Molecular cloning and expression analysis of mevalonate pyrophosphate decarboxylase in Antrodia cinnamomea

Mevalonate pyrophosphate decarboxylase (MVD) plays important roles in triterpenoid biosynthesis via the mevalonate pathway. A novel MVD gene was isolated and identified in Antrodia cinnamomea (Ac-mvd). The full-length cDNA contained an open reading frame with a length of 1,209 bp and encoded a 402-a...

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Main Authors: Li Jing, Lin Xiong-Jie, Shao En-Si, Lin Zhan-Xi
Format: Article
Language:English
Published: EDP Sciences 2016-01-01
Series:MATEC Web of Conferences
Online Access:http://dx.doi.org/10.1051/matecconf/20166403001
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spelling doaj-6a42773e3ddf4002964e346651cd90fc2021-02-02T04:23:44ZengEDP SciencesMATEC Web of Conferences2261-236X2016-01-01640300110.1051/matecconf/20166403001matecconf_iccmp2016_03001Molecular cloning and expression analysis of mevalonate pyrophosphate decarboxylase in Antrodia cinnamomeaLi JingLin Xiong-Jie0Shao En-SiLin Zhan-XiFruit Research Institute, Fujian Academy of Agriculture SciencesMevalonate pyrophosphate decarboxylase (MVD) plays important roles in triterpenoid biosynthesis via the mevalonate pathway. A novel MVD gene was isolated and identified in Antrodia cinnamomea (Ac-mvd). The full-length cDNA contained an open reading frame with a length of 1,209 bp and encoded a 402-amino acid polypeptide with a molecular mass of 43.3 kDa and a theoretical pI of 8.23. As incubation time was prolonged for 28 days, the triterpenoid content in the mycelium gradually increased and reached 39.192 ± 2.025 mg/g; the triterpenoid content of the fruiting body grew in the hay of Cinnamomum kanehirae (ACFB-CK), was 49.391 ± 2.675 mg/g, which was significantly different from other samples (P < 0.05). qRT-PCR revealed that the highest expression levels of Ac-mvd in the mycelium of Antrodia cinnamomea were detected on the 7th day. The expression levels gradually decreased as culture time was extended from 14 days to 42 days.http://dx.doi.org/10.1051/matecconf/20166403001
collection DOAJ
language English
format Article
sources DOAJ
author Li Jing
Lin Xiong-Jie
Shao En-Si
Lin Zhan-Xi
spellingShingle Li Jing
Lin Xiong-Jie
Shao En-Si
Lin Zhan-Xi
Molecular cloning and expression analysis of mevalonate pyrophosphate decarboxylase in Antrodia cinnamomea
MATEC Web of Conferences
author_facet Li Jing
Lin Xiong-Jie
Shao En-Si
Lin Zhan-Xi
author_sort Li Jing
title Molecular cloning and expression analysis of mevalonate pyrophosphate decarboxylase in Antrodia cinnamomea
title_short Molecular cloning and expression analysis of mevalonate pyrophosphate decarboxylase in Antrodia cinnamomea
title_full Molecular cloning and expression analysis of mevalonate pyrophosphate decarboxylase in Antrodia cinnamomea
title_fullStr Molecular cloning and expression analysis of mevalonate pyrophosphate decarboxylase in Antrodia cinnamomea
title_full_unstemmed Molecular cloning and expression analysis of mevalonate pyrophosphate decarboxylase in Antrodia cinnamomea
title_sort molecular cloning and expression analysis of mevalonate pyrophosphate decarboxylase in antrodia cinnamomea
publisher EDP Sciences
series MATEC Web of Conferences
issn 2261-236X
publishDate 2016-01-01
description Mevalonate pyrophosphate decarboxylase (MVD) plays important roles in triterpenoid biosynthesis via the mevalonate pathway. A novel MVD gene was isolated and identified in Antrodia cinnamomea (Ac-mvd). The full-length cDNA contained an open reading frame with a length of 1,209 bp and encoded a 402-amino acid polypeptide with a molecular mass of 43.3 kDa and a theoretical pI of 8.23. As incubation time was prolonged for 28 days, the triterpenoid content in the mycelium gradually increased and reached 39.192 ± 2.025 mg/g; the triterpenoid content of the fruiting body grew in the hay of Cinnamomum kanehirae (ACFB-CK), was 49.391 ± 2.675 mg/g, which was significantly different from other samples (P < 0.05). qRT-PCR revealed that the highest expression levels of Ac-mvd in the mycelium of Antrodia cinnamomea were detected on the 7th day. The expression levels gradually decreased as culture time was extended from 14 days to 42 days.
url http://dx.doi.org/10.1051/matecconf/20166403001
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