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通过 abrB 基因敲除增强解淀粉芽孢杆菌 SQR9 的根定植和生防活性。

Enhanced root colonization and biocontrol activity of Bacillus amyloliquefaciens SQR9 by abrB gene disruption.

机构信息

Jiangsu Key Lab for Solid Organic Waste Utilization, College of Resources and Environmental Science, Nanjing Agricultural University, 210095, Nanjing, China.

出版信息

Appl Microbiol Biotechnol. 2013 Oct;97(19):8823-30. doi: 10.1007/s00253-012-4572-4. Epub 2012 Nov 30.

Abstract

Root colonization by antagonistic bacteria is a prerequisite for successful biological control, and the instability of colonization under varying environmental conditions has accentuated the need to improve the colonization activity. Root colonization by Bacillus spp. is mainly determined by chemotaxis and biofilm formation, and both functions are negatively controlled by the global transcription regulator AbrB. Here, we disrupted the gene abrB in Bacillus amyloliquefaciens SQR9, which has been proven to be a promising biocontrol agent of cucumber and watermelon wilt disease. Chemotaxis, biofilm formation, and colonization activities as well as biocontrol efficiency were measured and compared between the wild-type strain of SQR9 and the abrB mutant. The data presented in this article demonstrate that the colonization and biocontrol activity of B. amyloliquefaciens SQR9 could be significantly improved by abrB gene disruption. The results offer a new strategy to enhance the biocontrol efficacy of B. amyloliquefaciens SQR9.

摘要

拮抗细菌的根定植是成功进行生物防治的前提,而在不同环境条件下定植的不稳定性加剧了提高定植活性的必要性。芽孢杆菌属的根定植主要取决于趋化作用和生物膜的形成,这两种功能都受到全局转录调节剂 AbrB 的负调控。在这里,我们敲除了已被证明是黄瓜和西瓜枯萎病有前途的生物防治剂的解淀粉芽孢杆菌 SQR9 中的 abrB 基因。趋化性、生物膜形成和定植活性以及生物防治效率在 SQR9 的野生型菌株和 abrB 突变体之间进行了测量和比较。本文提供的数据表明,通过 abrB 基因敲除可以显著提高解淀粉芽孢杆菌 SQR9 的定植和生物防治活性。该结果为提高解淀粉芽孢杆菌 SQR9 的生物防治效果提供了一种新策略。

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