Exploring Natural Diversity of Limonene Synthases and Molecular Determinants Involved in Substrate Specificity in Escherichia coli
Limonene is a chiral, high-demand monoterpene that has wide applications in therapeutics, cosmetics, biofuels, agri-food, biomaterials, and solvent industries. However, its biosynthesis by microbial cell factories is often limited by the poor activity of limonene synthase (LS). Optimization of the r...
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Published in | Journal of agricultural and food chemistry Vol. 73; no. 22; pp. 13722 - 13735 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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21.05.2025
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Abstract | Limonene is a chiral, high-demand monoterpene that has wide applications in therapeutics, cosmetics, biofuels, agri-food, biomaterials, and solvent industries. However, its biosynthesis by microbial cell factories is often limited by the poor activity of limonene synthase (LS). Optimization of the rate-limiting enzyme is thus crucial for boosting limonene production. Here, we report the identification of ten LS homologues from sequence data mining and their testing in cells accumulating geranyl pyrophosphate (GPP) or neryl pyrophosphate (NPP) for limonene production. The selectivity of these enzymes toward GPP or NPP was investigated, leading to the identification of a limonene synthase from
that displays a clear substrate preference for NPP over GPP
. This enzyme was selected as a template for engineering. Using
analyses and mutagenesis, several mutants were engineered that revealed differences in substrate specificity. Among them, a combination of mutations (S8K/I265V/E276P/P277R/A281K/N282T/I285Q/I286L) improved limonene production by 4.8- and 1.9-fold with the GPP and NPP pathways, respectively. The mutant predominantly produced (+)-limonene from GPP and a mixture of limonene from NPP, with ∼85-90% of (+)-limonene. This decreased the selectivity for NPP by 2.4-fold. This supports the improved biological production of limonene enantiomers from renewable carbon sources. |
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AbstractList | Limonene is a chiral, high-demand monoterpene that has wide applications in therapeutics, cosmetics, biofuels, agri-food, biomaterials, and solvent industries. However, its biosynthesis by microbial cell factories is often limited by the poor activity of limonene synthase (LS). Optimization of the rate-limiting enzyme is thus crucial for boosting limonene production. Here, we report the identification of ten LS homologues from sequence data mining and their testing in cells accumulating geranyl pyrophosphate (GPP) or neryl pyrophosphate (NPP) for limonene production. The selectivity of these enzymes toward GPP or NPP was investigated, leading to the identification of a limonene synthase from Agastache rugosa that displays a clear substrate preference for NPP over GPP in vivo. This enzyme was selected as a template for engineering. Using in silico analyses and mutagenesis, several mutants were engineered that revealed differences in substrate specificity. Among them, a combination of mutations (S8K/I265V/E276P/P277R/A281K/N282T/I285Q/I286L) improved limonene production by 4.8- and 1.9-fold with the GPP and NPP pathways, respectively. The mutant predominantly produced (+)-limonene from GPP and a mixture of limonene from NPP, with ∼85-90% of (+)-limonene. This decreased the selectivity for NPP by 2.4-fold. This supports the improved biological production of limonene enantiomers from renewable carbon sources.Limonene is a chiral, high-demand monoterpene that has wide applications in therapeutics, cosmetics, biofuels, agri-food, biomaterials, and solvent industries. However, its biosynthesis by microbial cell factories is often limited by the poor activity of limonene synthase (LS). Optimization of the rate-limiting enzyme is thus crucial for boosting limonene production. Here, we report the identification of ten LS homologues from sequence data mining and their testing in cells accumulating geranyl pyrophosphate (GPP) or neryl pyrophosphate (NPP) for limonene production. The selectivity of these enzymes toward GPP or NPP was investigated, leading to the identification of a limonene synthase from Agastache rugosa that displays a clear substrate preference for NPP over GPP in vivo. This enzyme was selected as a template for engineering. Using in silico analyses and mutagenesis, several mutants were engineered that revealed differences in substrate specificity. Among them, a combination of mutations (S8K/I265V/E276P/P277R/A281K/N282T/I285Q/I286L) improved limonene production by 4.8- and 1.9-fold with the GPP and NPP pathways, respectively. The mutant predominantly produced (+)-limonene from GPP and a mixture of limonene from NPP, with ∼85-90% of (+)-limonene. This decreased the selectivity for NPP by 2.4-fold. This supports the improved biological production of limonene enantiomers from renewable carbon sources. Limonene is a chiral, high-demand monoterpene that has wide applications in therapeutics, cosmetics, biofuels, agri-food, biomaterials, and