Exam 12: Bio-techniques and Synthetic Biology

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The following is a potential application of bacterial oscillator switches:

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The migration of linear DNA molecules in agarose or polyacrylamide gels occurs at a rate that is:

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Once a gene encoding a putative transcriptional regulatory protein is identified by sequence annotation, what needs to be done to demonstrate this activity?

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Describe the use of a primary and secondary antibody in a western blot.

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Sigma B is a stress-induced transcription factor in Bacillus subtilis. Bacteria producing a sigma B-YFP fusion protein were exposed to constant energy stress and fluorescence pulses emitted by individual cells were detected by time-lapse microscopy. Could this result have been obtained using a sigma B- β\beta -gal fusion protein?

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What is synthetic biology? Provide an example of its potential applications.

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The genes for proteins such as β\beta -galactosidase (lacZ) or green fluorescent protein (gfp) can be fused to the promoter of a gene of interest. Which of the following statements is NOT correct about gfp and lacZ?

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Describe the whole-genome DNA-binding analysis using ChIP-on-chip technology.

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What hybridization technique can be used to confirm if two genes are components of an operon by estimating transcript size?

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DNA fragments with specific sequences are detected by a technique known as:

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The electrophoretic mobility shift assay (EMSA) is utilized to monitor molecular interactions between:

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What is the basis for the use of the Bt toxin as an insecticide? What are some of the beneficial aspects of using Bt?

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Both Southern and northern blots involve the use of agarose gels. How do the types of agarose gels differ and why?

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How do operon fusions reveal transcriptional control of a target gene?

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In the yeast two-hybrid analysis technique, in vivo protein-protein interactions are explored. The "bait" and "prey" proteins are translationally fused to the cleaved activation and DNA-binding domains of the GAL4 transcription factor. What is the target gene of GAL4?

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The first historical record of biotechnology was:

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How can a single northern blot reveal differences in size and abundance of the E. coli acid resistance gene gadA with respect to the gadBC operon and the inducible expression of these genes at low pH?

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Briefly explain how real-time polymerase chain reaction (PCR) works.

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How can a protein be detected on a western blot?

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What are translational fusions used for? How are they constructed?

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