Connect With Learnsmart Labs Online Access For Prescott's Microbiology
11th Edition
ISBN: 9781260408997
Author: Joanne Willey
Publisher: Mcgraw-hill Higher Education (us)
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Chapter 24.1, Problem 7CC
Why has taxonomic classification of protists been problematic?
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Chapter 24 Solutions
Connect With Learnsmart Labs Online Access For Prescott's Microbiology
Ch. 24.1 - Prob. 1CCCh. 24.1 - Prob. 2CCCh. 24.1 - Prob. 3CCCh. 24.1 - Prob. 4CCCh. 24.1 - Prob. 5CCCh. 24.1 - Describe vesicular, ovular, and chromosomal...Ch. 24.1 - Why has taxonomic classification of protists been...Ch. 24.2 - Prob. 1MICh. 24.2 - What are the functions of the stigma and the...Ch. 24.2 - Prob. 1CC
Ch. 24.2 - What is the function of the plasmalemma and...Ch. 24.2 - Prob. 3CCCh. 24.3 - Prob. 1MICh. 24.3 - Prob. 2MICh. 24.3 - Prob. 1CCCh. 24.3 - Prob. 2CCCh. 24.3 - Prob. 3CCCh. 24.4 - Prob. 1MICh. 24.4 - What are the functions of the micronucleus and...Ch. 24.4 - How does the trigger for sexual reproduction...Ch. 24.4 - Prob. 1CCCh. 24.4 - Compare how radiolaria use axopodia with the way...Ch. 24.4 - Prob. 3CCCh. 24.4 - Prob. 4CCCh. 24.4 - Describe conjugation as it occurs in ciliates....Ch. 24.4 - Prob. 6CCCh. 24.4 - Prob. 7CCCh. 24.4 - Prob. 8CCCh. 24.4 - Prob. 9CCCh. 24.5 - Prob. 1MICh. 24.5 - Compare the morphology of members of the genus...Ch. 24.5 - Prob. 2CCCh. 24 - Prob. 1RCCh. 24 - Prob. 2RCCh. 24 - Prob. 3RCCh. 24 - Prob. 4RCCh. 24 - Prob. 5RCCh. 24 - Prob. 6RCCh. 24 - Protist encystment is usually triggered by changes...Ch. 24 - Vaccine development for diseases caused by...Ch. 24 - Prob. 3ALCh. 24 - Benthic foraminifera inhabit marine sediments. It...Ch. 24 - Prob. 5AL
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- Referring to the Standard Genetic Code table, categorize the chemical properties of each of the 24 amino acids that make up the ER Signal Peptide (hydrophobic, hydrophilic, positive charge, or negative charge). What is notable about the chemical properties of the amino acids that make up the ER Signal Peptide? methionine- translation code tra-hyperopic amino acid R Origine eukiauk aicd amino glutamine HYDOICO ACIDS gaac -CHANGED AMINO ACIDarrow_forward1) Given an mRNA with the following sequence, please translate the codons to a chain of amino acids. Use the codon chart below.5’AUG/CCU/GCU/UAC/CGG/GAG/UAA3’ “met-_________-_________-_________-_________-_________”STOP” 2) Assuming the original polypeptide chain below, match each type of point mutation with the polypeptide chain that results. Original polypeptide: Pro-Thr-Ser-Leu-Leu-His-Asn A. Missense B. Silent C. Nonsense D. Frameshift ______ Pro-Thr-Ser-STOP ______ Pro-Thr-Ser-Leu-Ile-His-Asn ______ Pro-Thr-Ser-Leu-Leu-His-Asn _______ Pro-Thr-His-Cys-Tyr-Thrarrow_forwarda) 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_forward
- a) 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_forwarda) 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_forward
- a) 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_forwardOverview of Transformation Protocol -Prepare competent bacteria for transformation: Treat starter E. coli bacteria with CaCl2and Competent Cell Solution (CCS). Store on ice until transformation procedure. Competent cells are cells that are likely to take up foreign DNA and be transformed. This step increases the likelihood that the E. coli cells will take up the introduced vector and be transformed. -Transformation procedure: Obtain two microcentrifuge tubes containing your competent cells. Label one tube +DNA and one -DNA. Add CaCl2 to both tubes. Add the transformation mix containing the plasmid DNA to the tube labeled +DNA. Do not add any plasmid DNA to the -DNA tube. Incubate both tubes on ice for 10 minutes. Then, place both tubes in a 42\deg C water bath for 45 seconds. Replace the tubes in an ice bucket for 2 minutes. Add recovery broth to both tubes. Incubate both tubes in a 37 C water bath for 5 minutes. Questions: 1) What differences would you expect to see between the…arrow_forward
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