Precise genome modification of agrobacterium based on one-step homologous recombination via endogenous transfer DNA.

IF 2.2 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Acta biochimica Polonica Pub Date : 2026-05-25 eCollection Date: 2026-01-01 DOI:10.3389/abp.2026.16599
Yu Liu, Geng Sun, Chunyan Gao, Rui Gao, Jian Tang, Menghu Wang, Jian Guo, Rui Guo
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引用次数: 0

Abstract

Here, a simple and precise genome modification method for agrobacterium was described and tested in strain GV3101. Taking the induced endogenous Transfer DNA (T-DNA) as the single-strand homologous repair template, this makes it possible to achieve valid and accurate genome modification for agrobacterium even without the strengthening of gene editing tools such as the CRISPR/Cas9 system. In addition, the introduction of tool plasmids into recipient agrobacteria can be achieved by the freeze-thaw method rather than complex triparental mating or expensive electroporation, which makes it more convenient. Here, the modification rate of agrobacterium strain GV3101 at both the upstream and downstream of VirD2 is 4.5% with 100% sequence accuracy. This research provides a valuable potential tool for genetic engineering in agrobacterium, with potential applications in biotechnology and agricultural sciences.

基于内源转移DNA一步同源重组的农杆菌精确基因组修饰。
本文描述了一种简单、精确的农杆菌基因组修饰方法,并对菌株GV3101进行了试验。以诱导内源转移DNA (induced endogenous Transfer DNA, T-DNA)作为单链同源修复模板,即使不需要加强CRISPR/Cas9系统等基因编辑工具,也可以实现对农杆菌有效、准确的基因组修饰。此外,将工具质粒引入农杆菌受体可以通过冻融法实现,而不是复杂的三亲本交配或昂贵的电穿孔,这使得它更加方便。在这里,农杆菌菌株GV3101在VirD2的上下游修饰率均为4.5%,序列准确度为100%。该研究为农杆菌基因工程提供了一种有价值的潜在工具,在生物技术和农业科学方面具有潜在的应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta biochimica Polonica
Acta biochimica Polonica 生物-生化与分子生物学
CiteScore
2.40
自引率
0.00%
发文量
99
审稿时长
4-8 weeks
期刊介绍: Acta Biochimica Polonica is a journal covering enzymology and metabolism, membranes and bioenergetics, gene structure and expression, protein, nucleic acid and carbohydrate structure and metabolism.
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