Construct a dichotomous key (design or presentation of your own choice; example is the diagram below) using the data of the bacteria in the list.
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Q: of.
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Construct a dichotomous key (design or presentation of your own choice; example is the diagram below) using the data of the bacteria in the list.
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- Enzyme Carboxypeptidase A CBZ-NH-CH, C-NH-CH-COOH CH₂ C6H5 Papain a-chymotrypsin Substrate HIV protease N-CBZ-glycyl-L-phenylalanine ก CBZ-NHCH--C--NH-CH, CẢNH CH2 CH₂ N-CBZ-L-phenylalanyl-glycyl- p-nitroanilide CHỦ NHCH I CH2 CH --NH-CH-C-NH--CH,-COOH N-acetyl-L-phenylalanyl-glycine NH on C.NH NO₂ CH3 CH₂ CH2 C6H5 -NH-CH--COOH 1 CH3 N-acetyl-L-valyl-L-phenylalanyl-L-alanine Inhibitor I i CBZ-NH-CH -C--NH-CH-COOH 3Z--NH-CH I CH 3 CH2 C Hs N-CBZ-D-alanyl-L-phenylalanine CBZ--NH-CH--C--NH--CH, I CH₂ C6H5 N-CBZ-L-phenylalanyl-glycinal CH3-C-NH-CH-C-OH CH₂ C6H5 N-acetyl-L-phenylalanine CH3 quemq CH₂-CH-COOH -NH-CH-C-CH2-CH-COOH CH2 CH3 CH3 CH3 C6H5 --NH-- N-(N-(acetyl)-valyl)-5-amino-5-benzyl-4-keto- 2-methyl-pentanoic acid Inhibitor II CBZ-NH-CH₂--P--NH--CH--COOH 0 N-(CBZ-aminomethyl-oxyhydroxyphos- phinyl)-L-phenylalanine 1 CH2 C6H5 CBZ--NH-CH--C--NH-CH2-COOH I CH 2 C6H5 i N-CBZ-L-phenylalanyl-glycine CH3--C--NH--CH--CH(OH)CH₂CH2COOH CH2 C6H5 N-acetyl-5-amino-5-benzyl-4-hydroxy-…What is the name of the fungal toxin that inhibits RNA polymerase Il at 1 microgram/mL concentration? O Flavopiridol a-Amanitin O Triptolide DRB (5,6-Dichloro-1-ß-D- ribofuranosylbenzimidazole)3. The table on the last page compares for each of four different proteolytic enzymes the chemical bonding structure of a classical substrate with the structures of two competitive inhibitors. For each substrate structure an arrow indicates the position of the scissile bond, i.e., the bond that is cleaved through catalytic action. For each enzyme, one of the inhibitors is a classical competitive inhibitor while the other is a transition-state inhibitor analog. While ordinary competitive inhibitors are associated with (dissociation) inhibitor equilibrium con- stants of ~10-3 to 10-6 M, transition-state analogs exhibit inhibitor constants ≤ 10-⁹ M. (a) For each enzyme draw a circle around those parts of the substrate that account for specificity of substrate recognition. (b) For each enzyme identify the transition-state inhibitor analog by drawing a circle around it and give a brief explanation of why it mimics the structure of the transition-state species. (c) Draw a "generic"…
- 10-Corynebacterium diphtheria related to: A-g+ve cocci B-g-ve cocci C-g-ve rods D-g+ve rodsplease sir please solve this matching question, thank you alot for ur helpSome antibiotics target peptidoglycan synthesis. What is amolecular growth target of an antibiotic that inhibitspeptidoglycan synthesis?
- OalgaeBASE dpalgaeBAsE B galgaeBASE Figure 3. A. Oscillatoria and B. Anabaena under microscope Reference source: https://www.algaebase.org/search/pictures/ 1. What is the colony morphology of these two cyanobacterial species having?Corynebacterium xerosis ~1X 2 micron Notice: angular and palisades 中e-Please complete the table on basis of the categories mentioned.
- Describe the bacteria staphylococci based on the table attachedIchthyophthirius multifiliis - the etiologic agent of "ich". Life Cycle What role do each of the following play? Organelle of Lieberkunn perforatorium mucocystb. Cleavage with chymotrypsin produces the following fragments: Band A: CN , NLQY, GIVEQCCHKRSEY Band B: F, Y, DPTKM, IACCVRGF, RTTGHLCGKDLVNALY Cleavage with Staphilococcus aureus V8 protease produces the following fragments: Band A: GIVE, YNLQNYCN, QCCHKRCSE Band B: PTKM, RTTGHLCGKD, LVNALYIACGVRGFFYD What is the amino acid sequence of the protein? Type your response