Biology
12th Edition
ISBN: 9780078024269
Author: Sylvia Mader, Michael Windelspecht
Publisher: McGraw-Hill Education
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Chapter 39, Problem 4A
Summary Introduction
Introduction:
The human skeletal system is the support system of the vertebrates. In human there are aroundbones in adult. The skeletal system of humans is divided into the axial skeleton and the appendicular skeleton.
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a) State the Central Dogma of Molecular Biology in your own words.
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a) The lux operon is under positive control. Based on this information, does the luxR regulator sequence make a repressor protein or an activator protein?
b) How will binding of this complex affect RNA polymerase? Remember this operon is under positive control.
c) AHL is a signal molecule that V. fisheri makes to communicate with neighboring bacterial cells. This molecule can diffuse outside of the cell and into another bacterial cell in close proximity. This type of communication between bacterial cells is known as quorum sensing. If bacterial cell density is low how will this affect the lux operon? What will happen if the density is high?
Chapter 39 Solutions
Biology
Ch. 39.1 - Prob. 1CYPCh. 39.1 - Prob. 2CYPCh. 39.1 - Prob. 3CYPCh. 39.2 - Describe the functions of osteoblasts,...Ch. 39.2 - Prob. 2CYPCh. 39.2 - Prob. 3CYPCh. 39.3 - Define an antagonistic pair of muscles.Ch. 39.3 - Describe the microscopic levels of structure in a...Ch. 39.3 - Prob. 3CYPCh. 39 - Prob. 1A
Ch. 39 - Prob. 2ACh. 39 - Prob. 3ACh. 39 - Prob. 4ACh. 39 - Prob. 5ACh. 39 - Prob. 6ACh. 39 - Prob. 7ACh. 39 - Prob. 8ACh. 39 - Prob. 9ACh. 39 - Prob. 10ACh. 39 - Prob. 11ACh. 39 - Prob. 12ACh. 39 - According to the sliding filament model, when...Ch. 39 - Prob. 14ACh. 39 - Prob. 15ACh. 39 - Prob. 16ACh. 39 - Prob. 1TSCh. 39 - Prob. 2TSCh. 39 - Prob. 3TSCh. 39 - Prob. 4TS
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- a) The relationship between the Hawaiian bobtail squid and V. fischeri is symbiotic where both species benefit. What is the benefit to each? b) Why might quorum sensing be beneficial to pathogenic bacteria? c) How might scientists use quorum sensing to treat bacterial infections?arrow_forwarda) What is the function of the disulfide bonds that form within and between the alpha and beta chains? b) How does proinsulin differ from mature insulin? c) What organelles are involved in forming mature insulin?arrow_forwarda) The amino acid sequence of the alpha chain terminates with a *. What does this symbol mean? b) In your own words describe the function of the signal peptide and its final fate in post transcriptional modification. c)How many amino acids form the precursor of insulin (preproinsulin)? d) Since the C-peptide is cut out of proinsulin to create the final mature insulin (B-chain and A-chain) what role do you think the C-peptide might play in the biosynthesis of the mature insulin protein?arrow_forward
- a) Calculating Transformation Efficiency For the +DNA/+Amp/+IPTG plate, record the following: Number of transformants (colonies): _________________ Nanograms of plasmid DNA added: 50 ng Final recovery volume: 0.50 mL Volume plated: 0.25 mL Transformation efficiency equation: Transformation efficiency = Number of transformants / µg of DNA x Final volume at recovery (mL)/ volume plated (mL) b) Using the equation above, calculate the transformation efficiency. c) Describe the success of the transformation efficiency of this demo based on the calculation you did above?arrow_forwarda) What differences would you expect to see between the -DNA/+Amp and +DNA/+Amp plates? b) Predict the growth you would expect to see on each of the following plates: – DNA ___________________________________________________________ – DNA/+Amp ______________________________________________________ +DNA/+Amp ______________________________________________________ +DNA/+Amp/+IPTG _________________________________________________arrow_forward1)Which plate did you see purple/pink/blue bacterial cells? Why did you see this growth? Explain your answer in terms of transformation and plasmids? 2) Calculating Transformation Efficiency For the +DNA/+Amp/+IPTG plate, record the following: Number of transformants (colonies): _________________ Nanograms of plasmid DNA added: 50 ng Final recovery volume: 0.50 mL Volume plated: 0.25 mL Transformation efficiency equation: Transformation efficiency = Number of transformants / µg of DNA x Final volume at recovery (mL)/ volume plated (mL) 3) Using the equation above, calculate the transformation efficiency. 4) Describe the success of the transformation efficiency of this demo based on the calculation you did above?arrow_forward
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