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从印度高知县分离出的土壤细菌的抗菌活性及其分子鉴定。

Antibacterial activity of soil bacteria isolated from Kochi, India and their molecular identification.

作者信息

Gislin Davis, Sudarsanam Dorairaj, Antony Raj Gnanaprakasam, Baskar Kathirvelu

机构信息

Department of Advanced Zoology & Biotechnology, Loyola College, Chennai 600 034, Tamil Nadu, India.

Optimurz Bio & IT Solutions, Shenoy Nagar West, Chennai 600 030, Tamil Nadu, India.

出版信息

J Genet Eng Biotechnol. 2018 Dec;16(2):287-294. doi: 10.1016/j.jgeb.2018.05.010. Epub 2018 Jun 14.

Abstract

The present study, deal about the antibiosis activity of soil bacteria, isolated from 10 different locations of rhizosphere and diverse cultivation at Kochi, Kerala, India. The bacteria were isolated by standard serial dilution plate techniques. Morphological characterization of the isolate was done by Gram's staining and found that all of them gram positive. Isolated bacteria were tested against 6 human pathogens , sp., , , and sp. Primary screening was carried out by perpendicular streaking and seed overlay method. Based on the result of primary screening most potential isolates of S1A1 and S7A3 were selected for secondary screening. Both the isolates showed positive results against sp. and . The maximum antagonistic activity of 20.98 and 27.08 mm zone of inhibition was recorded at S1A1 against sp. and respectively, at 180 µl concentration. Molecular identification was carried out by 16S rRNA sequence. The 16S rRNA was amplified from the DNA samples by using PCR. The amplified 16S rRNA PCR products were purified and sequenced. The sequences were subjected to NCBI BLAST. The isolates S1A1 and S7A3 BLAST results showed 99% and 95% respectively, similarity with the available database sequence of . The sequences were deposited in GenBank and the accession numbers KY864390 (S1A1) and KY880975 (S7A3) were obtained.

摘要

本研究涉及从印度喀拉拉邦高知10个不同根际位置和不同栽培环境中分离出的土壤细菌的抗菌活性。通过标准系列稀释平板技术分离细菌。通过革兰氏染色对分离菌株进行形态学鉴定,发现它们均为革兰氏阳性。对分离出的细菌针对6种人类病原体进行测试,分别为 、 、 、 、 和 。通过垂直划线和种子覆盖法进行初步筛选。基于初步筛选结果,选择了最具潜力的分离株S1A1和S7A3进行二次筛选。这两种分离株对 和 均显示出阳性结果。在浓度为180µl时,S1A1对 和 的最大抑菌圈活性分别为20.98和27.08mm。通过16S rRNA序列进行分子鉴定。使用PCR从DNA样本中扩增16S rRNA。对扩增的16S rRNA PCR产物进行纯化和测序。将序列提交至NCBI BLAST。分离株S1A1和S7A3的BLAST结果显示,它们分别与现有数据库序列 具有99%和95%的相似性。序列已存入GenBank,获得的登录号分别为KY864390(S1A1)和KY880975(S7A3)。

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