Exploiting CotA laccase from Antarctic Bacillus sp. PAMC28748 for efficient mediator-assisted dye decolorization and ABTS regeneration

IF 8.1 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Chemosphere Pub Date : 2025-03-01 Epub Date: 2025-01-22 DOI:10.1016/j.chemosphere.2025.144137
Jayram Karmacharya , Prasansah Shrestha , So-Ra Han , Jun Hyuck Lee , Tae-Jin Oh
{"title":"Exploiting CotA laccase from Antarctic Bacillus sp. PAMC28748 for efficient mediator-assisted dye decolorization and ABTS regeneration","authors":"Jayram Karmacharya ,&nbsp;Prasansah Shrestha ,&nbsp;So-Ra Han ,&nbsp;Jun Hyuck Lee ,&nbsp;Tae-Jin Oh","doi":"10.1016/j.chemosphere.2025.144137","DOIUrl":null,"url":null,"abstract":"<div><div>Laccases are of particular interest in addressing environmental challenges, such as the degradation of triphenylmethane (TPM) dyes, including crystal violet (CV) and Coomassie Brilliant Blue (CBB), which are commonly used in SDS-PAGE for protein visualization. However, these dyes present significant environmental concerns due to their resistance to degradation, which makes their removal from industrial wastewater a major challenge. To address this, the current study investigates the potential of a novel CotA laccase derived from <em>Bacillus</em> sp. PAMC28748, an Antarctic bacterial isolate, for decolorizing these stubborn dyes. The CotA gene was successfully cloned and expressed, and the enzyme demonstrated optimal activity at pH 3 and 50 °C, which favors its maximum catalytic performance. The recombinant <em>Bacillus</em> sp. PAMC28748 rBCLac effectively decolorized CBB without additional mediators, whereas the degradation of CV required the use of the redox mediator ABTS. With ABTS, over 90 % decolorization was achieved at a 0.35 % concentration of CV after 240 min of incubation. Further investigation through molecular docking studies revealed that hydrogen bonding and hydrophobic interactions between the enzyme and the dye molecules are critical for effective degradation, highlighting the enzyme's specific interaction mechanisms. In addition to its catalytic effectiveness, the study also demonstrated the practical potential of the rBCLac system by recovering and reusing both ABTS and rBCLac through ultracentrifugation and acetone precipitation. The process maintained over 75 % efficiency across three cycles, despite a slight decline in enzyme activity, thus showcasing the system's sustainability and reusability. These findings collectively suggest that rBCLac, isolated from an extreme Antarctic environment, holds considerable promise as a candidate for the removal of industrial wastewater containing persistent dyes, with the added potential for cost-effective and sustainable water treatment through the reuse of both the enzyme and its mediator.</div></div>","PeriodicalId":276,"journal":{"name":"Chemosphere","volume":"372 ","pages":"Article 144137"},"PeriodicalIF":8.1000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemosphere","FirstCategoryId":"93","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0045653525000785","RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/22 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Laccases are of particular interest in addressing environmental challenges, such as the degradation of triphenylmethane (TPM) dyes, including crystal violet (CV) and Coomassie Brilliant Blue (CBB), which are commonly used in SDS-PAGE for protein visualization. However, these dyes present significant environmental concerns due to their resistance to degradation, which makes their removal from industrial wastewater a major challenge. To address this, the current study investigates the potential of a novel CotA laccase derived from Bacillus sp. PAMC28748, an Antarctic bacterial isolate, for decolorizing these stubborn dyes. The CotA gene was successfully cloned and expressed, and the enzyme demonstrated optimal activity at pH 3 and 50 °C, which favors its maximum catalytic performance. The recombinant Bacillus sp. PAMC28748 rBCLac effectively decolorized CBB without additional mediators, whereas the degradation of CV required the use of the redox mediator ABTS. With ABTS, over 90 % decolorization was achieved at a 0.35 % concentration of CV after 240 min of incubation. Further investigation through molecular docking studies revealed that hydrogen bonding and hydrophobic interactions between the enzyme and the dye molecules are critical for effective degradation, highlighting the enzyme's specific interaction mechanisms. In addition to its catalytic effectiveness, the study also demonstrated the practical potential of the rBCLac system by recovering and reusing both ABTS and rBCLac through ultracentrifugation and acetone precipitation. The process maintained over 75 % efficiency across three cycles, despite a slight decline in enzyme activity, thus showcasing the system's sustainability and reusability. These findings collectively suggest that rBCLac, isolated from an extreme Antarctic environment, holds considerable promise as a candidate for the removal of industrial wastewater containing persistent dyes, with the added potential for cost-effective and sustainable water treatment through the reuse of both the enzyme and its mediator.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
利用南极芽孢杆菌PAMC28748中CotA漆酶进行高效染料脱色和ABTS再生。
漆酶在解决环境挑战方面特别有兴趣,例如降解三苯甲烷(TPM)染料,包括结晶紫(CV)和考马斯亮蓝(CBB),这两种染料通常用于SDS-PAGE蛋白可视化。然而,这些染料由于其抗降解性而呈现出显著的环境问题,这使得它们从工业废水中去除成为一个主要挑战。为了解决这个问题,目前的研究调查了从芽孢杆菌sp. PAMC28748(一种南极细菌分离物)中提取的新型CotA漆酶对这些顽固染料脱色的潜力。成功克隆并表达了CotA基因,酶在pH 3和50℃条件下表现出最佳的活性,有利于其最大的催化性能。重组芽孢杆菌sp. PAMC28748 rBCLac无需额外介质即可有效脱色CBB,而降解CV则需要使用氧化还原介质ABTS。使用ABTS,在0.35%的CV浓度下,孵育240分钟后脱色率达到90%以上。通过分子对接研究进一步发现,酶与染料分子之间的氢键和疏水相互作用是有效降解的关键,突出了酶的特定相互作用机制。除了催化效果外,本研究还通过超离心和丙酮沉淀法对ABTS和rBCLac进行回收再利用,展示了rBCLac系统的实用潜力。尽管酶活性略有下降,但该过程在三个循环中保持了75%以上的效率,从而展示了系统的可持续性和可重用性。这些发现共同表明,从南极极端环境中分离出来的rBCLac,作为去除含持久性染料的工业废水的候选物,具有相当大的前景,并且通过酶及其介质的再利用,具有成本效益和可持续水处理的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Chemosphere
Chemosphere 环境科学-环境科学
CiteScore
15.80
自引率
8.00%
发文量
4975
审稿时长
3.4 months
期刊介绍: Chemosphere, being an international multidisciplinary journal, is dedicated to publishing original communications and review articles on chemicals in the environment. The scope covers a wide range of topics, including the identification, quantification, behavior, fate, toxicology, treatment, and remediation of chemicals in the bio-, hydro-, litho-, and atmosphere, ensuring the broad dissemination of research in this field.
期刊最新文献
Comparative assessment of MP effects on pigment composition and lipid profiles in three marine microalgae Phenanthrene sorption in expanded polystyrene microplastics and environmental aging effects: A Venezuelan caribbean beaches case study Effect of combined copper, salt and plant growth promoting rhizobacteria inoculation on the growth, photosynthesis and ion accumulation in the halophyte Salicornia ramosissima: a phytoremediation perspective Significantly enhanced Fenton-like degradation activity over oxygen vacancies introduced FeOOH through synergistic effect between active species Unraveling mercury dynamics in shallow lakes: Evidence from a pristine oligotrophic lake in a natural mercury hotspot of the Patagonian Andes
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1