Cargando…
Two unexpected promiscuous activities of the iron–sulfur protein IspH in production of isoprene and isoamylene
BACKGROUND: Bacillus species, possessing the methylerythritol phosphate (MEP) pathway for the synthesis of isoprenoid feedstock, are the highest producers of isoprene among bacteria; however, the enzyme responsible for isoprene synthesis has not been identified. The iron–sulfur protein IspH is the f...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4864966/ https://www.ncbi.nlm.nih.gov/pubmed/27169371 http://dx.doi.org/10.1186/s12934-016-0476-9 |
_version_ | 1782431709968465920 |
---|---|
author | Ge, Deyong Xue, Yanfen Ma, Yanhe |
author_facet | Ge, Deyong Xue, Yanfen Ma, Yanhe |
author_sort | Ge, Deyong |
collection | PubMed |
description | BACKGROUND: Bacillus species, possessing the methylerythritol phosphate (MEP) pathway for the synthesis of isoprenoid feedstock, are the highest producers of isoprene among bacteria; however, the enzyme responsible for isoprene synthesis has not been identified. The iron–sulfur protein IspH is the final enzyme of the MEP pathway and catalyses the reductive dehydration of (E)-4-hydroxy-3-methyl-2-butenyl diphosphate (HMBPP) to form isopentenyl diphosphate and dimethylallyl diphosphate (DMAPP). In this study, we demonstrated two unexpected promiscuous activities of IspH from alkaliphilic Bacillus sp. N16-5, which can produce high levels of isoprene. RESULTS: Bacillus sp. N16-5 IspH could catalyse the formation of isoprene from HMBPP and the conversion of DMAPP into a mixture of 2-methyl-2-butene and 3-methyl-1-butene. Both reactions require an electron transfer system, such as that used for HMBPP dehydration. Isoprene and isoamylene synthesis in Bacillus sp. N16-5 was investigated and the reaction system was reconstituted in vitro, including IspH, ferredoxin and ferredoxin-NADP(+)-reductase proteins and NADPH. The roles of specific IspH protein residues were also investigated by site-directed mutagenesis experiments; two variants (H131N and E133Q) were found to have lost the HMBPP reductase activity but could still catalyse the formation of isoprene. Overexpression of IspH H131N in Bacillus sp. N16-5 resulted in a twofold enhancement of isoprene production, and the yield of isoprene from the strain expressing E133Q was increased 300 % compared with the wild-type strain. CONCLUSIONS: IspH from Bacillus sp. N16-5 is a promiscuous enzyme that can catalyse formation of isoprene and isoamylene. This enzyme, especially the H131N and E133Q variants, could be used for the production of isoprene from HMBPP. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-016-0476-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4864966 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48649662016-05-13 Two unexpected promiscuous activities of the iron–sulfur protein IspH in production of isoprene and isoamylene Ge, Deyong Xue, Yanfen Ma, Yanhe Microb Cell Fact Research BACKGROUND: Bacillus species, possessing the methylerythritol phosphate (MEP) pathway for the synthesis of isoprenoid feedstock, are the highest producers of isoprene among bacteria; however, the enzyme responsible for isoprene synthesis has not been identified. The iron–sulfur protein IspH is the final enzyme of the MEP pathway and catalyses the reductive dehydration of (E)-4-hydroxy-3-methyl-2-butenyl diphosphate (HMBPP) to form isopentenyl diphosphate and dimethylallyl diphosphate (DMAPP). In this study, we demonstrated two unexpected promiscuous activities of IspH from alkaliphilic Bacillus sp. N16-5, which can produce high levels of isoprene. RESULTS: Bacillus sp. N16-5 IspH could catalyse the formation of isoprene from HMBPP and the conversion of DMAPP into a mixture of 2-methyl-2-butene and 3-methyl-1-butene. Both reactions require an electron transfer system, such as that used for HMBPP dehydration. Isoprene and isoamylene synthesis in Bacillus sp. N16-5 was investigated and the reaction system was reconstituted in vitro, including IspH, ferredoxin and ferredoxin-NADP(+)-reductase proteins and NADPH. The roles of specific IspH protein residues were also investigated by site-directed mutagenesis experiments; two variants (H131N and E133Q) were found to have lost the HMBPP reductase activity but could still catalyse the formation of isoprene. Overexpression of IspH H131N in Bacillus sp. N16-5 resulted in a twofold enhancement of isoprene production, and the yield of isoprene from the strain expressing E133Q was increased 300 % compared with the wild-type strain. CONCLUSIONS: IspH from Bacillus sp. N16-5 is a promiscuous enzyme that can catalyse formation of isoprene and isoamylene. This enzyme, especially the H131N and E133Q variants, could be used for the production of isoprene from HMBPP. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-016-0476-9) contains supplementary material, which is available to authorized users. BioMed Central 2016-05-11 /pmc/articles/PMC4864966/ /pubmed/27169371 http://dx.doi.org/10.1186/s12934-016-0476-9 Text en © Ge et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Ge, Deyong Xue, Yanfen Ma, Yanhe Two unexpected promiscuous activities of the iron–sulfur protein IspH in production of isoprene and isoamylene |
title | Two unexpected promiscuous activities of the iron–sulfur protein IspH in production of isoprene and isoamylene |
title_full | Two unexpected promiscuous activities of the iron–sulfur protein IspH in production of isoprene and isoamylene |
title_fullStr | Two unexpected promiscuous activities of the iron–sulfur protein IspH in production of isoprene and isoamylene |
title_full_unstemmed | Two unexpected promiscuous activities of the iron–sulfur protein IspH in production of isoprene and isoamylene |
title_short | Two unexpected promiscuous activities of the iron–sulfur protein IspH in production of isoprene and isoamylene |
title_sort | two unexpected promiscuous activities of the iron–sulfur protein isph in production of isoprene and isoamylene |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4864966/ https://www.ncbi.nlm.nih.gov/pubmed/27169371 http://dx.doi.org/10.1186/s12934-016-0476-9 |
work_keys_str_mv | AT gedeyong twounexpectedpromiscuousactivitiesoftheironsulfurproteinisphinproductionofisopreneandisoamylene AT xueyanfen twounexpectedpromiscuousactivitiesoftheironsulfurproteinisphinproductionofisopreneandisoamylene AT mayanhe twounexpectedpromiscuousactivitiesoftheironsulfurproteinisphinproductionofisopreneandisoamylene |