Cargando…
From linoleic acid to hexanal and hexanol by whole cell catalysis with a lipoxygenase, hydroperoxide lyase and reductase cascade in Komagataella phaffii
Green leaf volatiles (GLVs) cover a group of mainly C6-and C9-aldehydes, -alcohols and -esters. Their name refers to their characteristic herbal and fruity scent, which is similar to that of freshly cut grass or vegetables. Lipoxygenases (LOXs) catalyze the peroxidation of unsaturated fatty acids. T...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9791951/ https://www.ncbi.nlm.nih.gov/pubmed/36579187 http://dx.doi.org/10.3389/fmolb.2022.965315 |
_version_ | 1784859528451325952 |
---|---|
author | Hashem, Chiam Hochrinner, Julius Bürgler, Moritz B. Rinnofner, Claudia Pichler, Harald Winkler, Margit |
author_facet | Hashem, Chiam Hochrinner, Julius Bürgler, Moritz B. Rinnofner, Claudia Pichler, Harald Winkler, Margit |
author_sort | Hashem, Chiam |
collection | PubMed |
description | Green leaf volatiles (GLVs) cover a group of mainly C6-and C9-aldehydes, -alcohols and -esters. Their name refers to their characteristic herbal and fruity scent, which is similar to that of freshly cut grass or vegetables. Lipoxygenases (LOXs) catalyze the peroxidation of unsaturated fatty acids. The resulting hydroperoxy fatty acids are then cleaved into aldehydes and oxo acids by fatty acid hydroperoxide lyases (HPLs). Herein, we equipped the yeast Komagataella phaffii with recombinant genes coding for LOX and HPL, to serve as a biocatalyst for GLV production. We expressed the well-known 13S-specific LOX gene from Pleurotus sapidus and a compatible HPL gene from Medicago truncatula. In bioconversions, glycerol induced strains formed 12.9 mM hexanal using whole cells, and 8 mM hexanol was produced with whole cells induced by methanol. We applied various inducible and constitutive promoters in bidirectional systems to influence the final ratio of LOX and HPL proteins. By implementing these recombinant enzymes in Komagataella phaffii, challenges such as biocatalyst supply and lack of product specificity can finally be overcome. |
format | Online Article Text |
id | pubmed-9791951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97919512022-12-27 From linoleic acid to hexanal and hexanol by whole cell catalysis with a lipoxygenase, hydroperoxide lyase and reductase cascade in Komagataella phaffii Hashem, Chiam Hochrinner, Julius Bürgler, Moritz B. Rinnofner, Claudia Pichler, Harald Winkler, Margit Front Mol Biosci Molecular Biosciences Green leaf volatiles (GLVs) cover a group of mainly C6-and C9-aldehydes, -alcohols and -esters. Their name refers to their characteristic herbal and fruity scent, which is similar to that of freshly cut grass or vegetables. Lipoxygenases (LOXs) catalyze the peroxidation of unsaturated fatty acids. The resulting hydroperoxy fatty acids are then cleaved into aldehydes and oxo acids by fatty acid hydroperoxide lyases (HPLs). Herein, we equipped the yeast Komagataella phaffii with recombinant genes coding for LOX and HPL, to serve as a biocatalyst for GLV production. We expressed the well-known 13S-specific LOX gene from Pleurotus sapidus and a compatible HPL gene from Medicago truncatula. In bioconversions, glycerol induced strains formed 12.9 mM hexanal using whole cells, and 8 mM hexanol was produced with whole cells induced by methanol. We applied various inducible and constitutive promoters in bidirectional systems to influence the final ratio of LOX and HPL proteins. By implementing these recombinant enzymes in Komagataella phaffii, challenges such as biocatalyst supply and lack of product specificity can finally be overcome. Frontiers Media S.A. 2022-12-12 /pmc/articles/PMC9791951/ /pubmed/36579187 http://dx.doi.org/10.3389/fmolb.2022.965315 Text en Copyright © 2022 Hashem, Hochrinner, Bürgler, Rinnofner, Pichler and Winkler. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Molecular Biosciences Hashem, Chiam Hochrinner, Julius Bürgler, Moritz B. Rinnofner, Claudia Pichler, Harald Winkler, Margit From linoleic acid to hexanal and hexanol by whole cell catalysis with a lipoxygenase, hydroperoxide lyase and reductase cascade in Komagataella phaffii |
title | From linoleic acid to hexanal and hexanol by whole cell catalysis with a lipoxygenase, hydroperoxide lyase and reductase cascade in Komagataella phaffii
|
title_full | From linoleic acid to hexanal and hexanol by whole cell catalysis with a lipoxygenase, hydroperoxide lyase and reductase cascade in Komagataella phaffii
|
title_fullStr | From linoleic acid to hexanal and hexanol by whole cell catalysis with a lipoxygenase, hydroperoxide lyase and reductase cascade in Komagataella phaffii
|
title_full_unstemmed | From linoleic acid to hexanal and hexanol by whole cell catalysis with a lipoxygenase, hydroperoxide lyase and reductase cascade in Komagataella phaffii
|
title_short | From linoleic acid to hexanal and hexanol by whole cell catalysis with a lipoxygenase, hydroperoxide lyase and reductase cascade in Komagataella phaffii
|
title_sort | from linoleic acid to hexanal and hexanol by whole cell catalysis with a lipoxygenase, hydroperoxide lyase and reductase cascade in komagataella phaffii |
topic | Molecular Biosciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9791951/ https://www.ncbi.nlm.nih.gov/pubmed/36579187 http://dx.doi.org/10.3389/fmolb.2022.965315 |
work_keys_str_mv | AT hashemchiam fromlinoleicacidtohexanalandhexanolbywholecellcatalysiswithalipoxygenasehydroperoxidelyaseandreductasecascadeinkomagataellaphaffii AT hochrinnerjulius fromlinoleicacidtohexanalandhexanolbywholecellcatalysiswithalipoxygenasehydroperoxidelyaseandreductasecascadeinkomagataellaphaffii AT burglermoritzb fromlinoleicacidtohexanalandhexanolbywholecellcatalysiswithalipoxygenasehydroperoxidelyaseandreductasecascadeinkomagataellaphaffii AT rinnofnerclaudia fromlinoleicacidtohexanalandhexanolbywholecellcatalysiswithalipoxygenasehydroperoxidelyaseandreductasecascadeinkomagataellaphaffii AT pichlerharald fromlinoleicacidtohexanalandhexanolbywholecellcatalysiswithalipoxygenasehydroperoxidelyaseandreductasecascadeinkomagataellaphaffii AT winklermargit fromlinoleicacidtohexanalandhexanolbywholecellcatalysiswithalipoxygenasehydroperoxidelyaseandreductasecascadeinkomagataellaphaffii |