous adaptation is necessary for survival.

Related Concepts:

  • How does the Red Queen hypothesis apply to the co-evolutionary relationship between *E. coli* and its predators?: The Red Queen hypothesis describes a co-evolutionary dynamic where *E. coli*, as prey to predators like *Myxococcus xanthus*, undergoes genomic and phenotypic modifications to adapt. These adaptations, such as mucoid production or suppression of certain genes, are countered by the predator's evolution, creating an ongoing evolutionary arms race where both species must continuously adapt to survive.

Phylogenetic classification of *E. coli* shows a strong link between phylogenetic distance and pathology, meaning closely related strains are always equally pathogenic.

Answer: False

While phylogeny can indicate relationships, the link between phylogenetic distance and pathogenicity in *E. coli* is not always direct or uniform; closely related strains can exhibit varying levels of pathogenicity.

Related Concepts:

  • How are *E. coli* strains classified phylogenetically, and what are the implications for pathology?: *E. coli* strains can be classified according to their phylogeny, or inferred evolutionary history, with species divided into groups. While whole genome sequencing yields robust phylogenies, the link between phylogenetic distance and pathology is often small. For example, strains within the O157:H7 clade (Group E) are all enterohaemorrhagic (EHEC), but not all EHEC strains are closely related.

The first complete genome sequence of *E. coli*, published in 1997, revealed a genome of approximately 4.6 million base pairs.

Answer: True

The initial sequencing of the *E. coli* K-12 genome in 1997 established its size at approximately 4.6 million base pairs.

Related Concepts:

  • What was revealed by the first complete genome sequence of *E. coli*?: The first complete DNA sequence of an *E. coli* genome (strain K-12 derivative MG1655), published in 1997, revealed a circular DNA molecule of 4.6 million base pairs. It contained 4,288 protein-coding genes, organized into operons, along with ribosomal RNA (rRNA) and transfer RNA (tRNA) genes. The genome was found to be densely coded, with a high number of transposable elements, repeat elements, and phage remnants, indicating plasticity through horizontal transfer.
  • What does the genome sequence of *E. coli* predict regarding its proteome, and how many proteins have been experimentally identified?: The *E. coli* genome sequence predicts 4,288 protein-coding genes, with about 38% initially having no attributed function. By 2006, 1,627 (38%) of these predicted proteins had been experimentally identified, and a 2020 study detected 2,586 proteins.
  • How much genetic variation exists among different *E. coli* isolates, and what is the size of the *E. coli* pangenome?: Comparison of *E. coli* genomes shows significant diversity, with only about 20% of genes being shared across all isolates. The total number of different genes found across all sequenced *E. coli* strains, known as the pangenome, exceeds 16,000. It is estimated that two-thirds of this pangenome originated from other species via horizontal gene transfer.

The *E. coli* pangenome, representing all genes found across sequenced strains, is estimated to be around 5,000 genes.

Answer: False

The *E. coli* pangenome is considerably larger than 5,000 genes, estimated to contain over 16,000 genes in total, with a significant portion acquired through horizontal gene transfer.

Related Concepts:

  • How much genetic variation exists among different *E. coli* isolates, and what is the size of the *E. coli* pangenome?: Comparison of *E. coli* genomes shows significant diversity, with only about 20% of genes being shared across all isolates. The total number of different genes found across all sequenced *E. coli* strains, known as the pangenome, exceeds 16,000. It is estimated that two-thirds of this pangenome originated from other species via horizontal gene transfer.
  • What was revealed by the first complete genome sequence of *E. coli*?: The first complete DNA sequence of an *E. coli* genome (strain K-12 derivative MG1655), published in 1997, revealed a circular DNA molecule of 4.6 million base pairs. It contained 4,288 protein-coding genes, organized into operons, along with ribosomal RNA (rRNA) and transfer RNA (tRNA) genes. The genome was found to be densely coded, with a high number of transposable elements, repeat elements, and phage remnants, indicating plasticity through horizontal transfer.
  • What does the genome sequence of *E. coli* predict regarding its proteome, and how many proteins have been experimentally identified?: The *E. coli* genome sequence predicts 4,288 protein-coding genes, with about 38% initially having no attributed function. By 2006, 1,627 (38%) of these predicted proteins had been experimentally identified, and a 2020 study detected 2,586 proteins.

