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CefR 调节β-内酰胺中间体的转运蛋白,防止青霉素向发酵液中流失,并提高顶头孢霉中的头孢菌素产量。

CefR modulates transporters of beta-lactam intermediates preventing the loss of penicillins to the broth and increases cephalosporin production in Acremonium chrysogenum.

机构信息

Institute of Biotechnology, Av. Real s/n, León, Spain.

出版信息

Metab Eng. 2011 Sep;13(5):532-43. doi: 10.1016/j.ymben.2011.06.004. Epub 2011 Jun 21.

Abstract

The Acremonium chrysogenum cephalosporin biosynthetic genes are divided in two different clusters. The central step of the biosynthetic pathway (epimerization of isopenicillin N to penicillin N) occurs in peroxisomes. We found in the "early" cephalosporin cluster a new ORF encoding a regulatory protein (CefR), containing a nuclear targeting signal and a "Fungal_trans" domain. Targeted inactivation of cefR delays expression of the cefEF gene, increases penicillin N secretion and decreases cephalosporin production. Overexpression of the cefR gene decreased (up to 60%) penicillin N secretion, saving precursors and resulting in increased cephalosporin C production. Northern blot analysis revealed that the CefR protein acts as a repressor of the exporter cefT and exerts a small stimulatory effect over the expression level of cefEF that explains the increased cephalosporin yields observed in transformants overexpressing cefR. In summary, we describe for the first time a modulator of beta-lactam intermediate transporters in A. chrysogenum.

摘要

顶头孢霉头孢菌素生物合成基因位于两个不同的簇中。生物合成途径的中心步骤(异青霉素 N 到青霉素 N 的差向异构化)发生在过氧化物酶体中。我们在“早期”头孢菌素簇中发现了一个新的 ORF,它编码一个调节蛋白(CefR),含有一个核靶向信号和一个“真菌转移”结构域。CefR 的靶向失活延迟了 cefEF 基因的表达,增加了青霉素 N 的分泌,降低了头孢菌素的产量。CefR 基因的过表达降低了(高达 60%)青霉素 N 的分泌,节省了前体,导致头孢菌素 C 的产量增加。Northern blot 分析表明,CefR 蛋白作为出口蛋白 cefT 的抑制剂,对 cefEF 的表达水平有轻微的刺激作用,这解释了在过表达 cefR 的转化体中观察到的头孢菌素产量增加。总之,我们首次描述了顶头孢霉中β-内酰胺中间体转运蛋白的调节剂。

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