印尼龙库特蜡样芽孢杆菌IrC2株苯酚生物降解及邻苯二酚2,3-双加氧酶基因测序

C. Tahya, Wahyu Irawati, F. Purba
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引用次数: 2

摘要

苯酚是一种有毒的有机化合物,对人类、哺乳动物有害,并破坏水生环境,尤其是淡水环境中的高等生物。利用细菌降解有害化学物质、解毒废水的生物降解方法是一种有效而高效的方法。从印度尼西亚东爪哇龙库特的一个工业废水处理厂的污泥中分离出蜡样芽孢杆菌IrC2,对其在低盐培养基中降解酚的能力进行了研究。蜡样芽孢杆菌IrC2是革兰氏阳性细菌。该细菌为可运动的棒状细菌,其16S rRNA基因的核苷酸序列已测序,可在GenBank中访问,登录号为MK511840。蜡样芽孢杆菌IrC2能够使用高达400ppm的苯酚作为唯一碳源,培养48小时。苯酚较初始浓度降解96%。用4-氨基安替比林试剂比色法计算苯酚的降解量,GC - MS分析证实。苯酚的好氧降解途径包括三个步骤;在第一步中,将两个羟基插入到芳香环上,由单加氧酶或双加氧酶催化生成二羟基芳香化合物,这些化合物大多是儿茶酚。儿茶酚进入由儿茶酚1,2-双加氧酶和/或儿茶酚2,3-双加氧酶催化的芳环裂解的下一步。通过PCR扩增蜡样芽孢杆菌IrC2的邻苯二酚2,3-双加氧酶基因,并将其克隆到pTA2载体上。将克隆的质粒(pTA2-catE)转化到大肠杆菌DH5α中,筛选出蓝白色菌落。采用Sanger脱氧测序法确定插入序列。蜡样芽孢杆菌IrC2的邻苯二酚2,3-双加氧酶基因核苷酸序列已录入GenBank,登录号为MK561609。
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Phenol Biodegradation and Catechol 2,3-Dioxygenase Gene Sequencing of Bacillus cereus IrC2 isolated from Rungkut Indonesia
Phenol is toxic organic compounds that harmful to humans, mammals, and disrupt the aquatic environment, especially higher-organisms in fresh-water environment. The biodegradation method using bacteria to degrade hazardous chemical and detoxify wastewater is an effective and efficient method. Bacillus cereus IrC2 isolated from sludge in an industrial wastewater treatment plant in Rungkut – East Java, Indonesia has been examined for the ability to degrade phenols in minimal salt medium. Bacillus cereus IrC2 is Gram-positive bacterium. This bacterium is motile, rod-shaped and its nucleotides sequence of 16S rRNA gene has been sequenced and can be accessed in GenBank with accession number MK511840. Bacillus cereus IrC2 is capable to use phenol up to 400 ppm as the sole carbon source to grow for 48 hours incubation. Phenol degrades 96% from initial concentration. Degradation of phenol was calculated by colorimetric method using 4-aminoantipyrine reagent and confirmed by GC MS analysis. The aerobic degradation of phenol pathways consists of three steps; in the first step, two hydroxyl groups are inserted into aromatic ring and catalyzed by mono or dioxygenase to produce dihydroxy aromatic compounds which are mostly catechols. Catechol enters the next step of aromatic ring cleavage catalyzed by catechol 1,2-dioxygenase and/or catechol 2,3- dioxygenase. The catechol 2,3-dioxygenase gene of Bacillus cereus IrC2 has been amplified by PCR and cloned into pTA2 vector. The cloned plasmid (pTA2-catE) was transformed into E. coli DH5α and selected blue-white colonies. The insert sequence was determined by Sanger deoxy sequencing method. The catechol 2,3-dioxygenase gene nucleotides sequence of Bacillus cereus IrC2 was submitted nto GenBank with accession number MK561609.
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