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Functional characterization of a new terpene synthase from Plectranthus amboinicus

Plectranthus amboinicus (Lour.) Spreng is an aromatic medicinal herb known for its therapeutic and nutritional properties attributed by the presence of monoterpene and sesquiterpene compounds. Up until now, research on terpenoid biosynthesis has focused on a few mint species with economic importance...

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Autores principales: Ashaari, Nur Suhanawati, Ab. Rahim, Mohd Hairul, Sabri, Suriana, Lai, Kok Song, Song, Adelene Ai-Lian, Abdul Rahim, Raha, Wan Abdullah, Wan Muhamad Asrul Nizam, Ong Abdullah, Janna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7332032/
https://www.ncbi.nlm.nih.gov/pubmed/32614884
http://dx.doi.org/10.1371/journal.pone.0235416
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author Ashaari, Nur Suhanawati
Ab. Rahim, Mohd Hairul
Sabri, Suriana
Lai, Kok Song
Song, Adelene Ai-Lian
Abdul Rahim, Raha
Wan Abdullah, Wan Muhamad Asrul Nizam
Ong Abdullah, Janna
author_facet Ashaari, Nur Suhanawati
Ab. Rahim, Mohd Hairul
Sabri, Suriana
Lai, Kok Song
Song, Adelene Ai-Lian
Abdul Rahim, Raha
Wan Abdullah, Wan Muhamad Asrul Nizam
Ong Abdullah, Janna
author_sort Ashaari, Nur Suhanawati
collection PubMed
description Plectranthus amboinicus (Lour.) Spreng is an aromatic medicinal herb known for its therapeutic and nutritional properties attributed by the presence of monoterpene and sesquiterpene compounds. Up until now, research on terpenoid biosynthesis has focused on a few mint species with economic importance such as thyme and oregano, yet the terpene synthases responsible for monoterpene production in P. amboinicus have not been described. Here we report the isolation, heterologous expression and functional characterization of a terpene synthase involved in P. amboinicus terpenoid biosynthesis. A putative monoterpene synthase gene (PamTps1) from P. amboinicus was isolated with an open reading frame of 1797 bp encoding a predicted protein of 598 amino acids with molecular weight of 69.6 kDa. PamTps1 shares 60–70% amino acid sequence similarity with other known terpene synthases of Lamiaceae. The in vitro enzymatic activity of PamTps1 demonstrated the conversion of geranyl pyrophosphate and farnesyl pyrophosphate exclusively into linalool and nerolidol, respectively, and thus PamTps1 was classified as a linalool/nerolidol synthase. In vivo activity of PamTps1 in a recombinant Escherichia coli strain revealed production of linalool and nerolidol which correlated with its in vitro activity. This outcome validated the multi-substrate usage of this enzyme in producing linalool and nerolidol both in in vivo and in vitro systems. The transcript level of PamTps1 was prominent in the leaf during daytime as compared to the stem. Gas chromatography-mass spectrometry (GC-MS) and quantitative real-time PCR analyses showed that maximal linalool level was released during the daytime and lower at night following a diurnal circadian pattern which correlated with the PamTps1 expression pattern. The PamTps1 cloned herein provides a molecular basis for the terpenoid biosynthesis in this local herb that could be exploited for valuable production using metabolic engineering in both microbial and plant systems.
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spelling pubmed-73320322020-07-15 Functional characterization of a new terpene synthase from Plectranthus amboinicus Ashaari, Nur Suhanawati Ab. Rahim, Mohd Hairul Sabri, Suriana Lai, Kok Song Song, Adelene Ai-Lian Abdul Rahim, Raha Wan Abdullah, Wan Muhamad Asrul Nizam Ong Abdullah, Janna PLoS One Research Article Plectranthus amboinicus (Lour.) Spreng is an aromatic medicinal herb known for its therapeutic and nutritional properties attributed by the presence of monoterpene and sesquiterpene compounds. Up until now, research on terpenoid biosynthesis has focused on a few mint species with economic importance such as thyme and oregano, yet the terpene synthases responsible for monoterpene production in P. amboinicus have not been described. Here we report the isolation, heterologous expression and functional characterization of a terpene synthase involved in P. amboinicus terpenoid biosynthesis. A putative monoterpene synthase gene (PamTps1) from P. amboinicus was isolated with an open reading frame of 1797 bp encoding a predicted protein of 598 amino acids with molecular weight of 69.6 kDa. PamTps1 shares 60–70% amino acid sequence similarity with other known terpene synthases of Lamiaceae. The in vitro enzymatic activity of PamTps1 demonstrated the conversion of geranyl pyrophosphate and farnesyl pyrophosphate exclusively into linalool and nerolidol, respectively, and thus PamTps1 was classified as a linalool/nerolidol synthase. In vivo activity of PamTps1 in a recombinant Escherichia coli strain revealed production of linalool and nerolidol which correlated with its in vitro activity. This outcome validated the multi-substrate usage of this enzyme in producing linalool and nerolidol both in in vivo and in vitro systems. The transcript level of PamTps1 was prominent in the leaf during daytime as compared to the stem. Gas chromatography-mass spectrometry (GC-MS) and quantitative real-time PCR analyses showed that maximal linalool level was released during the daytime and lower at night following a diurnal circadian pattern which correlated with the PamTps1 expression pattern. The PamTps1 cloned herein provides a molecular basis for the terpenoid biosynthesis in this local herb that could be exploited for valuable production using metabolic engineering in both microbial and plant systems. Public Library of Science 2020-07-02 /pmc/articles/PMC7332032/ /pubmed/32614884 http://dx.doi.org/10.1371/journal.pone.0235416 Text en © 2020 Ashaari et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ashaari, Nur Suhanawati
Ab. Rahim, Mohd Hairul
Sabri, Suriana
Lai, Kok Song
Song, Adelene Ai-Lian
Abdul Rahim, Raha
Wan Abdullah, Wan Muhamad Asrul Nizam
Ong Abdullah, Janna
Functional characterization of a new terpene synthase from Plectranthus amboinicus
title Functional characterization of a new terpene synthase from Plectranthus amboinicus
title_full Functional characterization of a new terpene synthase from Plectranthus amboinicus
title_fullStr Functional characterization of a new terpene synthase from Plectranthus amboinicus
title_full_unstemmed Functional characterization of a new terpene synthase from Plectranthus amboinicus
title_short Functional characterization of a new terpene synthase from Plectranthus amboinicus
title_sort functional characterization of a new terpene synthase from plectranthus amboinicus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7332032/
https://www.ncbi.nlm.nih.gov/pubmed/32614884
http://dx.doi.org/10.1371/journal.pone.0235416
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