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薰衣草链霉菌FRI-5的γ-丁内酯信号系统中靛蓝生物合成基因lbpA的鉴定与表征

Identification and characterization of lbpA, an indigoidine biosynthetic gene in the γ-butyrolactone signaling system of Streptomyces lavendulae FRI-5.

作者信息

Pait Ivy Grace Umadhay, Kitani Shigeru, Kurniawan Yohanes Novi, Asa Maeda, Iwai Takashi, Ikeda Haruo, Nihira Takuya

机构信息

International Center for Biotechnology, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871, Japan.

Kitasato Institute for Life Sciences, Kitasato University, 1-15-1 Kitasato, Sagamihara, Kanagawa 252-0373, Japan.

出版信息

J Biosci Bioeng. 2017 Oct;124(4):369-375. doi: 10.1016/j.jbiosc.2017.04.020. Epub 2017 May 20.

Abstract

Streptomyces lavendulae FRI-5 produces the blue pigment indigoidine and other secondary metabolites (d-cycloserine and nucleoside antibiotics). The production of these useful compounds is controlled by a signaling cascade mediated by the γ-butyrolactone autoregulator IM-2. Previously we revealed that the far regulatory island includes the IM-2 receptor, the IM-2 biosynthetic enzyme, and several transcriptional regulators, and that it contributes to the regulation of indigoidine production in response to the signaling molecule. Here, we found that the vicinity of the far regulatory island includes the putative gene cluster for the biosynthesis of indigoidine and unidentified compounds, and demonstrated that the expression of the gene cluster is under the control of the IM-2 regulatory system. Heterologous expression of lbpA, encoding a plausible nonribosomal peptide synthetase, in the versatile model host Streptomyces avermitilis SUKA22 led to indigoidine production, which was enhanced dramatically by feeding of the indigoidine precursor l-glutamine. These results confirmed that LbpA is an indigoidine biosynthetic enzyme in the IM-2 signaling cascade.

摘要

薰衣草链霉菌FRI-5可产生蓝色色素靛玉红及其他次级代谢产物(d-环丝氨酸和核苷类抗生素)。这些有用化合物的产生受γ-丁内酯自调控因子IM-2介导的信号级联控制。此前我们发现,远端调控岛包含IM-2受体、IM-2生物合成酶和几个转录调控因子,且其有助于响应信号分子对靛玉红产生的调控。在此,我们发现远端调控岛附近包含靛玉红及未知化合物生物合成的假定基因簇,并证明该基因簇的表达受IM-2调控系统控制。在通用模式宿主阿维链霉菌SUKA22中对编码一种可能的非核糖体肽合成酶的lbpA进行异源表达,可导致靛玉红的产生,通过添加靛玉红前体L-谷氨酰胺可显著增强该产量。这些结果证实LbpA是IM-2信号级联中的一种靛玉红生物合成酶。

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