Identification of mercury‐resistant Streptomyces isolated from Cyperus rotundus L. rhizosphere and molecular cloning of mercury (II) reductase gene

Q4 Environmental Science
Wahyu Aristyaning Putri, Hanum Mukti Rahayu, A. Khasanah, L. Sembiring, M. Kawaichi, Y. A. Purwestri
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引用次数: 0

Abstract

Streptomyces is one of mercury‐resistant bacteria which can convert Hg2+ into nontoxic Hg0 . This study aimed to identify mercury‐resistant Streptomyces present in the Cyperus rotundus rhizosphere from artisanal small‐scale gold mining (ASGM) area and clone merA gene to the cloning and expression vectors. Molecular identification was conducted using 16s rRNA gene with the maximum likelihood algorithms. Results revealed that the AS1 and AS2 strains were a group of Streptomyces ardesiacus and the BR28 strain was closed to Brevibacillus agri. The AS2 merA gene was cloned to pMD20 cloning vectors, pGEX‐5x‐1 and pET‐28c expression vectors. The transformation was successfully performed in BL21 and DH5α competent cells. The full length of the merA gene was confirmed to be 1,425 bp. This study is the first research on identifying mercury‐resistant Streptomyces and cloning the full‐length merA gene in Indonesia.
圆柏根际耐汞链霉菌的鉴定及汞(II)还原酶基因的分子克隆
链霉菌是一种能将Hg2+转化为无毒Hg0的耐汞细菌。本研究旨在鉴定手工小规模金矿(ASGM)区圆柏根际存在的耐汞链霉菌,并将merA基因克隆到克隆和表达载体上。使用16s rRNA基因和最大似然算法进行分子鉴定。结果表明,AS1和AS2菌株是一组ardesiacus链霉菌,BR28菌株与农业短杆菌相近。将AS2-merA基因克隆到pMD20克隆载体、pGEX‐5x‐1和pET‐28c表达载体上。转化成功地在BL21和DH5α感受态细胞中进行。merA基因全长1425bp。本研究是印尼首次鉴定耐汞链霉菌并克隆全长merA基因的研究。
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来源期刊
Indonesian Journal of Biotechnology
Indonesian Journal of Biotechnology Environmental Science-Environmental Science (miscellaneous)
CiteScore
1.00
自引率
0.00%
发文量
20
审稿时长
12 weeks
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