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吸水链霉菌中双丙氨膦生物合成的转录调控

Transcriptional regulation of bialaphos biosynthesis in Streptomyces hygroscopicus.

作者信息

Anzai H, Murakami T, Imai S, Satoh A, Nagaoka K, Thompson C J

出版信息

J Bacteriol. 1987 Aug;169(8):3482-8. doi: 10.1128/jb.169.8.3482-3488.1987.

Abstract

A DNA sequence (brpA) which regulates the expression of the genes of the bialaphos biosynthesis pathway (bap) in Streptomyces hygroscopicus was identified and characterized. A newly isolated nonproducing mutant (NP57) had a pleiotropic defect involving at least 6 of the 13 known bap genes; only the step 6 conversion could be detected. NP57 was more sensitive to bialaphos than its parent and had depressed levels of the demethylphosphinothricin acetyltransferase activity (step 10 in the pathway) which confers bialaphos resistance. Sodium dodecyl sulfate-polyacrylamide gel electrophoretic analysis of extracts of this mutant showed that it lacked proteins corresponding to steps 5 and 10. NP57 lacked mRNAs for steps 5, 10, and 13. Bialaphos productivity of NP57 was restored by transformation with a plasmid containing a 5.9-kilobase DNA fragment which was adjacent to the structural gene cluster. Subcloning experiments showed that a 1.3-kilobase fragment from this primary clone restored all the defects of NP57. We conclude that brpA can activate the transcription of the bialaphos resistance gene as well as at least six other bap structural genes.

摘要

鉴定并表征了一种调节吸水链霉菌中双丙氨膦生物合成途径(bap)基因表达的DNA序列(brpA)。新分离出的不产生双丙氨膦的突变体(NP57)存在多效性缺陷,涉及13个已知bap基因中的至少6个;仅能检测到第6步转化。NP57对双丙氨膦比其亲本更敏感,且赋予双丙氨膦抗性的去甲基膦丝菌素乙酰转移酶活性(该途径中的第10步)水平降低。对该突变体提取物进行的十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析表明,它缺乏与第5步和第10步相对应的蛋白质。NP57缺乏第5、10和13步的mRNA。通过用含有与结构基因簇相邻的5.9千碱基DNA片段的质粒转化,恢复了NP57的双丙氨膦生产能力。亚克隆实验表明,来自该原始克隆的1.3千碱基片段恢复了NP57的所有缺陷。我们得出结论,brpA可以激活双丙氨膦抗性基因以及至少其他六个bap结构基因的转录。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d97/212421/c4bc9a0d8959/jbacter00198-0101-a.jpg

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