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氨基酸对构巢曲霉青霉素生物合成基因acvA(pcbAB)的调控:转录因子PACC参与的意义。

Regulation of the Aspergillus nidulans penicillin biosynthesis gene acvA (pcbAB) by amino acids: implication for involvement of transcription factor PACC.

作者信息

Then Bergh K, Brakhage A A

机构信息

Lehrstuhl für Mikrobiologie, Universität München, Federal Republic of Germany.

出版信息

Appl Environ Microbiol. 1998 Mar;64(3):843-9. doi: 10.1128/AEM.64.3.843-849.1998.

Abstract

The beta-lactam antibiotic penicillin is produced as an end product by some filamentous fungi only. It is synthesized from the amino acid precursors L-alpha-aminoadipic acid, L-cysteine, and L-valine. Previous data suggested that certain amino acids play a role in the regulation of its biosynthesis. Therefore, in this study the effects of externally added amino acids on both Aspergillus (Emericella) nidulans penicillin production and expression of the bidirectionally oriented biosynthesis genes acvA (pcbAB) and ipnA (pcbC) were comprehensively investigated. Different effects caused by amino acids on the expression of penicillin biosynthesis genes and penicillin production were observed. Amino acids with a major negative effect on the expression of acvA-uidA and ipnA-lacZ gene fusions, i.e., histidine, valine, lysine, and methionine, led to a decreased ambient pH during cultivation of the fungus. An analysis of deletion clones lacking binding sites for the pH-dependent transcriptional factor PACC in the intergenic regions between acvA-uidA and ipnA-lacZ gene fusions and in a pacC5 mutant (PacC5-5) suggested that the negative effects of histidine and valine on acvA-uidA expression were due to reduced activation by PACC under acidic conditions. These data also implied that PACC regulates the expression of acvA, predominantly through PACC binding site ipnA3. The repressing effect caused by lysine and methionine on acvA expression, however, was even enhanced in one of the deletion clones and the pacC5 mutant strain, suggesting that regulators other than PACC are also involved.

摘要

β-内酰胺抗生素青霉素仅由一些丝状真菌作为终产物产生。它由氨基酸前体L-α-氨基己二酸、L-半胱氨酸和L-缬氨酸合成。先前的数据表明某些氨基酸在其生物合成调控中起作用。因此,在本研究中,全面研究了外源添加氨基酸对构巢曲霉(Emericella)青霉素产生以及双向定向生物合成基因acvA(pcbAB)和ipnA(pcbC)表达的影响。观察到氨基酸对青霉素生物合成基因表达和青霉素产生有不同的影响。对acvA-uidA和ipnA-lacZ基因融合表达有主要负面影响的氨基酸,即组氨酸、缬氨酸、赖氨酸和蛋氨酸,导致真菌培养过程中环境pH值降低。对在acvA-uidA和ipnA-lacZ基因融合之间的基因间区域以及pacC5突变体(PacC5-5)中缺乏pH依赖性转录因子PACC结合位点的缺失克隆进行分析表明,组氨酸和缬氨酸对acvA-uidA表达的负面影响是由于酸性条件下PACC的激活减少。这些数据还暗示PACC主要通过PACC结合位点ipnA3调节acvA的表达。然而,赖氨酸和蛋氨酸对acvA表达的抑制作用在其中一个缺失克隆和pacC5突变体菌株中甚至增强,这表明除PACC外的其他调节因子也参与其中。

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