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产黄青霉AS-P-78的pcbAB、pcbC和penDE基因的转录受葡萄糖抑制,且这种抑制不能通过碱性pH值逆转。

Transcription of the pcbAB, pcbC and penDE genes of Penicillium chrysogenum AS-P-78 is repressed by glucose and the repression is not reversed by alkaline pHs.

作者信息

Gutiérrez Santiago, Marcos Ana T, Casqueiro Javier, Kosalková Katarina, Fernández Francisco J, Velasco Javier, Martín Juan F

机构信息

Institute of Biotechnology, INBIOTEC, Parque Científico de León, Avda del Real 1, 24006 León, Spain.

Area of Microbiology, Faculty of Biology, University of León, 24071 León, Spain.

出版信息

Microbiology (Reading). 1999 Feb;145 ( Pt 2):317-324. doi: 10.1099/13500872-145-2-317.

Abstract

Glucose repressed transcription of the penicillin biosynthesis genes pcbAB, pcbC and penDE when added at inoculation time to cultures of Penicillium chrysogenum AS-P-78 but it had little repressive effect when added at 12 h and no effect when added at 24 or 36 h. A slight increase in the expression of pcbC and penDE (and to a smaller extent of pcbAB) was observed in glucose-grown cultures at pH 6.8, 7.4 and 8.0 as compared with pH 6.2, but alkaline pHs did not override the strong repression exerted by glucose. Transcription of the actin gene used as control was not significantly affected by glucose or alkaline pHs. Repression by glucose of the three penicillin biosynthetic genes was also observed using the lacZ reporter gene coupled to each of the three promoters in monocopy transformants with the constructions integrated at the pyrG locus. Glucose repression of the three genes encoding enzymes of penicillin biosynthesis therefore appears to be exerted by a regulatory mechanism independent from pH regulation.

摘要

在接种时向产黄青霉AS-P-78培养物中添加葡萄糖会抑制青霉素生物合成基因pcbAB、pcbC和penDE的转录,但在12小时添加时抑制作用很小,在24或36小时添加时则无作用。与pH 6.2相比,在pH 6.8、7.4和8.0的葡萄糖培养物中观察到pcbC和penDE(以及程度较小的pcbAB)的表达略有增加,但碱性pH并未克服葡萄糖所施加的强烈抑制作用。用作对照的肌动蛋白基因的转录不受葡萄糖或碱性pH的显著影响。在单拷贝转化体中,使用与三个启动子中的每一个偶联的lacZ报告基因,并将构建体整合到pyrG位点,也观察到葡萄糖对三个青霉素生物合成基因的抑制作用。因此,葡萄糖对编码青霉素生物合成酶的三个基因的抑制作用似乎是由一种独立于pH调节的调控机制施加的。

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