Genes in *E. coli* are typically named using three-letter acronyms, which are italicized, and the corresponding proteins are named with uppercase acronyms.

Answer: True

The standard nomenclature for *E. coli* genes involves italicized three-letter acronyms for genes and uppercase acronyms for their corresponding proteins.

Related Concepts:

  • What is the standard system for naming genes in *E. coli*?: Genes in *E. coli* typically follow a uniform nomenclature system proposed by Demerec et al. Gene names are three-letter acronyms, usually derived from their function or mutant phenotype, and are italicized. Related genes are designated with subsequent letters (e.g., recA, recB), and the corresponding proteins are named with uppercase acronyms (e.g., RecA, RecB).

By 2006, about 38% of the predicted proteins from the *E. coli* genome sequence had been experimentally identified.

Answer: True

Early proteomic studies confirmed a significant portion of the predicted proteins from the *E. coli* genome sequence, with around 38% identified by 2006.

Related Concepts:

  • What does the genome sequence of *E. coli* predict regarding its proteome, and how many proteins have been experimentally identified?: The *E. coli* genome sequence predicts 4,288 protein-coding genes, with about 38% initially having no attributed function. By 2006, 1,627 (38%) of these predicted proteins had been experimentally identified, and a 2020 study detected 2,586 proteins.
  • What was revealed by the first complete genome sequence of *E. coli*?: The first complete DNA sequence of an *E. coli* genome (strain K-12 derivative MG1655), published in 1997, revealed a circular DNA molecule of 4.6 million base pairs. It contained 4,288 protein-coding genes, organized into operons, along with ribosomal RNA (rRNA) and transfer RNA (tRNA) genes. The genome was found to be densely coded, with a high number of transposable elements, repeat elements, and phage remnants, indicating plasticity through horizontal transfer.

How does *E. coli* facilitate genetic adaptation and the spread of traits like toxin production?

Answer: Through horizontal gene transfer mechanisms like conjugation and transduction.

Horizontal gene transfer, including conjugation and transduction, plays a critical role in the genetic adaptation and acquisition of new traits, such as virulence factors, by *E. coli*.

Related Concepts:

  • How does *E. coli* facilitate genetic adaptation and the spread of traits like toxin production?: *E. coli* adapts genetically through horizontal gene transfer mechanisms such as bacterial conjugation and transduction. Transduction, mediated by bacteriophages, is particularly significant as it can transfer genes, like the one for Shiga toxin, from other bacteria (e.g., *Shigella*) to *E. coli*, leading to the emergence of pathogenic strains like *E. coli* O157:H7.
  • What are the primary mechanisms driving the evolution of new *E. coli* strains?: New *E. coli* strains evolve through natural biological processes including mutation, gene duplication, and horizontal gene transfer. For instance, approximately 18% of the genome of the laboratory strain MG1655 was acquired horizontally since its divergence from *Salmonella*.

What is the approximate percentage of genes in a typical *E. coli* genome that are shared among all strains?

Answer: 20%

Only about 20% of the genes in a typical *E. coli* genome are conserved across all strains, indicating substantial genetic diversity.

Related Concepts:

  • What is the extent of genetic diversity within the *E. coli* species?: *E. coli* exhibits a very high degree of genetic and phenotypic diversity. Only about 20% of the genes in a typical *E. coli* genome are shared among all strains, meaning that approximately 80% of the genome can vary significantly between different isolates.
  • How much genetic variation exists among different *E. coli* isolates, and what is the size of the *E. coli* pangenome?: Comparison of *E. coli* genomes shows significant diversity, with only about 20% of genes being shared across all isolates. The total number of different genes found across all sequenced *E. coli* strains, known as the pangenome, exceeds 16,000. It is estimated that two-thirds of this pangenome originated from other species via horizontal gene transfer.
  • What was revealed by the first complete genome sequence of *E. coli*?: The first complete DNA sequence of an *E. coli* genome (strain K-12 derivative MG1655), published in 1997, revealed a circular DNA molecule of 4.6 million base pairs. It contained 4,288 protein-coding genes, organized into operons, along with ribosomal RNA (rRNA) and transfer RNA (tRNA) genes. The genome was found to be densely coded, with a high number of transposable elements, repeat elements, and phage remnants, indicating plasticity through horizontal transfer.

