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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...

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Autores principales: Adina, Selfela Restu, Suwanto, Antonius, Meryandini, Anja, Puspitasari, Esti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
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.
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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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