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栓菌属真菌 Nectriella pironii 的漆酶活性及其在城市公园凋落叶上生产的创新策略。

Laccase activity of the ascomycete fungus Nectriella pironii and innovative strategies for its production on leaf litter of an urban park.

机构信息

Department of Industrial Microbiology and Biotechnology, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland.

Department of Environmental Engineering, Faculty of Biology and Environmental Sciences, Cardinal Stefan Wyszynski University in Warsaw, Warsaw, Poland.

出版信息

PLoS One. 2020 Apr 16;15(4):e0231453. doi: 10.1371/journal.pone.0231453. eCollection 2020.

Abstract

A laccase-producing ascomycete fungus was isolated from soil collected around the premises of a textile dye factory and identified as Nectriella pironii. Efficient laccase production was achieved via the synergistic action of 1 mM copper sulfate and ferulic acid. Extracts of rapeseed oil cake, grass hay, and leaf litter collected in a pocket urban park were used for enzyme production. The highest laccase activity (3,330 U/L) was observed in the culture grown on the leaf litter extract. This is the first report on biosynthesis of laccase by N. pironii. This is also the first study on utilization of naturally fallen park leaves as a substrate for fungal laccase production. The extracellular enzyme possessing laccase activity was purified to homogeneity by ion-exchange and gel filtration chromatographic techniques. The amino acid sequence of the protein revealed highest similarity to the laccase enzyme produced by Stachybotrys chartarum-and considerable homology to those produced by other fungal species. The purified laccase possessed a molecular mass of 50 kDa. The enzyme had an optimum pH of 2.0 or 6.0 and retained more than 50% of residual activity after 3 hours of incubation at pH 3.0-10.6 or 4.0-9.0 when 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid or 2,6-dimethoxyphenol, respectively, were used. Dithiothreitol, β-mercaptoethanol, and sodium azide at 1 mM concentration strongly inhibited the laccase activity, while in the presence of 50 mM urea, the enzyme was found to retain 25% of its activity. The laccase was able to decolorize more than 80% of Indigo Carmine, Remazol Brilliant Blue R, Reactive Orange 16, and Acid Red 27 dyes within 1 h. The possibility of leaf litter use for the production of the laccase enzyme from N. pironii (IM 6443), exhibiting high pH stability and degradative potential, makes it a promising tool for use in different environmental and industrial operations.

摘要

从纺织染料厂周围土壤中分离到一株产漆酶的子囊菌,鉴定为皮落青霉。通过 1mM 硫酸铜和阿魏酸的协同作用,实现了漆酶的高效生产。从口袋城市公园收集的菜籽油饼、草干草和落叶提取物被用于酶生产。在落叶提取物上培养的菌中观察到最高的漆酶活性(3330U/L)。这是首次报道皮落青霉生物合成漆酶。这也是首次研究利用自然凋落的公园树叶作为真菌漆酶生产的底物。具有漆酶活性的胞外酶通过离子交换和凝胶过滤色谱技术被纯化为均一性。该蛋白质的氨基酸序列与密粘褶菌产生的漆酶酶具有最高的相似性,并且与其他真菌物种产生的漆酶具有相当的同源性。纯化的漆酶具有 50kDa 的分子量。该酶的最适 pH 值为 2.0 或 6.0,在 pH 3.0-10.6 或 4.0-9.0 孵育 3 小时后,当分别使用 2,2'-联氮双(3-乙基苯并噻唑啉-6-磺酸或 2,6-二甲氧基苯酚时,保留超过 50%的残余活性。1mM 浓度的二硫苏糖醇、β-巯基乙醇和叠氮化钠强烈抑制漆酶活性,而在 50mM 脲存在下,酶保留 25%的活性。漆酶能够在 1 小时内使超过 80%的靛蓝卡玛、活性艳蓝 R、活性橙 16 和酸性红 27 染料脱色。利用皮落青霉(IM 6443)生产漆酶的可能性,该酶具有高 pH 稳定性和降解潜力,使其成为在不同环境和工业操作中应用的有前途的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c45/7162450/d9c1afe8bb23/pone.0231453.g001.jpg

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