The concept of "taxa in disguise" in relation to *E. coli* and *Shigella* refers to:

Answer: Shigella species being genetically similar to E. coli strains.

The "taxa in disguise" concept highlights the close phylogenetic relationship between *Shigella* and *E. coli*, suggesting *Shigella* should be classified within *E. coli*.

Related Concepts:

  • What is the concept of "taxa in disguise" as it relates to *E. coli* and *Shigella*?: The concept of "taxa in disguise" refers to the observation that certain bacteria, like the species within the genus *Shigella* (*S. dysenteriae*, *S. flexneri*, *S. boydii*, and *S. sonnei*), are so genetically similar to *E. coli* strains that they should, from a phylogenetic perspective, be classified as *E. coli* strains. This highlights the blurred lines in bacterial taxonomy due to horizontal gene transfer and evolutionary proximity.

How are *E. coli* strains commonly subdivided?

Answer: By serotype, based on major surface antigens.

*E. coli* strains are primarily classified and subdivided based on their serotypes, which are determined by variations in their surface antigens (O, H, and K).

Related Concepts:

  • How are *E. coli* strains commonly subdivided, and what do these subdivisions represent?: *E. coli* strains are commonly subdivided by serotype, which is based on major surface antigens. These antigens include the O antigen (part of the lipopolysaccharide layer), the H antigen (flagellin), and the K antigen (capsule). For example, O157:H7 is a well-known serotype. Often, only the serogroup, identified by the O-antigen, is cited, with approximately 190 known serogroups.
  • How are *E. coli* strains classified phylogenetically, and what are the implications for pathology?: *E. coli* strains can be classified according to their phylogeny, or inferred evolutionary history, with species divided into groups. While whole genome sequencing yields robust phylogenies, the link between phylogenetic distance and pathology is often small. For example, strains within the O157:H7 clade (Group E) are all enterohaemorrhagic (EHEC), but not all EHEC strains are closely related.
  • What is the extent of genetic diversity within the *E. coli* species?: *E. coli* exhibits a very high degree of genetic and phenotypic diversity. Only about 20% of the genes in a typical *E. coli* genome are shared among all strains, meaning that approximately 80% of the genome can vary significantly between different isolates.

Which of the following is a key characteristic of the Red Queen hypothesis as applied to *E. coli*?

Answer: E. coli's adaptations are countered by predator evolution, creating an ongoing arms race.

The Red Queen hypothesis describes a scenario where *E. coli* must continuously adapt to counter the evolving adaptations of its predators, leading to a perpetual evolutionary struggle.

Related Concepts:

  • How does the Red Queen hypothesis apply to the co-evolutionary relationship between *E. coli* and its predators?: The Red Queen hypothesis describes a co-evolutionary dynamic where *E. coli*, as prey to predators like *Myxococcus xanthus*, undergoes genomic and phenotypic modifications to adapt. These adaptations, such as mucoid production or suppression of certain genes, are countered by the predator's evolution, creating an ongoing evolutionary arms race where both species must continuously adapt to survive.

What was revealed by the first complete genome sequence of *E. coli* in 1997?

Answer: A genome of 4.6 million base pairs containing 4,288 protein-coding genes.

The first complete genome sequence of *E. coli* (strain K-12) in 1997 revealed a genome of approximately 4.6 million base pairs encoding 4,288 protein-coding genes.

