Titlebook: Gene Manipulation and Expression; Robert E. Glass,Jaroslav Spi?ek Book 1985 Robert E. Glass and Jaroslav Spi?ek 1985 DNA.Elongation.Promot

Resign

種子

Genomic Structure and Evolution of , ? and LP52 Phage Familyf not identical prophage was found in . ATCC 11946 and was called LP51. The second prophage called DLP 10716 (Fig.l.1C) is inducible with mitomycin C and produces particles with small isodiametric heads and tails with contractile sheaths; these particles do not form plaques because they contain random cuts of host DNA.

Missile

Host Vector System with the PR, Promoter of Phage Lambda late genes results from antitermination of the 6S RNA, a transcript permanently synthesized from the P.. promoter (1). Therefore in order to create a host-vector system with the P., promoter it is necessary that the defective pro-phage includes the genes .I, . and ., and has a deletion of the late genes.

小卷發(fā)

Genomic Structure and Evolution of , ? and LP52 Phage Familyidentified as the agent responsible for lysis of an industrial batch of . in a bacitracin-producing factory. The lytic form of phage ? was described by Ludvík .. (1), who called it the BLE phage; we found, however, that it may occur in various lytic as well as temperate forms and denominated the who

Contracture

Expression of the Synthetic Proenkephalin Gene in ,nd intestine (1). Based on the study of enkephalin-containing peptides, it was postulated that enkephalins are released from a larger precursor protein (2). The primary structure of this proenkephalin was later derived from the cloned DNA complementary to the proenkephalin mRNA (3–6). The precursor

Gourmet

Cloning and Expression of ,,-Glucanase Genesrange of these bacterial .-glucan-endohydrolases is similar to that of lichenase (EC 3.2.1.73, 1,3;1,4-.-glucan 4-glucano-hydrolase) of germinating barley and restricted to mixed linked glucans such as lichenan and barley .-glucan (2). Cellobiosyl-D-glucose and cellotriosyl-D-glucose are the main pr

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