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ssuA基因敲除对生防菌吡咯伯克霍尔德氏菌JK-SH007定殖和生防功能的影响

Effect of ssuA gene knockout on the colonization and biocontrol function of the biocontrol bacterium Burkholderia pyrrocinia JK-SH007

  • 摘要: 吡咯伯克霍尔德氏菌Burkholderia pyrrocinia JK-SH007是一株对杨树溃疡病具有良好防治效果的内生生防菌。基于JK-SH007菌株基因组数据设计特异性引物进行ssuA基因克隆,利用生物信息学分析ssuA蛋白与其他物种同源蛋白的相似性、系统进化和理化性质,并使用同源重组双交换获得JK-SH007菌株ssuA基因敲除株(JK-SH007∆ssuA)。在此基础上,分别测定野生株(WT)和敲除株的生长曲线、运动能力、胞外多糖、产嗜铁素、cyclic Dimeric Guanosine Monophosphate(c-di-GMP)、生物膜形成、抗菌能力、prn基因簇组成基因的表达及内生定殖动态。结果显示:ssuA基因序列全长1107 bp,编码366个氨基酸,其编码的蛋白质二级结构及三级结构元件一致;系统发育分析发现,ssuA蛋白质与Burkholderia arboris亲缘关系最近;∆ssuA菌株的胞外多糖合成、生物膜形成、产嗜铁素以及抑菌能力较WT减弱,但生长能力未发生改变;prnAprnB显著下调,而prnCprnD上调;c-di-GMP含量减少4.97%;在杨树组培苗根、茎和叶的内生定殖能力分别下降78.57%、80.77%和66.67%。因此,ssuA基因正调控JK-SH007菌株生物膜形成,与胞外多糖产生、产嗜铁素和c-di-GMP合成密切相关,同时影响抑菌能力和内生定殖能力,但对菌株生长无影响。这为揭示ssuA基因对JK-SH007菌株定殖和生防能力的影响奠定了基础,也为杨树溃疡病生防微生物菌剂的研发与高效应用提供了科学依据。

     

    Abstract: Burkholderia pyrrocinia JK-SH007 is an effective biocontrol agent against poplar canker. Based on the genomic data of JK-SH007 strain, specific primers were designed to clone the ssuA gene, and bioinformatics were used to analyze the similarity, phylogeny, and physicochemical properties of the ssuA protein to homologous proteins of other species, and the ssuA knockout mutant of JK-SH007(JK-SH007∆ssuA) was obtained by double crossover of homologous recombination. On this basis, the growth curve, motility, exopolysaccharide, siderophore production, cyclic Dimeric Guanosine Monophosphate (c-di-GMP), biofilm formation, antibacterial ability, expression of prn gene cluster and endophytic colonization dynamics of wild-type strain (WT) and knockout strain were determined. The results showed that the full-length sequence of ssuA gene is 1107 bp, encoding 366 amino acids, and the secondary structure and tertiary structure of the encoded protein are identical. Phylogenetic analysis showed that the ssuA protein was the most closely related to Burkholderia arboris. The exopolysaccharide synthesis, biofilm formation, siderophore production and antibacterial ability of the ∆ssuA strain were weaker than those of WT, but the growth ability was not changed. Two genes (prnA and prnB) were significantly down-regulated, while prnC and prnD were up-regulated. The content of c-di-GMP decreased by 4.97%. The endophtic colonization ability of roots, stems and leaves of poplar tissue-cultured seedlings decreased by 78.57%, 80.77% and 66.67%, respectively. Therefore, the ssuA gene positively regulated biofilm formation of JK-SH007, which was closely related to exopolysaccharide production, siderophore production and c-di-GMP synthesis, and affected the antibacterial ability and endogenous colonization ability, but had no effect on the growth of the strain. This study lays a foundation for revealing the effect of ssuA gene on the colonization and biocontrol ability of strain JK-SH007, and also provides a scientific basis for the development and efficient application of biocontrol microbial agents for poplar canker disease.

     

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