A series of auxotrophic mutants were isolated in Neurospora. Examination of fungi containing these mutations revealed that they grew on minimal medium to which various compounds (A, B, C, D) were added; growth responses to each of the four compounds are presented in the following table. Give the order of compounds A, B, C, and D in a biochemical pathway. Outline a biochemical pathway that includes these four compounds and indicate which step in the pathway is affected by each of the mutations. Compound Mutation number А в С A D 134 276 987 773 772 146 333 123 + + I +
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- A number of auxotrophic mutant strains were isolated from wild-type haploid Neurospora crassa. These strains responded to the addition of certain nutritional supplements to minimal culture medium either by growth (+) or no growth (0) The data from this experiment are presented in the table below. Diagram a biochemical pathway, complete with positions of intermediates, that is consistent with the data. Indicate where in the pathway each mutant strain is blocked.A classic way to isolate thymidylate synthase–negative mutants of bacteriais to treat a growing culture with thymidine and trimethoprim. Most ofthe cells are killed, and the survivors are greatly enriched in thymidylatesynthase–negative mutants.(a) What phenotype would allow you to identify these mutants?(b) What is the biochemical rationale for the selection? (That is, why are themutants not killed under these conditions?)(c) How would the procedure need to be modified to select mammalian cellmutants defective in thymidylate synthase?. Mutants of Neurospora crassa that lack carbamoyl phosphate syn- thetase I (CPS I) require arginine in the medium in order to grow, whereas mutants that lack carbamoyl-phosphate synthetase II (CPS II) require a pyrimidine, such as uracil. A priori, one would expect the active CPS II in the arginine mutants to provide sufficient carbamoyl phosphate for arginine synthesis, and the active CPS I in the pyrimidine mutants to "feed" the pyrimidine pathway. Explain these observations.
- The pathway for cystiene synthesis in E.coli involves five precursor compounds, compound A-E. The requirements for each of the autotrophs are summarized in the table below. Use the data, define the biosynthetic pathway. Draw the pathway for cysteine synthesis. Fill in the blanks with A-E compounds as appropriate and then label the arrows with the auxotrophs C1-C8 that are unable to complete that step. There are may be more than one quxotroph that is defective at a particular step. that is - on C4 in DConsider the biochemical pathway shown here. Suppose that a strain of bacteria must synthesize compound 4 to survive and divide. Successful survival and division of bacteria is observed as growth of colonies on an agar plate. This strain of bacteria can grow colonies on minimal medium as long as it is supplemented with compound 1. You are in a lab that has isolated several mutants of this strain. You find that these mutants cannot grow on minimal medium supplemented with compound 1, though they can grow colonies if supplemented with compound 4. Considering what you know about the Beadle-Tatum experiments, which of the following statements would be one that should be true?Under cellular conditions, dATP can be oxidized to its 2-hydroxy form, which is a substrate for an enzyme that converts 2-OH-dATP to 2-OH-dAMP + PPi. Explain why compounds that inhibit the activity of this enzyme would be eff ective anticancer agents.
- A conjugate was incubated with a mixture of lysosomal enzymes and no drug release was observed in these conditions. The same conjugate was tested for antitumor activity in vivo and an anticancer effect was observed. Taking into account the information provided above, hypothesize a possible mechanism of action for this conjugate.The intermediates A, B, C, D, E, and F all occur inthe same biochemical pathway. G is the product of thepathway, and mutants 1 through 7 are all G−, meaningthat they cannot produce substance G. The followingtable shows which intermediates will promote growthin each of the mutants. Arrange the intermediates inorder of their occurrence in the pathway, and indicatethe step in the pathway at which each mutant strain isblocked. A + in the table indicates that the strain willgrow if given that substance, an O means lack of growth.SupplementsMutant A B C D E F G1 + + + + + O +2 O O O O O O +3 O + + O + O +4 O + O O + O +5 + + + O + O +6 + + + + + + +7 O O O O + O +Sydney Brennen isolated Salmonella typhimurium mutants that were implicated in the biosynthesis of tryptophan and would not grow on minimal medium supplemented with intermediates in tryptophan biosynthesis, some mutants were able to grow while others remained unable to grow. Review the data attached to order the biosynthetic pathway by both enzymatic step and by intermediate biomolecule. Label the step impacted by each of the mutant cell lines.
- You are studying a biochemical pathway and isolate Neurospora mutants I, II, and III.Mutant I can grow if you supplement the medium with Z.Mutant II can grow if you supplement the medium with X, Y, or Z.Mutant III can grow if you supplement the medium with X and Z, but not with Y. Draw a biochemical pathway that shows the correct order for compounds X, Y, and Z and for the enzymes that each mutant is defective for.Various antimicrobial drugs to treat microbial infection have diverse mechanism of action. Consider the following antimicrobial drugs: A. Seconeolitsine, known as DNA topoisomerase I inhibitor in bacteria. (i) Explain briefly how inhibiting DNA topoisomerase I is a good mechanism of action for an antibiotic, include possible molecular machineries being targeted. (ii) What would be an appropriate response if seconeolitsine works well by stating the state of supercoiling in bacteria. (iii) To prove your answer (ii), you test the condition of bacterial DNA by running gel electrophoresis, one has been treated with seconeolitsine (+ sample) and the other one is not (- sample). Explain the position of each + sample and – sample band on the gel in reference to the point of origin (where you load your samples) or how far each DNA sample travel across agarose gel. (iv) Explain why you would expect answer (iii) for each + sample and – sample. B.…The macrolide below is a bacteria produced toxin. The primer was acetyl-Co-A. Three possible extenders are also shown A) malonate-Co-A B) methylmalonate-Co-A and C) ethylmalonate-Co-A. Indicate which extenders were used using this format: XA yB zC Meaning x molecules of A, y molecules of B and z molecules of C A COA но CH3 но, CH3 COA H3C CH3 B но HO CH3 CH3 HO CH3 C COA но CH3 Enter Your Answer: