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A-因子对链霉菌形态发育和次级代谢的激素控制。

Hormonal control by A-factor of morphological development and secondary metabolism in Streptomyces.

机构信息

Department of Biotechnology, Graduate School of Agriculture and Life Sciences, The University of Tokyo, Tokyo, Japan .

Advanced Research Institute for the Science and Humanities, Nihon University, Tokyo, Japan .

出版信息

Proc Jpn Acad Ser B Phys Biol Sci. 2007 Dec;83(9-10):277-95. doi: 10.2183/pjab/83.277.

Abstract

Streptomyces griseus, a well-known industrial producer of streptomycin, is a member of the genus Streptomyces, which shows a complex life cycle resembling that of fungi. A-factor, a C13 γ-butyrolactone compound, was discovered as a self-regulatory factor or a bacterial hormone to induce morphological differentiation and production of secondary metabolites, including streptomycin, in this organism. Accumulating evidence has revealed an A-factor-triggered signal cascade, which is composed of several key steps or components. These include: (i) AfsA catalyzing a crucial step of A-factor biosynthesis, (ii) the A-factor-specific receptor (ArpA), which acts as a transcriptional repressor for adpA, (iii) adpA, a sole target of ArpA, which encodes a global transcriptional activator AdpA, and (iv) a variety of members of the AdpA regulon, a set of the genes regulated by AdpA. A-factor is biosynthesized via five reaction steps, in which AfsA catalyzes acyl transfer between a β-ketoacyl-acyl carrier protein and the hydroxyl group of dihydroxyacetone phosphate. The receptor ArpA, belonging to the TetR family, is a homodimer, each subunit of which contains a helix-turn-helix DNA-binding motif and an A-factor-binding pocket. The three-dimensional structure and conformational change upon binding A-factor are elucidated, on the basis of X-ray crystallography of CprB, an ArpA homologue. AdpA, belonging to the AraC/XylS transcriptional activator family, binds operators upstream from the promoters of a variety of the target genes and activates their transcription, thus forming the AdpA regulon. Members of the AdpA regulon includes the pathway-specific transcriptional activator gene strR that activates the whole streptomycin biosynthesis gene cluster, in addition to a number of genes that direct the multiple cellular functions required for cellular differentiation in a concerted manner. A variety of A-factor homologues as well as homologues of afsA/arpA are distributed widely among Streptomyces, indicating the significant role of this type of molecular signaling in the ecosystem and evolutional processes.

摘要

灰色链霉菌是链霉菌属的一种,是链霉素的工业生产菌,具有复杂的生命周期,类似于真菌。A-因子是一种 C13γ-丁内酯化合物,作为一种自我调节因子或细菌激素,被发现可以诱导该生物的形态分化和次生代谢产物的产生,包括链霉素。越来越多的证据揭示了一个由 A-因子触发的信号级联,该级联由几个关键步骤或组成部分组成。这些包括:(i)AfsA 催化 A-因子生物合成的关键步骤,(ii)A-因子特异性受体(ArpA),它作为 adpA 的转录阻遏物,(iii)adpA,是 ArpA 的唯一靶标,编码全局转录激活物 AdpA,以及(iv)AdpA 调控子的各种成员,即一组由 AdpA 调节的基因。A-因子通过五个反应步骤生物合成,其中 AfsA 催化β-酮酰-酰基辅酶 A 与二羟丙酮磷酸的羟基之间的酰基转移。受体 ArpA 属于 TetR 家族,是一个同源二聚体,每个亚基包含一个螺旋-转角-螺旋 DNA 结合基序和一个 A-因子结合口袋。根据 CprB(ArpA 的同源物)的 X 射线晶体结构,阐明了结合 A-因子时的三维结构和构象变化。AdpA 属于 AraC/XylS 转录激活因子家族,结合各种靶基因启动子上游的操纵子并激活它们的转录,从而形成 AdpA 调控子。AdpA 调控子的成员包括途径特异性转录激活基因 strR,它激活整个链霉素生物合成基因簇,以及许多基因,这些基因以协同的方式指导细胞分化所需的多种细胞功能。A-因子的各种类似物以及 afsA/arpA 的类似物广泛分布在链霉菌中,表明这种类型的分子信号在生态系统和进化过程中具有重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f56d/3859367/cc4f28a6218f/83_277f1.jpg

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