4. After incubation of the mating mixture for 1 hour, prepare a serialdilution of the mating mixture in sterile saline (to 103). As described instep 2, clearly label each of the double selective agar plates (i.e. (i)Nutrient agar+ Ap + Rif, (ii) Nutrient agar+ Sm + Rif) AND iii) theNutrient agar + Ap + Sm + Rif plate. Spot inoculate 3 x 10 µl drops ofthe undiluted, 10-1, 10-2 and 10-3 dilutions of the mating mix ontoquadrants of each of these plates.• What is the purpose of this step?

The purpose of this step is to distinctly identify and count the number of colonies in the double…

Answered: After incubation of the mating mixture…

Biochemistry

9th Edition

ISBN:9781319114671

Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.

Publisher:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.

Chapter1: Biochemistry: An Evolving Science

Section: Chapter Questions

Problem 1P

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Answer the following questions briefly and concisely 1.How do bacteria in a chemostat and those in a batch culture vary from one another? 2. What happens in a chemostat if the dilution rate is higher than the organism's maximum specific growth rate? 3.Does a chemostat require the use of pure cultures? 4. Why would a complicated culture media for Leuconostoc mesenteroides be simpler to make than one with a fixed chemical composition?
Consider the desired phenotype pattern of candidates that we wish to advance into experiments in Week 5 and beyond. If the growth patterns illustrated below are observed in your Week 4 results, which of the candidates would you select for further analysis? Select all that apply. Candidate A B A B C с = vigorous growth on this medium = impaired/slow growth on this medium = no growth on this medium SC-H B SC-K A B YP Gal
You have several different media onto which you inoculated eight strains of yeast (A-H). The media include a rich medium, an unsupplemented minimal medium, and minimal media each supplemented with one vitamin. Of the yeast strains, one is a prototroph and seven are auxotrophs for a vitamin. After overnight incubation, the following results were observed (tan patches represent growth): D plate 1 (A) B DE F GH plate 5 plate 4 plate 6 Which plate contains an unsupplemented minimal medium? [Select] Which plate contains a rich medium? [Select] plate 2 Which strain is a prototroph? [Select] Strain E is an auxotroph for niacin. Which plate reveals this specific auxotrophy? [ Select] plate 3 plate 7 One strain is an auxotroph for both choline and pantothenic acid. Which one is this most likely to be? [Select]
explain the various factors affecting agar-agar gels and what is the source, manufacturing, and properties of agar-agar and what is the uses of agar-agar in food products?
Using the attached image, explain the observed results on the NA and ECM plates. Be sure to address why each sample is either able or unable to grow on each plate and include the genotype(s) of the cells which are capable of growth.
Two dyes wereplaced in an agar gel. Which dye migrated through thegel faster? Why? Explain in brief simply terms
A culture consisting of 100 litres of nutrient medium containing 12 g l-1 of growth limiting substrate is inoculated with 10g of bacteria in a batch fermenter. The yield of biomass from substrate is 0.05 g g-1 . The maintenance coefficient is 2.0 g g-1 h -1 . The specific rate of product formation due to maintenance is 1.0 h-1 . The maximum specific growth rate of the organism is 0.3 h -1 . YPX= 7.7 and product formation is directly linked with metabolism. a) What is the time required to produce 15 g of biomass? !!!!! ANS IS 3.07 HRS!!!! STEPS on how to reach this please
A phagehunter performs a spot titer using standard techniques (3 ul of each dilution spotted to lawn) of a lysate obtained from an optimum webbed plate experiment. The phagehunter counts 4 plaques on the 10-8 dilution spot. Which of the following scenarios is the best choice for the phagehunter to do next? a.) The phagehunter has not achieved a high enough titer lysate to move forward with characterization experiments, so they should try to make more optimum webbed plates. b.) The phagehunter has not achieved a high enough titer lysate to move forward with characterization experiments, so they should adopt a phage from direct isolation. c.) The phagehunter has achieved a high enough titer lysate to move forward with characterization experiments. d.) The phagehunter has not achieved a high enough titer lysate to move forward with characterization experiments, so they should go back to the pick-a-plaque experiment.
If an organism that showed no growth in the MIC broth test at a particular dose, then grows in an MBC test when plated to media, the concentration of the drug was bacteriostatic. O 1) True O 2) False
50 g of food is homogenized in 450 mL of water. From this, 1 mL is added to 29 mL of water, and then a 1:90 dilution is made from this, and then 1 mL from this is added to 99 mL of water, and then 100 uL of this last dilution is plated and after incubation 164 colonies are counted.a) What was the overall dilution factor?b) What was the total CFU/g of the original sample?
Draw a semi-logarithmic diagram showing the killing kinetics of a vegetative bacterial culture, assuming appropriate temperature, e.g. 100°C. Label the axes. 1.) What are the kinetics for killing bacterial spores at 100°C and 121°C 2.) and what about a mixture of different heat-resistant vegetative cells?
Suppose that you were tasked with 4 cultures of a specific Bacteria Species in Luria Broth medium: (1) culture A – cells are in lag phase; (2) culture B – cell in log phase; (3) culture C – cells in stationary phase; and culture D – cells in decline phase. Imagine that you observe the growth rates of each culture in a fresh sterilized LB medium. Now, plot the outcome growth curves of cultures A, B, C and D in a single graph.

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