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内生真菌草酸青霉 B4 对三氯生的高效降解

Efficient degradation of triclosan by an endophytic fungus Penicillium oxalicum B4.

机构信息

College of Pharmaceutical Sciences, Soochow University, Suzhou, 215123, China.

Institute of Medicinal Plants, Yunnan Academy of Agricultural Sciences, Kunming, 650205, China.

出版信息

Environ Sci Pollut Res Int. 2018 Mar;25(9):8963-8975. doi: 10.1007/s11356-017-1186-5. Epub 2018 Jan 13.

Abstract

Triclosan (TCS), a widely used antimicrobial and preservative agent, is an emerging contaminant in aqueous and soil environment. Microbial degradation of TCS has not been reported frequently because of its inhibition of microbe growth. To explore the new microbial resources for TCS biodegradation, fungal endophytes were isolated and screened for the degradation potential. The endophytic strain B4 isolated from Artemisia annua L. showed higher degradation efficiency and was identified as Penicillium oxalicum based on its morphology and ITS sequences of ribosomal DNA. In both medium and synthetic wastewater, TCS (5 mg/L) was almost completely degraded within 2 h by the strain B4. The high capacity of TCS uptake (127.60 ± 8.57 mg/g dry weight, DW) of fungal mycelium was observed during the first 10 min after TCS addition. B4 rapidly reduced initial content (5.00 mg/L) of TCS to 0.41 mg/L in medium in 10 min. Then, the accumulation of TCS in mycelium was degraded from 0.45 to 0.05 mg/g DW after 1-h treatment. The degradation metabolites including 2-chlorohydroquinone, 2, 4-dichloropheno, and hydroquinone were found to be restrained in mycelia. The end products of the biodegradation in medium showed no toxicity to Escherichia coli. The new characteristics of high adsorption, fast degradation, and low residual toxicity highlight the potential of endophytic P. oxalicum B4 in TCS bioremediation.

摘要

三氯生(TCS)是一种广泛使用的抗菌和防腐剂,是水和土壤环境中的一种新兴污染物。由于其对微生物生长的抑制作用,TCS 的微生物降解并未得到广泛报道。为了探索 TCS 生物降解的新微生物资源,从青蒿中分离和筛选了具有降解潜力的内生真菌。从青蒿中分离出的内生菌 B4 对 TCS 具有较高的降解效率,根据其形态和核糖体 DNA 的 ITS 序列,被鉴定为草酸青霉。在培养基和合成废水中,B4 菌株在 2 小时内几乎完全降解了 5mg/L 的 TCS。在 TCS 加入后的前 10 分钟内,真菌菌丝体对 TCS 的高吸收能力(127.60±8.57mg/g 干重,DW)被观察到。B4 在 10 分钟内将培养基中初始含量(5.00mg/L)的 TCS 迅速降低至 0.41mg/L。然后,在 1 小时的处理后,TCS 在菌丝体中的积累从 0.45mg/g DW 降解至 0.05mg/g DW。在培养基中生物降解的代谢产物包括 2-氯对苯二酚、2,4-二氯苯酚和对苯二酚被发现被限制在菌丝体中。生物降解的中间产物在培养基中对大肠杆菌没有毒性。高吸附、快速降解和低残留毒性的新特性突出了内生草酸青霉 B4 在 TCS 生物修复中的潜力。

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