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在纤维弧菌中发现的强启动子的一些新特征。

Some novel features of strong promoters discovered in Cytophaga hutchinsonii.

机构信息

State Key Laboratory of Microbial Technology, Shandong University, Qingdao, 266200, China.

School of Life Science, Qilu Normal University, Jinan, 250200, China.

出版信息

Appl Microbiol Biotechnol. 2022 Apr;106(7):2529-2540. doi: 10.1007/s00253-022-11869-3. Epub 2022 Mar 23.

Abstract

Cytophaga hutchinsonii is an important Gram-negative bacterium belonging to the Bacteroides phylum that can efficiently degrade cellulose. But the promoter that mediates the initiation of gene transcription has been unknown for a long time. In this study, we determined the transcription start site (TSS) of C. hutchinsonii by 5' rapid amplification of cDNA ends (5'RACE). The promoter structure was first identified as TAAT and TATTG which are located -5 and -31 bp upstream of TSS, respectively. The function of -5 and -31 regions and the spacer length of the promoter P were explored by site directed ligase-independent mutagenesis (SLIM). The results showed that the promoter activities were sharply decreased when the TTG motif was mutated into guanine (G) or cytosine (C). Interestingly, we found that the strong promoter was accompanied with many TTTG motifs which could enhance the promoter activities within certain copies. These characteristics were different from other promoters of Bacteriodes species. Furthermore, we carried out genome scanning analysis for C. hutchinsonii and another Bacteroides species by Perl6.0. The results indicated that the promoter structure of C. hutchinsonii possessed more unique features than other species. Also, the screened inducible promoter P was used to overexpress protein CHU_2196 with a molecular weight of 120 kDa in C. hutchinsonii. The present study enriched the promoter structure of Bacteroidetes species and also provided a novel method for the highly expressed large protein (cellulase) in vivo, which was helpful to elucidate the unique cellulose degradation mechanism of C. hutchinsonii.Key points• The conserved structure of strong promoter of C. hutchinsonii was elucidated.• Two novel regulation motifs of TTTG and AATTATG in the promoter were discovered.• A new method for induced expression of cellulase in vivo was established.• Helpful for explained the unique cellulose degradation mechanism of C. hutchinsonii.

摘要

纤维弧菌是一种重要的革兰氏阴性细菌,属于拟杆菌门,可以有效地降解纤维素。但是,介导基因转录起始的启动子长期以来一直未知。在本研究中,我们通过 5' 快速扩增 cDNA 末端 (5'RACE) 确定了纤维弧菌的转录起始位点 (TSS)。启动子结构首先被鉴定为 TAAT 和 TATTG,它们分别位于 TSS 的上游-5 和-31bp。通过位点定向非连接酶诱变 (SLIM) 探索了-5 和-31 区域以及启动子 P 的间隔长度的功能。结果表明,当 TTG 基序突变为鸟嘌呤 (G) 或胞嘧啶 (C) 时,启动子活性急剧下降。有趣的是,我们发现强启动子伴随着许多 TTTG 基序,可以在一定的拷贝数内增强启动子活性。这些特征与其他拟杆菌属物种的启动子不同。此外,我们通过 Perl6.0 对纤维弧菌和另一种拟杆菌属物种进行了基因组扫描分析。结果表明,纤维弧菌的启动子结构比其他物种具有更多独特的特征。此外,筛选出的诱导启动子 P 用于在纤维弧菌中过表达分子量为 120kDa 的蛋白 CHU_2196。本研究丰富了拟杆菌属物种的启动子结构,也为体内高表达大蛋白(纤维素酶)提供了一种新方法,有助于阐明纤维弧菌独特的纤维素降解机制。

关键点

• 阐明了纤维弧菌强启动子的保守结构。

• 在启动子中发现了两个新的调节基序 TTTG 和 AATTATG。

• 建立了一种在体内诱导表达纤维素酶的新方法。

• 有助于解释纤维弧菌独特的纤维素降解机制。

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