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Expression of novel acidic lipase from Micrococcus luteus in Pichia pastoris and its application in transesterification
BACKGROUND: Lipases are promising biocatalysts for industrial applications and attract attention to be explored. A novel acidic lipase has been isolated from the lipolytic bacteria Micrococcus luteus EMP48-D (LipEMP48-D) screened from tempeh. The lipase gene had previously been overexpressed in Esch...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8026790/ https://www.ncbi.nlm.nih.gov/pubmed/33826047 http://dx.doi.org/10.1186/s43141-021-00155-w |
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author | Adina, Selfela Restu Suwanto, Antonius Meryandini, Anja Puspitasari, Esti |
author_facet | Adina, Selfela Restu Suwanto, Antonius Meryandini, Anja Puspitasari, Esti |
author_sort | Adina, Selfela Restu |
collection | PubMed |
description | BACKGROUND: Lipases are promising biocatalysts for industrial applications and attract attention to be explored. A novel acidic lipase has been isolated from the lipolytic bacteria Micrococcus luteus EMP48-D (LipEMP48-D) screened from tempeh. The lipase gene had previously been overexpressed in Escherichia coli BL21, but the expression level obtained was relatively low. Here, to improve the expression level, the lipase gene was cloned to Pichia pastoris. We eliminated the native signal sequence of M. luteus and replaced it with α-mating factor (α-MF) signal sequence. We also optimized and synthesized the lipase gene based on codon preference in P. pastoris. RESULTS: LipEMP48-D lipase was expressed as an extracellular protein. Codon optimization has been conducted for 20 codons, with the codon adaption index reaching 0.995. The highest extracellular lipase activity obtained reached 145.4 ± 4.8 U/mg under AOX1 promoter in P. pastoris KM71 strain, which was 9.7-fold higher than the previous activity in E. coli. LipEMP48-D showed the highest specific activity at pH 5.0 and stable within the pH range 3.0–5.0 at 40 °C. LipEMP48-D also has the capability of hydrolyzing various long-chain triglycerides, particularly olive oil (100%) followed by sunflower oil (88.5%). LipEMP48-D exhibited high tolerance for various polar organic solvents with low log P, such as isopropanol (115.7%) and butanol (114.6%). The metal ions (Na(+), K(+), Ca(2+), Mg(2+), Mn(+)) decreased enzyme activity up to 43.1%, while Fe(2+) increased relative activity of enzymes up to 200%. The conversion of free fatty acid (FFA) into fatty acid methyl ester (FAME) was low around 2.95%. CONCLUSIONS: This study was the first to report overexpression of Micrococcus lipase in yeast. The extracellular expression of this acidic lipase could be potential for biocatalyst in industrial fields, especially organic synthesis, food industry, and production of biodiesel. |
format | Online Article Text |
id | pubmed-8026790 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-80267902021-04-12 Expression of novel acidic lipase from Micrococcus luteus in Pichia pastoris and its application in transesterification Adina, Selfela Restu Suwanto, Antonius Meryandini, Anja Puspitasari, Esti J Genet Eng Biotechnol Research BACKGROUND: Lipases are promising biocatalysts for industrial applications and attract attention to be explored. A novel acidic lipase has been isolated from the lipolytic bacteria Micrococcus luteus EMP48-D (LipEMP48-D) screened from tempeh. The lipase gene had previously been overexpressed in Escherichia coli BL21, but the expression level obtained was relatively low. Here, to improve the expression level, the lipase gene was cloned to Pichia pastoris. We eliminated the native signal sequence of M. luteus and replaced it with α-mating factor (α-MF) signal sequence. We also optimized and synthesized the lipase gene based on codon preference in P. pastoris. RESULTS: LipEMP48-D lipase was expressed as an extracellular protein. Codon optimization has been conducted for 20 codons, with the codon adaption index reaching 0.995. The highest extracellular lipase activity obtained reached 145.4 ± 4.8 U/mg under AOX1 promoter in P. pastoris KM71 strain, which was 9.7-fold higher than the previous activity in E. coli. LipEMP48-D showed the highest specific activity at pH 5.0 and stable within the pH range 3.0–5.0 at 40 °C. LipEMP48-D also has the capability of hydrolyzing various long-chain triglycerides, particularly olive oil (100%) followed by sunflower oil (88.5%). LipEMP48-D exhibited high tolerance for various polar organic solvents with low log P, such as isopropanol (115.7%) and butanol (114.6%). The metal ions (Na(+), K(+), Ca(2+), Mg(2+), Mn(+)) decreased enzyme activity up to 43.1%, while Fe(2+) increased relative activity of enzymes up to 200%. The conversion of free fatty acid (FFA) into fatty acid methyl ester (FAME) was low around 2.95%. CONCLUSIONS: This study was the first to report overexpression of Micrococcus lipase in yeast. The extracellular expression of this acidic lipase could be potential for biocatalyst in industrial fields, especially organic synthesis, food industry, and production of biodiesel. Springer Berlin Heidelberg 2021-04-07 /pmc/articles/PMC8026790/ /pubmed/33826047 http://dx.doi.org/10.1186/s43141-021-00155-w Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Adina, Selfela Restu Suwanto, Antonius Meryandini, Anja Puspitasari, Esti Expression of novel acidic lipase from Micrococcus luteus in Pichia pastoris and its application in transesterification |
title | Expression of novel acidic lipase from Micrococcus luteus in Pichia pastoris and its application in transesterification |
title_full | Expression of novel acidic lipase from Micrococcus luteus in Pichia pastoris and its application in transesterification |
title_fullStr | Expression of novel acidic lipase from Micrococcus luteus in Pichia pastoris and its application in transesterification |
title_full_unstemmed | Expression of novel acidic lipase from Micrococcus luteus in Pichia pastoris and its application in transesterification |
title_short | Expression of novel acidic lipase from Micrococcus luteus in Pichia pastoris and its application in transesterification |
title_sort | expression of novel acidic lipase from micrococcus luteus in pichia pastoris and its application in transesterification |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8026790/ https://www.ncbi.nlm.nih.gov/pubmed/33826047 http://dx.doi.org/10.1186/s43141-021-00155-w |
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