Budiharjo Anto, Chowdhury Soumitra Paul, Dietel Kristin, Beator Barbara, Dolgova Olga, Fan Ben, Bleiss Wilfrid, Ziegler Jörg, Schmid Michael, Hartmann Anton, Borriss Rainer
Bakteriengenetik, Institut für Biologie, Humboldt Universität Berlin, Berlin, Germany.
Research Unit Microbe-Plant Interactions, Helmholtz Zentrum München, German Research Center for Environmental Health (GmbH), Neuherberg, Germany.
PLoS One. 2014 May 21;9(5):e98267. doi: 10.1371/journal.pone.0098267. eCollection 2014.
Bacillus amyloliquefaciens ssp. plantarum FZB42 represents the prototype of Gram-positive plant growth promoting and biocontrol bacteria. In this study, we applied transposon mutagenesis to generate a transposon library, which was screened for genes involved in multicellular behavior and biofilm formation on roots as a prerequisite of plant growth promoting activity. Transposon insertion sites were determined by rescue-cloning followed by DNA sequencing. As in B. subtilis, the global transcriptional regulator DegU was identified as an activator of genes necessary for swarming and biofilm formation, and the DegU-mutant of FZB42 was found impaired in efficient root colonization. Direct screening of 3,000 transposon insertion mutants for plant-growth-promotion revealed the gene products of nfrA and RBAM_017140 to be essential for beneficial effects exerted by FZB42 on plants. We analyzed the performance of GFP-labeled wild-type and transposon mutants in the colonization of lettuce roots using confocal laser scanning microscopy. While the wild-type strain heavily colonized root surfaces, the nfrA mutant did not colonize lettuce roots, although it was not impaired in growth in laboratory cultures, biofilm formation and swarming motility on agar plates. The RBAM17410 gene, occurring in only a few members of the B. subtilis species complex, was directly involved in plant growth promotion. None of the mutant strains were affected in producing the plant growth hormone auxin. We hypothesize that the nfrA gene product is essential for overcoming the stress caused by plant response towards bacterial root colonization.
解淀粉芽孢杆菌植物亚种FZB42是革兰氏阳性植物促生和生防细菌的典型代表。在本研究中,我们应用转座子诱变来构建一个转座子文库,并筛选参与多细胞行为和根际生物膜形成的基因,这些是植物促生活性的先决条件。通过拯救克隆随后进行DNA测序来确定转座子插入位点。与枯草芽孢杆菌一样,全局转录调节因子DegU被鉴定为群体运动和生物膜形成所需基因的激活剂,并且发现FZB42的DegU突变体在有效定殖于根部方面存在缺陷。对3000个转座子插入突变体进行植物促生直接筛选,结果表明nfrA和RBAM_017140的基因产物对于FZB42对植物产生有益作用至关重要。我们使用共聚焦激光扫描显微镜分析了绿色荧光蛋白标记的野生型和转座子突变体在生菜根定殖中的表现。虽然野生型菌株大量定殖于根表面,但nfrA突变体并未定殖于生菜根,尽管它在实验室培养中的生长、生物膜形成和在琼脂平板上的群体运动方面并未受损。仅在枯草芽孢杆菌物种复合体的少数成员中出现的RBAM17410基因直接参与植物促生。没有一个突变菌株在产生植物生长激素生长素方面受到影响。我们推测nfrA基因产物对于克服植物对细菌根定殖反应所引起的应激至关重要。