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- Define/Compare/Contrast/Distinguish these three terms: F plasmid F’ plasmid (and how is it formed) Hfr cell (and how is it formed)dont copy from chegg or other source please give me detail answerSecond letter A G UCU UCC UAU. Tyr UAC. UUU1 Phe UUC. UUA UUG. UGC Ser }Leu UAA Stop UGA Stop UAG Stop |UGG Trp UCA UCG CAU His CUU CỤC CCU ССС ССА CGU CGC Arg Leu CÁCS Pro CỦA CUG CGA CAAGIN CGG, Gln CAG, CCG J AAU Asn ACU АСC АСА AUU AGU Ser AUC }le A AUA AAC. Thr А AGC AGA AUG Met | ACG ] AAG Lys AG. GUU GUC GCU GAU1 AAsp GACS Ala GAA GGU GGC GCC Val Gly GGA G GUA GCA GUG GCGJ GAG Glu GGG Which peptide is the least likely to be made on the ribosome and why? а. Third letter DUAG 5UAG DUAG DUAG First letter
- Please answer with yes or no with correcting the falte statement. Felline to cottart the will cost the whole statements mark, 56) Prionsare small circular RNA Viruses, those viruses don't have capsid and they can't replicate in their own. They need & helper virus like hepatitis If virus to replicate 57) Car receptor can act as a receptor for multiple viruses, like adenoviruses and Herpesviruses. 58) For infiuenza viruses they enter the host cell via Clathrien-coated pits endocytosis; in which the cell receptors will be digested by the lysozyme enzymes 59) Uncosting is the removal of the outer capsid in order to release the genome to start the viral replication, In case of adenovirus the uncoalo appen.. membraneIdentify a plasmid that is used to destroy its competitors. fertility plasmids bacteriocin plasmids virulence plasmids cryptic plasmids resistance plasmids2 3 inte tion of Lormhda. ne att si ucated betwee de ne att sites and go ns one te n vacter aged ot utilize doot ractose ato la t don s gal* uc Integration to form prophage om SOward cor coct some cro on! ni imple ex 2 3 bio* gal* 14. The figure provided portrays the integration of Lambda phage into a host chromosome at the att site, located between the gal+ and bio+ genes. This prophage may disintegrate from the host carrying with it host genes, such as gal+ and/or bio+ and go on to transduce another host bacterium. How would one determine if a gal- host bacterium's phenotype was changed from gal- to gal+? To clarify, the minus version cannot utilize galactose as a carbon source for growth because it does not produce galactase, the enzyme that hydrolyzes galactose into monomeric sugars. There is a straight forward answer/solution to this – do not concoct some crazy solution! Think simple experiment.