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SCO7832的功能表达通过链霉菌CK4412中途径特异性调控基因的过表达刺激了互隔交链孢酚单甲醚的产生。

Functional expression of SCO7832 stimulates tautomycetin production via pathway-specific regulatory gene overexpression in Streptomyces sp. CK4412.

作者信息

Park Shin-Hae, Choi Si-Sun, Kim Yoon Jung, Chang Yong Keun, Sherman David H, Kim Eung-Soo

机构信息

Department of Biological Engineering, Inha University, Incheon 402-751, Korea.

出版信息

J Ind Microbiol Biotechnol. 2009 Jul;36(7):993-8. doi: 10.1007/s10295-009-0580-5. Epub 2009 May 1.

Abstract

Comparative transcriptome analysis has revealed several acidic pH shock-induced genes presumably involved with stimulation of antibiotic production by S. coelicolor (Kim et al. Appl Microbiol Biotechnol 2007). Streptomyces sp. CK4412 produces a novel T cell-specific immunosuppressive compound, tautomycetin (TMC). When cultured at acidic pH medium, it also exhibited higher TMC productivity. To verify a gene responsible for acidic pH shock-induced TMC stimulation, a putative acid-shock-induced gene, SCO7832 encoding an Na(+)/H(+) antiporter protein, was cloned under the influence of a strong constitutive ermE* promoter in an integrative expression pSET152 vector. This was followed by its conjugation into the TMC-producing Streptomyces sp. CK4412. Comparing TMC production and antifungal activity of wild-type and the SCO7832-containing exconjugant revealed that SCO7832 stimulated TMC production more than 3.5-fold in Streptomyces sp. CK4412. The over-expression of SCO7832 did not affect the ratio between intra- and extra-cellular TMC productions. However, it significantly stimulated the expression of a TMC-specific positive regulatory gene. This implies that the stimulatory effect of SCO7832 functions in TMC-producing Streptomyces sp. CK4412 via up-regulation of a TMC pathway-specific positive regulatory gene, tmcN overexpression.

摘要

比较转录组分析揭示了几个酸性pH冲击诱导的基因,推测这些基因参与了天蓝色链霉菌抗生素生产的刺激过程(Kim等人,《应用微生物学与生物技术》,2007年)。链霉菌CK4412产生一种新型的T细胞特异性免疫抑制化合物,陶霉菌素(TMC)。当在酸性pH培养基中培养时,它也表现出更高的TMC产量。为了验证负责酸性pH冲击诱导TMC刺激的基因,一个假定的酸冲击诱导基因SCO7832,编码一种Na(+)/H(+)反向转运蛋白,在整合表达pSET152载体中强组成型ermE*启动子的影响下被克隆。随后将其接合到产生TMC的链霉菌CK4412中。比较野生型和含有SCO7832的接合后体的TMC产量和抗真菌活性,发现SCO7832在链霉菌CK4412中刺激TMC产量增加了3.5倍以上。SCO7832的过表达不影响细胞内和细胞外TMC产量的比例。然而,它显著刺激了TMC特异性正调控基因的表达。这意味着SCO7832的刺激作用通过上调TMC途径特异性正调控基因tmcN的过表达,在产生TMC的链霉菌CK4412中发挥作用。

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