Li Qi, Yang Xiaolei, Li Jianhong, Li Mingyuan, Li Changning, Yao Tuo
Key Laboratory of Grassland Ecosystem, Ministry of Education, Sino-U.S. Centers for Grazing Land Ecosystem Sustainability, Ministry of Science and Technology, College of Pratacultural Science, Gansu Agricultural University, Lanzhou, China.
Front Microbiol. 2023 Jan 4;13:1019383. doi: 10.3389/fmicb.2022.1019383. eCollection 2022.
The use of plant growth promoting bacteria (PGPB) express phytase (-inositol hexakisphosphate phosphohydrolase) capable of hydrolyzing inositol phosphate in soil was a sustainable approach to supply available phosphorus (P) to plants. A total of 73 bacterial isolates with extracellular phytase activity were selected from seven dominant grass species rhizosphere in alpine grassland of Qinghai-Tibetan Plateau. Then, the plant growth promoting (PGP) traits of candidate bacteria were screened by qualitative and quantitative methods, including organic/inorganic Phosphorus solubilization (P. solubilization), plant hormones (PHs) production, nitrogen fixation, 1-aminocyclopropane-1-carboxylic acid (ACC) deaminase activity and antimicrobial activity. Further experiment were conducted to test their growth promoting effect on Lolium perenne L. under P-limitation. Our results indicated that these bacteria as members of phyla Proteobacteria (90.41%) and Actinobacteria (9.59%) were related to 16 different genera. The isolates of species showed the highest isolates number (36) and average values of phytase activity (0.267 ± 0.012 U mL), and showed a multiple of PGP traits, which was a great candidate for PGPBs. In addition, six strains were positive in phytase gene (β-propeller phytase, ) amplification, which significantly increased the shoot length, shoot/root fresh weight, root average diameter and root system phytase activity of L. under P-limitation, and the expression of phytase gene () in root system were verified by qPCR. Finally, the PHY101 gene encoding phytase from GS10-1 was cloned, sequenced, and recombinantly expressed in . Biochemical characterization demonstrated that the recombinant phytase PHY101 revealed the highest activity at pH 6 and 40°C temperature. In particular, more than 60% of activity was retained at a low temperature of 15°C. This study demonstrates the opportunity for commercialization of the phytase-producing PGPB to developing localized microbial inoculants and engineering rhizobacteria for sustainable use in alpine grasslands.
利用能够水解土壤中肌醇磷酸的植物促生细菌(PGPB)表达植酸酶(肌醇六磷酸磷酸水解酶)是一种向植物提供有效磷(P)的可持续方法。从青藏高原高寒草原七种优势禾本科植物根际共筛选出73株具有胞外植酸酶活性的细菌分离株。然后,通过定性和定量方法对候选细菌的植物促生(PGP)特性进行筛选,包括有机/无机磷溶解(P.溶解)、植物激素(PHs)产生、固氮、1-氨基环丙烷-1-羧酸(ACC)脱氨酶活性和抗菌活性。进行进一步实验以测试它们在磷限制条件下对多年生黑麦草的促生长作用。我们的结果表明,这些细菌作为变形菌门(90.41%)和放线菌门(9.59%)的成员,与16个不同属有关。该物种的分离株显示出最高的分离株数量(36)和植酸酶活性平均值(0.267±0.012 U mL),并表现出多种PGP特性,是PGPB的极佳候选者。此外,六株菌株在植酸酶基因(β-螺旋桨植酸酶,)扩增中呈阳性,这显著增加了磷限制条件下多年生黑麦草的地上部长度、地上部/根鲜重、根平均直径和根系植酸酶活性,并通过qPCR验证了根系中植酸酶基因()的表达。最后,从GS10-1中克隆、测序并在中重组表达了编码植酸酶的PHY101基因。生化特性表明,重组植酸酶PHY101在pH 6和40°C温度下显示出最高活性。特别是,在15°C的低温下保留了超过60%的活性。本研究证明了生产植酸酶的PGPB商业化的机会,以开发本地化微生物接种剂并改造根际细菌,以便在高寒草原可持续利用。