Gao Tantan, Li Yan, Ding Mingzheng, Chai Yunrong, Wang Qi
Department of Plant Pathology, College of Plant Protection, China Agricultural University, Beijing 100193, China; Department of Biology, Northeastern University, 360 Huntington Avenue, Boston, MA 02215, USA.
Department of Plant Pathology, College of Plant Protection, China Agricultural University, Beijing 100193, China.
Res Microbiol. 2017 Jul-Aug;168(6):524-535. doi: 10.1016/j.resmic.2017.04.003. Epub 2017 May 4.
Plant growth-promoting rhizobacteria effectively enhance plant growth and root colonization by the bacteria is a prerequisite during the process. Bacillus cereus 905, a rhizosphere bacterium originally isolated from wheat roots, colonizes the wheat rhizosphere with a large population size. We previously showed that a manganese-containing superoxide dismutase (MnSOD2), encoded by the sodA2 gene, plays an important role in colonization of the wheat rhizosphere by B. cereus 905. In this study, we identified a gene, ptsI, which positively regulates transcription of sodA2. ptsI encodes Enzyme I of the phosphotransferase system (PTS), a major regulator of carbohydrate uptake in bacteria. Assays of β-galactosidase activity and real-time quantitative PCR showed that loss of ptsI caused a 70% reduction in sodA2 expression. The ΔptsI mutant also showed a 1000-fold reduction in colonization of wheat roots, as well as a reduced growth rate in minimal media with either glucose or succinate as the sole carbon source. Artificial induction of sodA2 in the ΔptsI mutant partially restored root colonizing ability and utilization of succinate, but not glucose. These results suggest that the PTS plays an important role in rhizosphere colonization by both promoting nutrient utilization and regulating sodA2 expression in B. cereus 905.
促进植物生长的根际细菌能有效促进植物生长,而细菌在根际的定殖是这一过程的前提条件。蜡样芽孢杆菌905是一种最初从小麦根部分离得到的根际细菌,能在小麦根际大量定殖。我们之前表明,由sodA2基因编码的含锰超氧化物歧化酶(MnSOD2)在蜡样芽孢杆菌905定殖小麦根际过程中起重要作用。在本研究中,我们鉴定出一个基因ptsI,它正向调控sodA2的转录。ptsI编码磷酸转移酶系统(PTS)的酶I,PTS是细菌碳水化合物摄取的主要调节因子。β-半乳糖苷酶活性测定和实时定量PCR结果显示,ptsI缺失导致sodA2表达降低70%。ΔptsI突变体在小麦根际的定殖能力也降低了1000倍,并且在以葡萄糖或琥珀酸作为唯一碳源的基本培养基中的生长速率也降低。在ΔptsI突变体中人工诱导sodA2可部分恢复其根际定殖能力和对琥珀酸的利用,但不能恢复对葡萄糖的利用。这些结果表明,PTS通过促进养分利用和调节蜡样芽孢杆菌905中sodA2的表达,在根际定殖中起重要作用。