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首页> 外文期刊>Journal of bacteriology >Functional analysis of putative beta-ketoacyl:acyl carrier protein synthase and acyltransferase active site motifs in a type II polyketide synthase of Streptomyces glaucescens.
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Functional analysis of putative beta-ketoacyl:acyl carrier protein synthase and acyltransferase active site motifs in a type II polyketide synthase of Streptomyces glaucescens.

机译:褐链霉菌的II型聚酮化合物合酶中推定的β-酮酰基:酰基载体蛋白合酶和酰基转移酶活性位点基序的功能分析。

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摘要

The significance of potential active site motifs for acyltransferase and beta-ketoacyl:acyl carrier protein synthase regions within the TcmK protein was investigated by determining the effects of mutations in the proposed active sites on the production of tetracenomycins F2 and C. In a Streptomyces glaucescens tcmGHI JKLMNO null mutant, plasmids carrying the S351A mutation produced high amounts of tetracenomycin F2 but plasmids carrying the C173A or C173S mutation or the H350L-S351A double mutation produced no detectable amount of any known intermediate. In a tcmK mutant, plasmids with the S351A mutation restored high production of tetracenomycin C and plasmids carrying the other mutations were able to complement the chromosomal defect to some extent. None of the mutations affected the amount of TcmK produced.
机译:通过确定拟议的活性位点中的突变对丁菌霉素F2和C产生的影响,研究了TcmK蛋白中酰基转移酶和β-酮酰基:酰基载体蛋白合酶区域的潜在活性位点基序的重要性。 JKLMNO无效突变体,带有S351A突变的质粒产生了大量的土霉素霉素F2,但是带有C173A或C173S突变或H350L-S351A双重突变的质粒则未产生可检测量的任何已知中间体。在tcmK突变体中,具有S351A突变的质粒可恢复丁菌霉素C的高产量,而带有其他突变的质粒则可以在一定程度上弥补染色体缺陷。这些突变均不影响产生的TcmK的量。

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