多粘类芽孢杆菌吲哚-3-乙酸合成途径的鉴定及组合工程。

Huimin Sun, Jikun Zhang, Wenteng Liu, Wenhui E, Xin Wang, Hui Li, Yanru Cui, Dongying Zhao, Kai Liu, Binghai Du, Yanqin Ding, Chengqiang Wang
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引用次数: 6

摘要

背景:多粘类芽孢杆菌(Paenibacillus polymyxa)是一种典型的植物促生根杆菌(PGPR),吲哚-3-乙酸(IAA)的合成是其促生能力的原因之一。多粘木中IAA的合成途径必须进行鉴定和修饰。结果:多粘菌SC2及其突变体SC2- m1可通过直接分泌IAA促进植物生长。通过代谢组学和基因组学分析,预测了菌株SC2-M1 IAA合成天然IPyA途径中的基因patA、ilvB3和fusE。合理选择新型强启动子P04420,对其进行综合分析,评价其表达IAA合成基因的能力。在菌株SC2-M1中,patA、ilvB3和fusE三个基因的共表达使IAA产量提高了60%。此外,选择IAA合成途径的异质基因IAM和两个异质IPyA途径提高菌株SC2-M1的IAA产量。通过启动子P04420在菌株SC2-M1中表达了路德维希肠杆菌JP6全IPyA途径的ELJP6_14505、ipdC和ELJP6_00725基因,使工程菌株SC2-M1的IAA产量从13 μg/mL提高到31 μg/mL,提高了138%。结论:本研究结果有助于揭示和完善多粘草IAA合成途径及其应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Identification and combinatorial engineering of indole-3-acetic acid synthetic pathways in Paenibacillus polymyxa.

Identification and combinatorial engineering of indole-3-acetic acid synthetic pathways in Paenibacillus polymyxa.

Identification and combinatorial engineering of indole-3-acetic acid synthetic pathways in Paenibacillus polymyxa.

Identification and combinatorial engineering of indole-3-acetic acid synthetic pathways in Paenibacillus polymyxa.

Background: Paenibacillus polymyxa is a typical plant growth-promoting rhizobacterium (PGPR), and synthesis of indole-3-acetic acid (IAA) is one of the reasons for its growth-promoting capacity. The synthetic pathways of IAA in P. polymyxa must be identified and modified.

Results: P. polymyxa SC2 and its spontaneous mutant SC2-M1 could promote plant growth by directly secreting IAA. Through metabonomic and genomic analysis, the genes patA, ilvB3, and fusE in the native IPyA pathway of IAA synthesis in strain SC2-M1 were predicted. A novel strong promoter P04420 was rationally selected, synthetically analyzed, and then evaluated on its ability to express IAA synthetic genes. Co-expression of three genes, patA, ilvB3, and fusE, increased IAA yield by 60% in strain SC2-M1. Furthermore, the heterogeneous gene iaam of the IAM pathway and two heterogeneous IPyA pathways of IAA synthesis were selected to improve the IAA yield of strain SC2-M1. The genes ELJP6_14505, ipdC, and ELJP6_00725 of the entire IPyA pathway from Enterobacter ludwigii JP6 were expressed well by promoter P04420 in strain SC2-M1 and increased IAA yield in the engineered strain SC2-M1 from 13 to 31 μg/mL, which was an increase of 138%.

Conclusions: The results of our study help reveal and enhance the IAA synthesis pathways of P. polymyxa and its future application.

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