solvent industries. However, its biosynthesis by microbial cell factories is often limited by the poor activity of limonene synthase (LS). Optimization of the rate-limiting enzyme is thus crucial for boosting limonene production. Here, we report the identification of ten LS homologues from sequence data mining and their testing in cells accumulating geranyl pyrophosphate (GPP) or neryl pyrophosphate (NPP) for limonene production. The selectivity of these enzymes toward GPP or NPP was investigated, leading to the identification of a limonene synthase from that displays a clear substrate preference for NPP over GPP . This enzyme was selected as a template for engineering. Using analyses and mutagenesis, several mutants were engineered that revealed differences in substrate specificity. Among them, a combination of mutations (S8K/I265V/E276P/P277R/A281K/N282T/I285Q/I286L) improved limonene production by 4.8- and 1.9-fold with the GPP and NPP pathways, respectively. The mutant predominantly produced (+)-limonene from GPP and a mixture of limonene from NPP, with ∼85-90% of (+)-limonene. This decreased the selectivity for NPP by 2.4-fold. This supports the improved biological production of limonene enantiomers from renewable carbon sources. Limonene is a chiral, high-demand monoterpene that has wide applications in therapeutics, cosmetics, biofuels, agri-food, biomaterials, and solvent industries. However, its biosynthesis by microbial cell factories is often limited by the poor activity of limonene synthase (LS). Optimization of the rate-limiting enzyme is thus crucial for boosting limonene production. Here, we report the identification of ten LS homologues from sequence data mining and their testing in cells accumulating geranyl pyrophosphate (GPP) or neryl pyrophosphate (NPP) for limonene production. The selectivity of these enzymes toward GPP or NPP was investigated, leading to the identification of a limonene synthase from Agastache rugosa that displays a clear substrate preference for NPP over GPP in vivo. This enzyme was selected as a template for engineering. Using in silico analyses and mutagenesis, several mutants were engineered that revealed differences in substrate specificity. Among them, a combination of mutations (S8K/I265V/E276P/P277R/A281K/N282T/I285Q/I286L) improved limonene production by 4.8- and 1.9-fold with the GPP and NPP pathways, respectively. The mutant predominantly produced (+)-limonene from GPP and a mixture of limonene from NPP, with ∼85–90% of (+)-limonene. This decreased the selectivity for NPP by 2.4-fold. This supports the improved biological production of limonene enantiomers from renewable carbon sources. |
Author | André, Isabelle Bozonnet, Sophie Esque, Jérémy Borkar, Shreyash Xue, Bo Scipion, Clement P. M. Remaud-Siméon, Magali Yew, Wen Shan Chen, Xixian Seah, Cristalle |
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Cites_doi | 10.1002/marc.202200185 10.1021/acs.biochem.7b00143 10.1021/bi980854k 10.1021/acs.jctc.1c00645 10.1016/j.abb.2017.12.007 10.1039/C8GC02957A 10.1073/pnas.1501203112 10.1002/open.201900015 10.1371/journal.pone.0056769 10.1126/science.1225829 10.3389/fpls.2022.850130 10.1073/pnas.0904113106 10.1073/pnas.0700915104 10.1021/acs.jafc.9b01427 10.1016/j.algal.2016.10.020 10.1007/s00253-019-09892-y 10.1021/acssynbio.9b00135 10.1016/j.cbi.2018.02.007 10.1007/s00253-024-13273-5 10.3390/molecules26154535 10.1093/genetics/158.2.811 10.1016/j.phytochem.2017.02.017 10.1038/s41467-022-35232-2 10.1039/D1SC03741B 10.1039/D2RA08182B 10.1039/C4CC06147K 10.1073/pnas.95.8.4126 10.1046/j.1432-1033.2002.02985.x 10.3390/molecules25081881 10.1006/abbi.1999.1332 10.1021/jf900652a 10.1038/s41586-021-03819-2 10.1002/fsn3.1372 10.1016/j.ymben.2014.11.011 10.1093/bioinformatics/bts565 10.1104/pp.105.071803 10.1038/s41467-019-11290-x 10.1186/s13068-021-01998-8 10.1021/acs.jchemed.1c00363 10.1002/bbb.1677 10.1016/j.phytochem.2013.01.005 10.1002/jcc.20291 10.1016/j.fct.2018.07.052 10.1186/s12934-022-01746-z 10.3390/molecules25112598 10.1248/bpb.25.661 10.1038/nmeth.4067 10.1248/bpb.24.373 10.1016/j.procbio.2011.05.012 10.1002/bit.26296 10.1016/j.abb.2007.06.011 10.1021/acscatal.8b00692 10.1021/acs.biochem.7b00144 10.1007/s00253-016-7337-7 10.1093/bib/bbx108 10.1016/j.jsb.2010.06.016 10.1093/bioinformatics/btl158 10.1371/journal.pone.0173911 10.1016/j.ymben.2013.05.004 10.1093/nar/gkaa913 10.1177/1934578X0700200301 10.1093/nar/gku316 10.1038/s41589-018-0166-5 10.1002/bit.20128 |
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Keywords | enantioselectivity limonene enzyme engineering monoterpene neryl pyrophosphate terpenoid Agastache rugosa geranyl pyrophosphate limonene synthase |
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SubjectTerms | Agastache rugosa biocompatible materials biofuels biological production biosynthesis carbon computer simulation cosmetics enantiomers enzymes Escherichia coli food chemistry limonene mutagenesis mutants solvents substrate specificity therapeutics |
Title | Exploring Natural Diversity of Limonene Synthases and Molecular Determinants Involved in Substrate Specificity in Escherichia coli |
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