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Describe the role of attenuation in the regulation of tryptophan biosynthesis.

Short Answer

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Answer: Attenuation is a crucial regulatory mechanism in tryptophan biosynthesis that acts as a feedback mechanism to control the expression of the trp operon genes. It ensures that the bacterial cell produces tryptophan only when it is needed, by responding to the availability of tryptophan in the cell. This preserves cellular resources and maintains optimal cellular function.

Step by step solution

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1. Defining Attenuation

Attenuation is a regulatory mechanism that controls the synthesis of specific proteins in bacteria. It is a premature termination of transcription that occurs when the specific conditions are met. Attenuation involves a series of events, including the formation of secondary structures in the mRNA molecule, which affects transcription. It is a crucial mechanism for regulating gene expression in response to the cellular environment.
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2. The role of tryptophan in bacterial cells

Tryptophan is an essential amino acid required for protein synthesis in bacterial cells. It can either be obtained from the environment or synthesized by the cell itself. The genes responsible for tryptophan biosynthesis are organized in a cluster called the trp operon. The trp operon is regulated by various mechanisms, including attenuation, to ensure that the cell produces tryptophan only when it is needed.
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3. Functional detail of attenuation in tryptophan biosynthesis

In the regulation of tryptophan biosynthesis, attenuation acts as a feedback mechanism to control the expression of the trp operon. During transcription, a selective regulatory region called the leader sequence is transcribed before the structural genes of the trp operon. The leader sequence contains a series of tryptophan codons, followed by an attenuator sequence that can form two alternative secondary structures in the mRNA molecule: an anti-terminator and a terminator structure.
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4. The attenuation mechanism based on tryptophan availability

When tryptophan levels are low, ribosome translation of the leader sequence is stalled at the tryptophan codons because there is not enough charged tRNA with tryptophan to continue translation. As a result, the anti-terminator structure forms in the mRNA, allowing transcription to continue and the expression of trp operon genes to produce enzymes responsible for tryptophan biosynthesis. If tryptophan levels are high, there is enough tRNA with tryptophan to continue translation, and the ribosome reaches the attenuator sequence. The presence of the ribosome promotes the formation of the terminator structure in the mRNA, which stops further transcription and prevents the expression of trp operon genes, thus conserving cellular resources and preventing excess tryptophan synthesis.
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5. Conclusion: Importance of attenuation in tryptophan biosynthesis

Attenuation plays a vital role in the regulation of tryptophan biosynthesis by acting as a feedback mechanism that responds to the availability of tryptophan. By controlling the expression of the trp operon genes, attenuation ensures that the cell produces tryptophan only when it is needed, preserving resources and maintaining optimal cellular function.

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In the publication that provided the first evidence of CRISPRCas as an adaptive immune system [Barrangou, R., et al. (2007). Science. \(315: 1709-1712\) ], the authors state that CRISPR-Cas "provides a historical perspective of phage exposure, as well as a predictive tool for phage sensitivity." Explain how this is true using what you know about the CRISPR locus.

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In this chapter, we focused on the regulation of gene expression in bacteria. Along the way, we found many opportunities to consider the methods and reasoning by which much of this information was acquired. From the explanations given in the chapter, what answers would you propose to the following fundamental questions? (a) How do we know that bacteria regulate the expression of certain genes in response to the environment? (b) What evidence established that lactose serves as the inducer of a gene whose product is related to lactose metabolism? (c) What led researchers to conclude that a repressor molecule regulates the lac operon? (d) How do we know that the lac repressor is a protein? (e) How do we know that the trp operon is a repressible control system, in contrast to the lac operon, which is an inducible control system?

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