印尼pongkor金矿和菲律宾marinduque铜矿的抗重金属根腐菌

E. Yuniarti, I. F. Dalmacio, E. Paterno
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引用次数: 2

摘要

本研究的目的是分离、鉴定和鉴定生长在金铜矿植物根际的根际细菌。根瘤菌的分离采用无氮半固态琼脂培养基、TSA和SLP加重金属(Pb、Cd和Cu)。分离的根瘤菌对SLP培养基中较高水平的Pb、Cd、Cu具有抗性。对根细菌进行了细胞形态学、运动性、革兰氏染色和生物膜形成的培养和形态学表征。根瘤菌鉴定采用16S RNA基因片段序列分析。结果表明,铜矿区大部分根菌(21株)对铜(72150 ppm)耐药(66.7%),而金矿区大部分根菌(18株)对72 ppm铜敏感(77.8%)。土壤中大部分铜以颗粒形式附着在砾石上,不溶性较强,铜矿区的根瘤菌对有效铜有较强的适应性。这一事实解释了根菌的MIC值低于土壤中总Cu水平的原因。3种HMs抗性根瘤菌(PbSM 2.1、MGR 334和CuNFbM 4.1)形成生物膜,是HMs抗性机制之一。本研究表明,HM污染土壤比HM未污染土壤是获得耐HM根瘤菌的更好来源。使用四种分离培养基产生的根菌比每种分离培养基产生的根菌更多样化。为了获得可作为生物肥料和植物修复剂的抗HM根瘤菌,还需要进一步的鉴定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
HEAVY METAL-RESISTANT RHIZOBACTERIA FROM GOLD MINE IN PONGKOR INDONESIA AND COPPER MINE IN MARINDUQUE PHILIPPINES
The purposes of the study was to isolate, to characterize, and to identify rhizobacteria from plant rhizosphere growing in gold and copper mine. The isolation of rhizobacteria used N-free semisolid agar media, TSA, and SLP plus heavy metals (HMs), namely Pb, Cd, and or Cu. Isolated rhizobacteria were subsequently characterized for resistance to higher level of Pb, Cd, Cu in SLP media. Cultural and morphological characterization of rhizobacteria were conducted for cell morphology, motility, Gram staining, and biofilm formation. The rhizobacteria identification used sequence analysis of the 16S RNA gene fragments. The results showed that the majority of rhizobacterial from Cu mine site (66.7% of 21 isolates) were resistant to Cu (72150 ppm) while the majority of rhizobacteria from gold mine site (77.8% of 18 isolates) were sensitive to 72 ppm Cu. Majority of Cu in the soil was insoluble as granules attaching to gravel so that rhizobacteria of Cu mine site have been exposed and adapted to available Cu. This fact, explaining that the rhizobacteria’s MIC value was lower than the total Cu level in the soil. Three HMs-resistant rhizobacter (PbSM 2.1, MGR 334, and CuNFbM 4.1) formed biofilms, which was as one of the resistance mechanism to HMs. This research informed that HM contaminated-soil is better source for obtaining HM resistant rhizobacteria than HM uncontaminated-soil. The use four isolation media produce rhizobacteria which was more diverse than rhizobacteria from each isolation medium. Further characterization needs to be done to obtain HM resistant-rhizobacteria which can be used as biofertilizers and phytoremediation agent.
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