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番茄根内生植物促生菌:处理番茄(L.)的分离、体外特性及体内评价

Endophytic PGPR from Tomato Roots: Isolation, In Vitro Characterization and In Vivo Evaluation of Treated Tomatoes ( L.).

作者信息

Cochard Bastien, Giroud Basile, Crovadore Julien, Chablais Romain, Arminjon Lucas, Lefort François

机构信息

Plants and Pathogens Group, Research Institute Land Nature and Environment, Geneva School of Engineering, Architecture and Landscape (HEPIA), HES-SO University of Applied Sciences and Arts Western Switzerland, 1254 Jussy, Switzerland.

出版信息

Microorganisms. 2022 Apr 1;10(4):765. doi: 10.3390/microorganisms10040765.

DOI:10.3390/microorganisms10040765
PMID:35456815
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9031218/
Abstract

Plant-growth-promoting rhizobacteria (PGPR) are soil bacteria colonizing the rhizosphere and the rhizoplane which have an effect on plant growth through multiple chemical compounds. Rhizobacteria with beneficial effects for plants could therefore be used to reduce the dependence on synthetic chemical fertilizers in conventional agriculture. Within this study, 67 endophytic fungi and 49 bacteria were isolated from root samples from 3 different commercial productions: an off-ground tomato production in a greenhouse, an organic production and a conventional production, both in a soil tunnel. Following morphological selection, 12 fungal and 33 bacterial isolates were genetically identified. Thirteen bacterial isolates belonging to nine potential PGPR species were then applied to tomato seedlings established in sterile substrate. The ability of these bacteria to produce indole acetic acid (IAA) and solubilize phosphate was also evaluated. They all were IAA producers and solubilized phosphate. The most interesting strains for growth promotion were found to be the isolates B10, B25, B29 and B17. The isolates B17, B29, B18 and B6 also increased root growth. This study proposed a quick protocol for isolating and testing potential endophytic PGPR that should be characterized further for the direct and indirect mechanisms of growth promotion.

摘要

植物促生根际细菌(PGPR)是定殖于根际和根表的土壤细菌,它们通过多种化合物对植物生长产生影响。因此,对植物有益的根际细菌可用于减少传统农业对合成化学肥料的依赖。在本研究中,从3种不同商业生产模式的根系样本中分离出67株内生真菌和49株细菌:温室离地番茄生产、有机生产以及土壤隧道中的传统生产。经过形态学筛选后,对12株真菌分离株和33株细菌分离株进行了基因鉴定。然后将属于9种潜在PGPR物种的13株细菌分离株应用于无菌基质中培育的番茄幼苗。还评估了这些细菌产生吲哚乙酸(IAA)和溶解磷的能力。它们均能产生IAA并溶解磷。发现对促进生长最具潜力的菌株是分离株B10、B25、B29和B17。分离株B17、B29、B18和B6还促进了根系生长。本研究提出了一种快速分离和测试潜在内生PGPR的方案,对于其促进生长的直接和间接机制还应进一步进行表征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30dd/9031218/09282d3ccc17/microorganisms-10-00765-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30dd/9031218/3f80e6004658/microorganisms-10-00765-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30dd/9031218/be381fd9e89a/microorganisms-10-00765-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30dd/9031218/bb813aa1cee9/microorganisms-10-00765-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30dd/9031218/04cb1562587c/microorganisms-10-00765-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30dd/9031218/625381abed5a/microorganisms-10-00765-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30dd/9031218/4ad97f4c8ef9/microorganisms-10-00765-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30dd/9031218/f388c97d326c/microorganisms-10-00765-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30dd/9031218/09282d3ccc17/microorganisms-10-00765-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30dd/9031218/3f80e6004658/microorganisms-10-00765-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30dd/9031218/be381fd9e89a/microorganisms-10-00765-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30dd/9031218/bb813aa1cee9/microorganisms-10-00765-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30dd/9031218/04cb1562587c/microorganisms-10-00765-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30dd/9031218/625381abed5a/microorganisms-10-00765-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30dd/9031218/4ad97f4c8ef9/microorganisms-10-00765-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30dd/9031218/f388c97d326c/microorganisms-10-00765-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30dd/9031218/09282d3ccc17/microorganisms-10-00765-g008.jpg

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