Related Concepts:

  • What was revealed by the first complete genome sequence of *E. coli*?: The first complete DNA sequence of an *E. coli* genome (strain K-12 derivative MG1655), published in 1997, revealed a circular DNA molecule of 4.6 million base pairs. It contained 4,288 protein-coding genes, organized into operons, along with ribosomal RNA (rRNA) and transfer RNA (tRNA) genes. The genome was found to be densely coded, with a high number of transposable elements, repeat elements, and phage remnants, indicating plasticity through horizontal transfer.
  • How much genetic variation exists among different *E. coli* isolates, and what is the size of the *E. coli* pangenome?: Comparison of *E. coli* genomes shows significant diversity, with only about 20% of genes being shared across all isolates. The total number of different genes found across all sequenced *E. coli* strains, known as the pangenome, exceeds 16,000. It is estimated that two-thirds of this pangenome originated from other species via horizontal gene transfer.
  • How has *E. coli* contributed to our understanding of fundamental biological processes?: *E. coli* has been instrumental in understanding key biological processes. It was used to first describe bacterial conjugation by Lederberg and Tatum, and its study with bacteriophages by researchers like Seymour Benzer helped elucidate the topography of gene structure. Its genome was also among the first to be sequenced, providing a foundational resource for molecular biology.

What is the *E. coli* pangenome?

Answer: The total number of different genes found across all sequenced *E. coli* strains.

The *E. coli* pangenome encompasses the complete set of genes present in all known strains of the species.

Related Concepts:

  • How much genetic variation exists among different *E. coli* isolates, and what is the size of the *E. coli* pangenome?: Comparison of *E. coli* genomes shows significant diversity, with only about 20% of genes being shared across all isolates. The total number of different genes found across all sequenced *E. coli* strains, known as the pangenome, exceeds 16,000. It is estimated that two-thirds of this pangenome originated from other species via horizontal gene transfer.

What is the standard system for naming genes in *E. coli*?

Answer: Three-letter acronyms, italicized for genes and uppercase for proteins.

The established nomenclature for *E. coli* genes uses italicized three-letter acronyms for genes and uppercase acronyms for the corresponding proteins.

Related Concepts:

  • What is the standard system for naming genes in *E. coli*?: Genes in *E. coli* typically follow a uniform nomenclature system proposed by Demerec et al. Gene names are three-letter acronyms, usually derived from their function or mutant phenotype, and are italicized. Related genes are designated with subsequent letters (e.g., recA, recB), and the corresponding proteins are named with uppercase acronyms (e.g., RecA, RecB).

What is the relationship between *E. coli* and *Shigella* from a phylogenetic perspective?

Answer: Shigella species are nested within E. coli strains.

Phylogenetic analyses indicate that *Shigella* species are closely related to and nested within *E. coli* strains.

Related Concepts:

  • What is the relationship between *E. coli* and *Shigella* from a phylogenetic perspective?: Phylogenetically, the four species of *Shigella* are nested within *E. coli* strains. A phylogenomic study that included the type strain placed all *Shigella* species within a single subspecies of *E. coli*, suggesting a close evolutionary relationship.
  • How are *E. coli* strains classified phylogenetically, and what are the implications for pathology?: *E. coli* strains can be classified according to their phylogeny, or inferred evolutionary history, with species divided into groups. While whole genome sequencing yields robust phylogenies, the link between phylogenetic distance and pathology is often small. For example, strains within the O157:H7 clade (Group E) are all enterohaemorrhagic (EHEC), but not all EHEC strains are closely related.

What is the *E. coli* pangenome estimated to contain, and what is the origin of a significant portion of it?

Answer: Over 16,000 genes, with two-thirds originating from horizontal gene transfer.

The *E. coli* pangenome is vast, estimated at over 16,000 genes, with a substantial fraction acquired through horizontal gene transfer from other species.

