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Cloning, expression and application of a novel laccase derived from water buffalo ruminal lignin-degrading bacteria.
- Source :
-
International journal of biological macromolecules [Int J Biol Macromol] 2024 May; Vol. 266 (Pt 2), pp. 131109. Date of Electronic Publication: 2024 Mar 24. - Publication Year :
- 2024
-
Abstract
- Water buffalo is the only mammal found to degrade lignin so far, and laccase plays an indispensable role in the degradation of lignin. In this study, multiple laccase genes were amplified based on the water buffalo rumen derived lignin-degrading bacteria Bacillus cereus and Ochrobactrum pseudintermedium. Subsequently, the corresponding recombinant plasmids were transformed into E. coli expression system BL21 (DE3) for induced expression by Isopropyl-β-D-thiogalactopyranoside (IPTG). After preliminary screening, protein purification and enzyme activity assays, Lac3833 with soluble expression and high enzyme activity was selected to test its characteristics, especially the ability of lignin degradation. The results showed that the optimum reaction temperature of Lac3833 was 40 °C for different substrates. The relative activity of Lac3833 reached the highest at pH 4.5 and pH 5.5 when the substrates were ABTS or 2,6-DMP and guaiacol, respectively. Additionally, Lac3833 could maintain high enzyme activity in different temperatures, pH and solutions containing Na <superscript>+</superscript> , K <superscript>+</superscript> , Mg <superscript>2+</superscript> , Ca <superscript>2+</superscript> and Mn <superscript>2+</superscript> . Importantly, compared to negative treatment, recombinant laccase Lac3833 treatment showed that it had a significant function in degrading lignin. In conclusion, this is a pioneering study to produce recombinant laccase with lignin-degrading ability by bacteria from water buffalo rumen, which will provide new insights for the exploitation of more lignin-degrading enzymes.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Hydrogen-Ion Concentration
Gene Expression
Escherichia coli genetics
Escherichia coli metabolism
Bacteria enzymology
Bacteria genetics
Substrate Specificity
Laccase genetics
Laccase metabolism
Lignin metabolism
Buffaloes
Cloning, Molecular
Rumen microbiology
Recombinant Proteins metabolism
Recombinant Proteins genetics
Temperature
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0003
- Volume :
- 266
- Issue :
- Pt 2
- Database :
- MEDLINE
- Journal :
- International journal of biological macromolecules
- Publication Type :
- Academic Journal
- Accession number :
- 38531520
- Full Text :
- https://doi.org/10.1016/j.ijbiomac.2024.131109