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Ch. 18 - Control of Gene Expression in Bacteria
Freeman - Biological Science 8th Edition
Freeman8th EditionBiological ScienceISBN: 9780138276263Not the one you use?Change textbook
Chapter 18, Problem 13

The diagram shown here is a model of the gene regulatory circuit for light production by V. fischeri cells. The lux operon contains genes for luminescence (luxCDABE) and a gene, luxI, that encodes an enzyme that catalyzes the production of an inducer. This inducer easily moves back and forth across the plasma membrane and acts as a signaling molecule. The lux operon is never completely turned off. The luxR gene codes for the activator LuxR. The inducer can bind to LuxR, and when it does, the LuxR–inducer complex can bind to a regulatory site to activate transcription of the lux operon and inhibit transcription of luxR.
Explain how this gene regulatory circuit accounts for bacteria emitting light only when they reach a high cell density.

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1
Understand the concept of quorum sensing: Quorum sensing is a mechanism by which bacteria communicate and coordinate behavior based on their population density. In this case, V. fischeri uses quorum sensing to regulate light production.
Identify the role of the inducer: The inducer is a signaling molecule produced by the enzyme encoded by the luxI gene. This inducer can diffuse across the plasma membrane and accumulate both inside and outside the cell.
Explain the accumulation of the inducer: At low cell density, the concentration of the inducer is low because it diffuses away into the environment. However, as the bacterial population increases, the concentration of the inducer in the environment also increases, leading to a higher concentration of the inducer inside the cells.
Describe the activation of the lux operon: When the inducer concentration reaches a threshold level, it binds to the LuxR protein, forming the LuxR–inducer complex. This complex binds to the regulatory site of the lux operon, activating its transcription. This leads to the production of luminescence genes (luxCDABE) and more inducer (positive feedback).
Explain the high cell density requirement: The system ensures that light production only occurs at high cell density because the inducer concentration must reach a critical threshold to activate the lux operon. This prevents energy waste by producing light only when there are enough bacteria to make the light visible.

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Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Quorum Sensing

Quorum sensing is a communication mechanism used by bacteria to coordinate behavior based on population density. When the cell density is high, the concentration of signaling molecules, such as the inducer produced by luxI, increases. This allows bacteria to collectively regulate gene expression, such as the lux operon, leading to behaviors like bioluminescence only when a sufficient number of cells are present.
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Lux Operon

The lux operon is a set of genes in V. fischeri that are responsible for bioluminescence. It includes genes that encode proteins necessary for light production (luxCDABE) and the luxI gene, which produces an inducer. The operon is regulated by the LuxR protein, which, when activated by the inducer, enhances the transcription of the lux genes, allowing the bacteria to emit light in response to high cell density.
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Feedback Inhibition

Feedback inhibition is a regulatory mechanism where the product of a process inhibits its own production. In the context of the lux operon, when the LuxR–inducer complex activates the transcription of the lux operon, it simultaneously inhibits the transcription of luxR. This ensures that as luminescence increases, the production of the activator LuxR decreases, creating a balance that prevents overexpression of the luminescent genes.
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Related Practice
Textbook Question

X-gal is a colorless, lactose-like molecule that can be split into two fragments by ββ-galactosidase. One of these product molecules creates a blue color. The photograph here shows E. coli colonies growing in a medium that contains X-gal. Find three colonies whose cells have functioning copies of ββ-galactosidase.

Find three colonies whose cells might have mutations in the lacZ or the lacY genes.

Suppose you analyze the protein-coding sequence of the lacZ and lacY genes of cells from the three mutant colonies and find that these sequences are wild type (normal).

What other region of the lac operon might be altered to account for the mutant phenotype of these colonies?

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Textbook Question

The Hawaiian bobtail squid (Euprymna scolopes) is able to glow from luminescent Vibrio fischeri bacteria held in its light organs. As it swims at night near the ocean surface, it adjusts the amount of light visible to predators below to match the light from the stars and moon. Predators have difficulty seeing the illuminated squid against the night sky.

The bacteria glow in response to a molecule that regulates expression of genes involved in light-producing chemical reactions. The regulator controls production of the genes' mRNA. Therefore, the light-producing genes are under

a. Transcriptional control.

b. Translational control.

c. Post-translational control.

d. Negative control.

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Textbook Question

The light-producing genes of V. fischeri are organized in an operon that is under positive control by an activator protein called LuxR.

Would you expect the genes of this operon to be transcribed when LuxR is bound or not bound to a DNA regulatory sequence? Explain.

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Textbook Question

LuxR is allosterically regulated by the inducer molecule secreted by V. fischeri.

What does it mean that LuxR is allosterically regulated?

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Textbook Question

What characteristic of the light-producing regulatory circuit is consistent with the idea that it may be a regulon?

What characteristic of this circuit stretches the definition for a regulon?

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Textbook Question

Quorum sensing (introduced in Ch. 11, Section 11.4) allows bacteria to detect the number of neighboring cells and to trigger a response only when this number reaches a critical level. Quorum sensing is used by V. fischeri in light production and by many pathogenic bacteria, including Vibrio cholerae, to turn on genes for toxin production only when a critical cell density is reached.

Why might quorum sensing be beneficial to pathogenic bacteria?

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