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与茶树相关的可培养内生放线菌的系统发育和功能特性研究,用于促进商业茶树品种的生长

Phylogenetic and Functional Characterization of Culturable Endophytic Actinobacteria Associated With spp. for Growth Promotion in Commercial Tea Cultivars.

作者信息

Borah Atlanta, Thakur Debajit

机构信息

Microbial Biotechnology Laboratory, Life Sciences Division, Institute of Advanced Study in Science and Technology, Guwahati, India.

出版信息

Front Microbiol. 2020 Feb 28;11:318. doi: 10.3389/fmicb.2020.00318. eCollection 2020.

Abstract

Plant associated endophytic actinobacteria may contribute to plant growth and defense by direct or indirect methods. Our aim was to evaluate the plant growth promoting and antifungal activities of endophytic actinobacteria associated with spp. and related genera, to find potent plant growth promoting strains that could be applied in future microbe based bioformulations. We isolated 46 endophytic actinobacteria based on morphological characteristics of the isolates. 16S rRNA gene sequence analysis showed that the strains represented nine actinobacterial genera, and . functional characterization of the isolates for plant growth promoting (PGP) traits revealed many potent PGP isolates such as, SA1 and S43 which showed all the tested PGP traits, i.e., phosphate solubilization, indole-3-acetic acid (IAA), ammonia, siderophore and chitinase production. Out of the 46 endophytic actinobacteria isolates, 21 showed inhibition against atleast one test fungal phytopathogen and, isolates SA25 and SA29 exhibited broad spectrum antifungal activity against all the tested phytopathogens. Most of the endophytic actinobacteria isolates having antifungal activity were positive for the presence of chitinase, NRPS (Non-ribosomal peptides synthetase) or PKS-1 (Polyketide Synthase) gene, suggesting the presence of distinctive mechanisms to inhibit the growth of pathogenic plant fungi. ARDRA (Amplified Ribosomal DNA Restriction analysis) and BOX-PCR fingerprinting analysis of the potent isolates with antagonistic activity grouped the isolates into 5 and 4 separate clusters, respectively. In addition, an assessment using bonitur scale revealed the top ranked isolates based on their PGP and biocontrol traits. Further detection of IAA production by the top ranked actinobacterial isolates namely, SA1, T1LA3 and S85 by using thin-layer chromatography (TLC), high-performance liquid chromatography (HPLC) and liquid chromatography-mass spectrometry (LC-MS) was done. Endophytic actinobacteria isolates, namely, SA1, T1LA3, and SA14 were further tested for their efficacy in promoting the growth of commercial tea clones, namely, TV1, TV9, TV18, and TV22 in nursery conditions. All the endophytic isolates tested showed significant differences ( ≤ 0.05) in terms of plant growth promoting parameters in the treated plants compared to untreated control and may, thus be, deemed as potential candidates for application in bioformulations for tea growth.

摘要

与植物相关的内生放线菌可能通过直接或间接方式促进植物生长并增强植物防御能力。我们的目的是评估与 spp. 及相关属相关的内生放线菌的植物生长促进和抗真菌活性,以寻找可应用于未来基于微生物的生物制剂中的高效植物生长促进菌株。我们根据分离株的形态特征分离出46株内生放线菌。16S rRNA基因序列分析表明,这些菌株代表9个放线菌属,即 和 。对分离株的植物生长促进(PGP)特性进行功能表征,发现了许多高效的PGP分离株,如SA1和S43,它们表现出所有测试的PGP特性,即磷酸盐溶解、吲哚 - 3 - 乙酸(IAA)、氨、铁载体和几丁质酶的产生。在46株内生放线菌分离株中,21株对至少一种测试的植物病原真菌有抑制作用,分离株SA25和SA29对所有测试的植物病原真菌表现出广谱抗真菌活性。大多数具有抗真菌活性的内生放线菌分离株的几丁质酶、非核糖体肽合成酶(NRPS)或聚酮合酶 - 1(PKS - 1)基因呈阳性,表明存在抑制植物病原真菌生长的独特机制。对具有拮抗活性的高效分离株进行扩增核糖体DNA限制性分析(ARDRA)和BOX - PCR指纹图谱分析,分别将分离株分为5个和4个单独的簇。此外,使用博尼图量表进行的评估揭示了基于其PGP和生物防治特性的排名靠前的分离株。通过薄层色谱(TLC)、高效液相色谱(HPLC)和液相色谱 - 质谱联用(LC - MS)对排名靠前的放线菌分离株SA1、T1LA3和S85的IAA产生情况进行了进一步检测。对内生放线菌分离株SA1、T1LA3和SA14在苗圃条件下促进商业茶克隆TV1、TV9、TV18和TV22生长的功效进行了进一步测试。与未处理的对照相比,所有测试的内生分离株在处理过的植物的植物生长促进参数方面均表现出显著差异(≤0.05),因此可被视为用于茶叶生长生物制剂的潜在候选菌株。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c7b/7059647/53832c9099a7/fmicb-11-00318-g001.jpg

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