Cloning, molecular properties and differential expression analysis of the isopentenyl diphosphate isomerase gene in Sanghuangporus baumii

Sanghuangporus baumii (Pilát) L.W. Zhou & Y.C. Dai, a popular medicinal fungus, has been used to treat several diseases by its triterpenoids bioactive ingredient for many years. However, the triterpenoids content of S. baumii is low and their biosynthesis mechanisms are not clearly understood. I...

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Main Authors: Zengcai Liu, Tingting Sun, Shixin Wang, Li Zou
Format: Article
Language:English
Published: Taylor & Francis Group 2020-01-01
Series:Biotechnology & Biotechnological Equipment
Subjects:
Online Access:http://dx.doi.org/10.1080/13102818.2020.1792342
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spelling doaj-56a20c1f2ca043dba8c4a4921d642ba52020-12-07T14:56:58ZengTaylor & Francis GroupBiotechnology & Biotechnological Equipment1310-28181314-35302020-01-0134162363010.1080/13102818.2020.17923421792342Cloning, molecular properties and differential expression analysis of the isopentenyl diphosphate isomerase gene in Sanghuangporus baumiiZengcai Liu0Tingting Sun1Shixin Wang2Li Zou3Department of Forest Protection, College of Forestry, Northeast Forestry UniversityDepartment of Food Science and Engineering, College of Food Engineering, Harbin UniversityDepartment of Forest Protection, College of Forestry, Northeast Forestry UniversityDepartment of Forest Protection, College of Forestry, Northeast Forestry UniversitySanghuangporus baumii (Pilát) L.W. Zhou & Y.C. Dai, a popular medicinal fungus, has been used to treat several diseases by its triterpenoids bioactive ingredient for many years. However, the triterpenoids content of S. baumii is low and their biosynthesis mechanisms are not clearly understood. In order to reveal the regulation mechanism of triterpenoids biosynthesis in S. baumii, the cDNA encoding isopentenyl diphosphate isomerase (IDI) involved in triterpenoids biosynthesis was cloned and named as SbIDI (GenBank number MK955885). The open reading frame of the SbIDI gene cDNA comprised 792 bp and encoded a polypeptide of 263 amino acids with a predicted protein molecular weight of 29.80 kDa. The transcript level of the SbIDI gene and triterpenoids content of S. baumii were detected at different developmental stages. The results showed that the transcript level of the SbIDI gene and triterpenoids content had almost the same trend of change, increased first and then decreased dynamically. The highest transcript level of the SbIDI gene occurred earlier than the highest triterpenoids content, indicating that the SbIDI gene may play an important role in triterpenoids biosynthesis in S. baumii. Moreover, the SbIDI gene cDNA was successfully expressed in Escherichia coli BL21 (DE3), and the protein bands were consistent with the prediction.The results will lay a foundation for further study of the function of the SbIDI gene.http://dx.doi.org/10.1080/13102818.2020.1792342sanghuangporus baumiiisopentenyl diphosphate isomerasetriterpenoidsbioinformatics analysisexpression analysis
collection DOAJ
language English
format Article
sources DOAJ
author Zengcai Liu
Tingting Sun
Shixin Wang
Li Zou
spellingShingle Zengcai Liu
Tingting Sun
Shixin Wang
Li Zou
Cloning, molecular properties and differential expression analysis of the isopentenyl diphosphate isomerase gene in Sanghuangporus baumii
Biotechnology & Biotechnological Equipment
sanghuangporus baumii
isopentenyl diphosphate isomerase
triterpenoids
bioinformatics analysis
expression analysis
author_facet Zengcai Liu
Tingting Sun
Shixin Wang
Li Zou
author_sort Zengcai Liu
title Cloning, molecular properties and differential expression analysis of the isopentenyl diphosphate isomerase gene in Sanghuangporus baumii
title_short Cloning, molecular properties and differential expression analysis of the isopentenyl diphosphate isomerase gene in Sanghuangporus baumii
title_full Cloning, molecular properties and differential expression analysis of the isopentenyl diphosphate isomerase gene in Sanghuangporus baumii
title_fullStr Cloning, molecular properties and differential expression analysis of the isopentenyl diphosphate isomerase gene in Sanghuangporus baumii
title_full_unstemmed Cloning, molecular properties and differential expression analysis of the isopentenyl diphosphate isomerase gene in Sanghuangporus baumii
title_sort cloning, molecular properties and differential expression analysis of the isopentenyl diphosphate isomerase gene in sanghuangporus baumii
publisher Taylor & Francis Group
series Biotechnology & Biotechnological Equipment
issn 1310-2818
1314-3530
publishDate 2020-01-01
description Sanghuangporus baumii (Pilát) L.W. Zhou & Y.C. Dai, a popular medicinal fungus, has been used to treat several diseases by its triterpenoids bioactive ingredient for many years. However, the triterpenoids content of S. baumii is low and their biosynthesis mechanisms are not clearly understood. In order to reveal the regulation mechanism of triterpenoids biosynthesis in S. baumii, the cDNA encoding isopentenyl diphosphate isomerase (IDI) involved in triterpenoids biosynthesis was cloned and named as SbIDI (GenBank number MK955885). The open reading frame of the SbIDI gene cDNA comprised 792 bp and encoded a polypeptide of 263 amino acids with a predicted protein molecular weight of 29.80 kDa. The transcript level of the SbIDI gene and triterpenoids content of S. baumii were detected at different developmental stages. The results showed that the transcript level of the SbIDI gene and triterpenoids content had almost the same trend of change, increased first and then decreased dynamically. The highest transcript level of the SbIDI gene occurred earlier than the highest triterpenoids content, indicating that the SbIDI gene may play an important role in triterpenoids biosynthesis in S. baumii. Moreover, the SbIDI gene cDNA was successfully expressed in Escherichia coli BL21 (DE3), and the protein bands were consistent with the prediction.The results will lay a foundation for further study of the function of the SbIDI gene.
topic sanghuangporus baumii
isopentenyl diphosphate isomerase
triterpenoids
bioinformatics analysis
expression analysis
url http://dx.doi.org/10.1080/13102818.2020.1792342
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