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Assessment of Culturable Tea Rhizobacteria Isolated from Tea Estates of Assam, India for Growth Promotion in Commercial Tea Cultivars

机译:从印度阿萨姆邦茶园分离的可培养茶根瘤菌的评估,以促进商业茶品种的生长

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In the present study, 217 rhizobacterial isolates were obtained from six different tea estates of Assam, India and subjected to preliminary in vitro plant growth promotion (PGP) screening for indole acetic acid (IAA) production, phosphate solubilization, siderophore production and ammonia production. Fifty isolates showed all the PGP traits and five isolates did not exhibit any PGP traits. These 50 potential isolates were further analyzed for quantitative estimation of the PGP traits along with the aminocyclopropane-1-carboxylate (ACC) deaminase, protease and cellulose production. After several rounds of screening, four rhizobacteria were selected based on their maximum ability to produce in vitro PGP traits and their partial 16S rRNA gene sequence analysis revealed that they belong to Enterobacter lignolyticus strain TG1, Burkholderia sp. stain TT6, Bacillus pseudomycoides strain SN29 and Pseudomonas aeruginosa strain KH45. To evaluate the efficacy of these four rhizobacteria as plant growth promoters, three different commercially important tea clones TV1, TV19, and TV20 plants were inoculated with these rhizobacteria in greenhouse condition and compared to the uninoculated control plants. Though, all the rhizobacterial treatments showed an increase in plant growth compared to control but the multivariate PCA analysis confirmed more growth promotion by TG1 and SN29 strains than the other treatments in all three clones. To validate this result, the fold change analysis was performed and it revealed that the tea clone TV19 plants inoculated with the E. lignolyticus strain TG1 showed maximum root biomass production with an increase in 4.3-fold, shoot biomass with increase in 3.1-fold, root length by 2.2-fold and shoot length by 1.6-fold. Moreover, two way ANOVA analysis also revealed that rhizobacterial treatment in different tea clones showed the significant increase ( P < 0.05) in growth promotion compared to the control. Thus, this study indicates that the potential of these indigenous plant growth promoting rhizobacteria isolates to use as microbial inoculation or biofertilizer for growth promotion of tea crops.
机译:在本研究中,从印度阿萨姆邦的六个不同茶园中获得了217个根瘤菌分离株,并对其进行了初步的体外植物生长促进(PGP)筛选,以检测吲哚乙酸(IAA)的产生,磷酸盐的增溶作用,铁载体的产生和氨的产生。五十株分离株显示出所有PGP性状,五株分离株未显示出任何PGP性状。进一步分析了这50种潜在分离株,以定量评估PGP性状以及氨基环丙烷-1-羧酸酯(ACC)脱氨酶,蛋白酶和纤维素的产生。经过几轮筛选后,根据其产生体外PGP性状的最大能力选择了四个根瘤菌,其部分16S rRNA基因序列分析表明它们属于溶肠肠杆菌TG1,伯克霍尔德菌属。染色TT6,假芽胞杆菌菌株SN29和铜绿假单胞菌菌株KH45。为了评估这四种根瘤菌作为植物生长促进剂的功效,在温室条件下用这些根瘤菌接种了三种不同的商业上重要的茶克隆TV1,TV19和TV20植物,并与未接种的对照植物进行了比较。虽然,所有根瘤菌处理均显示出与对照相比植物生长加快,但是多变量PCA分析证实,TG1和SN29菌株比所有三个克隆中的其他处理均促进了更多的生长。为了验证该结果,进行了倍数变化分析,结果表明,接种木溶大肠杆菌TG1的茶克隆TV19植物显示最大根生物量产生,增加了4.3倍,芽生物量增加了3.1倍,根长为2.2倍,枝条长为1.6倍。此外,两种方差分析还显示,与对照相比,不同茶克隆中的根瘤菌处理显示出促进生长的显着增加(P <0.05)。因此,这项研究表明,这些促进原生植物生长的根瘤菌分离物可用作微生物接种或生物肥料来促进茶作物的生长。

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