Related Concepts:

  • How much genetic variation exists among different *E. coli* isolates, and what is the size of the *E. coli* pangenome?: Comparison of *E. coli* genomes shows significant diversity, with only about 20% of genes being shared across all isolates. The total number of different genes found across all sequenced *E. coli* strains, known as the pangenome, exceeds 16,000. It is estimated that two-thirds of this pangenome originated from other species via horizontal gene transfer.
  • What was revealed by the first complete genome sequence of *E. coli*?: The first complete DNA sequence of an *E. coli* genome (strain K-12 derivative MG1655), published in 1997, revealed a circular DNA molecule of 4.6 million base pairs. It contained 4,288 protein-coding genes, organized into operons, along with ribosomal RNA (rRNA) and transfer RNA (tRNA) genes. The genome was found to be densely coded, with a high number of transposable elements, repeat elements, and phage remnants, indicating plasticity through horizontal transfer.
  • What is the extent of genetic diversity within the *E. coli* species?: *E. coli* exhibits a very high degree of genetic and phenotypic diversity. Only about 20% of the genes in a typical *E. coli* genome are shared among all strains, meaning that approximately 80% of the genome can vary significantly between different isolates.

Specific Strains and Their Applications

The neotype strain for *E. coli* is U5/41^T, but common laboratory strains like K-12 MG1655 are not used in studies.

Answer: False

While U5/41^T is the neotype strain, common laboratory strains such as K-12 MG1655 are extensively used in research studies.

Related Concepts:

  • What are some specific laboratory strains of *E. coli* and their uses?: Several *E. coli* strains are widely used in labs: K-12 derivatives like DH1, DH5α, MG1655, and W3110 are common in biotechnology. Strain Nissle 1917 is used as a probiotic. Strain OP50 is used for maintaining *Caenorhabditis elegans* cultures. Strain JM109, deficient in recA and endA, is useful for cloning and expression systems.
  • Which *E. coli* groups do most commonly used research strains belong to?: Most commonly used research strains of *E. coli*, such as those derived from Clifton's K-12 strain or d'Herelle's B strain, belong to Group A.
  • What is the significance of the neotype strain for *E. coli*, and which strains are commonly used in research?: The original strain described by Theodor Escherich is believed to be lost, so a new type strain, known as the neotype strain U5/41^T (also designated DSM 30083, ATCC 11775, and NCTC 9001), was chosen as a representative. However, in most studies, common laboratory strains like O157:H7, K-12 MG1655, or K-12 W3110 are used.

Most commonly used research strains of *E. coli*, such as Clifton's K-12 strain, belong to Phylogenetic Group A.

Answer: True

Research strains derived from K-12 and other common laboratory strains are typically classified under Phylogenetic Group A.

Related Concepts:

  • Which *E. coli* groups do most commonly used research strains belong to?: Most commonly used research strains of *E. coli*, such as those derived from Clifton's K-12 strain or d'Herelle's B strain, belong to Group A.

Which *E. coli* strain is specifically mentioned as being used for maintaining cultures of the nematode *Caenorhabditis elegans*?

Answer: E. coli OP50

*E. coli* strain OP50 is commonly used as a food source for maintaining cultures of the nematode *Caenorhabditis elegans*.

Related Concepts:

  • What are some specific laboratory strains of *E. coli* and their uses?: Several *E. coli* strains are widely used in labs: K-12 derivatives like DH1, DH5α, MG1655, and W3110 are common in biotechnology. Strain Nissle 1917 is used as a probiotic. Strain OP50 is used for maintaining *Caenorhabditis elegans* cultures. Strain JM109, deficient in recA and endA, is useful for cloning and expression systems.

What is Uropathogenic *E. coli* (UPEC)?

Answer: A major cause of urinary tract infections (UTIs).

Uropathogenic *E. coli* (UPEC) is a significant etiological agent responsible for the majority of urinary tract infections.

Related Concepts:

  • What is Uropathogenic *E. coli* (UPEC), and how does it cause urinary tract infections?: Uropathogenic *E. coli* (UPEC) is a major cause of urinary tract infections (UTIs). Although it normally resides in the gut, it can be introduced into the urinary tract through various means, particularly in females through improper wiping techniques or in males and females via sexual contact, leading to infection.

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