Literature DB >> 25435502

The effect of mutations near the T1 copper site on the biochemical characteristics of the small laccase from Streptomyces coelicolor A3(2).

A Prins1, L Kleinsmidt2, N Khan3, B Kirby4, T Kudanga5, J Vollmer6, J Pleiss7, S Burton8, M Le Roes-Hill9.   

Abstract

Bacterial laccases show low activities but can be of biotechnological interest due to industrially suitable characteristics such as thermostability and tolerance to alkaline pH. In this study, three separate mutations (M298F, V290N and V290A) were introduced at or near the T1 copper site of the small laccase (SLAC) from Streptomyces coelicolor A3(2) and biochemical properties were assessed in comparison with the native enzyme. The mutation, V290N showed approximately double the activity of SLAC when ABTS was used as substrate while the specific activity of SLAC-M298F was 4-5 times higher than that of SLAC when the assays were performed at ≥70°C. There was no significant difference in activity with 2,6-dimethoxyphenol (2,6-DMP); however, there was a significant shift in the optimal pH from pH 9.5 (SLAC) to 7.5 (SLAC-V290N). Optimal temperature for activity was not significantly altered but thermostability was reduced in all three mutants. The substrate range of the mutant variants remained largely unchanged, with the exception of SLAC-M298F which was unable to oxidise veratryl alcohol. Interestingly, the "typical" laccase inhibitor, sodium azide, had no significant inhibitory effect on the activity of SLAC-M298F, which also exhibited increased resistance to inhibition by sulfhydryl compounds. SLAC-V290N showed higher catalytic efficiency for 2,6-DMP (kcat/Km=2.226mM(-1)s(-1)) and ABTS (kcat/Km=1.874mM(-1)s(-1)) compared to SLAC (kcat/Km=1.615mM(-1)s(-1) for 2,6-DMP and kcat/Km=1.611mM(-1)s(-1) for ABTS). This study has shown that three ligands that are closely associated with the T1 copper in SLAC play a key role in maintaining enzymatic activity. Whilst the introduction of mutations at these sites negated favourable characteristics such as thermostability, several favourable effects were observed. This study has also extended the knowledge base on the biochemical characteristics of SLAC, and its suitability as a template for engineering with the aim of widening its potential range of industrial applications.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Biochemical characteristics; Small laccase; T1 copper, Mutation

Mesh:

Substances:

Year:  2014        PMID: 25435502     DOI: 10.1016/j.enzmictec.2014.10.003

Source DB:  PubMed          Journal:  Enzyme Microb Technol        ISSN: 0141-0229            Impact factor:   3.493


  7 in total

Review 1.  Bacterial laccase: recent update on production, properties and industrial applications.

Authors:  Prakram Singh Chauhan; Bindi Goradia; Arunika Saxena
Journal:  3 Biotech       Date:  2017-09-16       Impact factor: 2.406

2.  Laccase: addressing the ambivalence associated with the calculation of enzyme activity.

Authors:  Komal Agrawal; Pradeep Verma
Journal:  3 Biotech       Date:  2019-09-21       Impact factor: 2.406

3.  Isolation, identification of a laccase-producing fungal strain and enzymatic properties of the laccase.

Authors:  Wen Du; Chunlong Sun; Jun Wang; Baoqin Wang; Zhigang Yao; Fanzhu Qu; Jiangbao Xia; Wenjun Xie; Jingkuan Sun; Daixiang Duan
Journal:  3 Biotech       Date:  2018-02-16       Impact factor: 2.406

4.  Substitution of the Methionine Axial Ligand of the T1 Copper for the Fungal-like Phenylalanine Ligand (M298F) Causes Local Structural Perturbations that Lead to Thermal Instability and Reduced Catalytic Efficiency of the Small Laccase from Streptomyces coelicolor A3(2).

Authors:  Kairit Zovo; Hegne Pupart; Arie Van Wieren; Richard E Gillilan; Qingqiu Huang; Sudipta Majumdar; Tiit Lukk
Journal:  ACS Omega       Date:  2022-02-09

5.  Evolving stability and pH-dependent activity of the high redox potential Botrytis aclada laccase for enzymatic fuel cells.

Authors:  Stefan Scheiblbrandner; Erik Breslmayr; Florian Csarman; Regina Paukner; Johannes Führer; Peter L Herzog; Sergey V Shleev; Evgeny M Osipov; Tamara V Tikhonova; Vladimir O Popov; Dietmar Haltrich; Roland Ludwig; Roman Kittl
Journal:  Sci Rep       Date:  2017-10-20       Impact factor: 4.379

6.  In silico Design of Laccase Thermostable Mutants From Lacc 6 of Pleurotus Ostreatus.

Authors:  Rubén Díaz; Gerardo Díaz-Godínez; Miguel Angel Anducho-Reyes; Yuridia Mercado-Flores; Leonardo David Herrera-Zúñiga
Journal:  Front Microbiol       Date:  2018-11-14       Impact factor: 5.640

7.  Broad thermal spectrum metagenomic laccase with action for dye decolorization and fentin hydroxide treatment.

Authors:  Natália Sarmanho Monteiro Lima; Elisângela Soares Gomes-Pepe; João Carlos Campanharo; Eliana Gertrudes de Macedo Lemos
Journal:  AMB Express       Date:  2022-03-23       Impact factor: 3.298

  7 in total

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