Characterization and Expression Analysis of Starch Branching Enzymes in Sweet Potato

Spatial and temporal expression patterns of Sbe1 and Sbe2 that encode starch branching enzyme (SBE) I and II, respectively, in sweet potato (Ipomoea batatas L.) were analyzed. Expression of both genes in Escherichia coli indicate that both genes encoded active SBE. Analysis with real-time quantitati...

Full description

Bibliographic Details
Main Authors: Hua QIN, Shuang ZHOU, Yi-zheng ZHANG
Format: Article
Language:English
Published: Elsevier 2013-09-01
Series:Journal of Integrative Agriculture
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S209531191360369X
id doaj-c5b72134f42b47d1b5a84a59f91d32db
record_format Article
spelling doaj-c5b72134f42b47d1b5a84a59f91d32db2021-06-07T06:48:43ZengElsevierJournal of Integrative Agriculture2095-31192013-09-0112915301539Characterization and Expression Analysis of Starch Branching Enzymes in Sweet PotatoHua QIN0Shuang ZHOU1Yi-zheng ZHANG2QIN Hua, Correspondence ZHANG Yi-zheng, Tel/Fax: +86-28-85412738; College of Life Sciences, Sichuan University, Chengdu 610064, P.R. ChinaCollege of Life Sciences, Sichuan University, Chengdu 610064, P.R. ChinaQIN Hua, Correspondence ZHANG Yi-zheng, Tel/Fax: +86-28-85412738; College of Life Sciences, Sichuan University, Chengdu 610064, P.R. ChinaSpatial and temporal expression patterns of Sbe1 and Sbe2 that encode starch branching enzyme (SBE) I and II, respectively, in sweet potato (Ipomoea batatas L.) were analyzed. Expression of both genes in Escherichia coli indicate that both genes encoded active SBE. Analysis with real-time quantitative polymerase chain reaction technique indicates that IbSbe1 mRNA was expressed at very low levels in leaves but was the predominant isoform in tuberous root while the reverse case was found for IbSbe2. The expression pattern of IbSbe1, closely resembles that of AGPase S, a gene coding for one of the subunits of ADP-glucose pyrophosphorylase, which is the key regulatory enzyme in the starch biosynthetic pathway. Western analysis detected at least two isoforms of SBE I in tuberous roots, those two isoforms showed adverse expression patterns with the development of the tuberous roots. Expression of the two IbSbe genes exhibited a diurnal rhythm during a 12-h cycle when fed a continuous solution of sucrose. Abscisic acid (ABA) was aother potent inducer of IbSbe expression, but bypassed the semidian oscillator.http://www.sciencedirect.com/science/article/pii/S209531191360369Xsweet potatostarch branching enzymecDNA cloningcDNA expressionexpression patternssucrose induction
collection DOAJ
language English
format Article
sources DOAJ
author Hua QIN
Shuang ZHOU
Yi-zheng ZHANG
spellingShingle Hua QIN
Shuang ZHOU
Yi-zheng ZHANG
Characterization and Expression Analysis of Starch Branching Enzymes in Sweet Potato
Journal of Integrative Agriculture
sweet potato
starch branching enzyme
cDNA cloning
cDNA expression
expression patterns
sucrose induction
author_facet Hua QIN
Shuang ZHOU
Yi-zheng ZHANG
author_sort Hua QIN
title Characterization and Expression Analysis of Starch Branching Enzymes in Sweet Potato
title_short Characterization and Expression Analysis of Starch Branching Enzymes in Sweet Potato
title_full Characterization and Expression Analysis of Starch Branching Enzymes in Sweet Potato
title_fullStr Characterization and Expression Analysis of Starch Branching Enzymes in Sweet Potato
title_full_unstemmed Characterization and Expression Analysis of Starch Branching Enzymes in Sweet Potato
title_sort characterization and expression analysis of starch branching enzymes in sweet potato
publisher Elsevier
series Journal of Integrative Agriculture
issn 2095-3119
publishDate 2013-09-01
description Spatial and temporal expression patterns of Sbe1 and Sbe2 that encode starch branching enzyme (SBE) I and II, respectively, in sweet potato (Ipomoea batatas L.) were analyzed. Expression of both genes in Escherichia coli indicate that both genes encoded active SBE. Analysis with real-time quantitative polymerase chain reaction technique indicates that IbSbe1 mRNA was expressed at very low levels in leaves but was the predominant isoform in tuberous root while the reverse case was found for IbSbe2. The expression pattern of IbSbe1, closely resembles that of AGPase S, a gene coding for one of the subunits of ADP-glucose pyrophosphorylase, which is the key regulatory enzyme in the starch biosynthetic pathway. Western analysis detected at least two isoforms of SBE I in tuberous roots, those two isoforms showed adverse expression patterns with the development of the tuberous roots. Expression of the two IbSbe genes exhibited a diurnal rhythm during a 12-h cycle when fed a continuous solution of sucrose. Abscisic acid (ABA) was aother potent inducer of IbSbe expression, but bypassed the semidian oscillator.
topic sweet potato
starch branching enzyme
cDNA cloning
cDNA expression
expression patterns
sucrose induction
url http://www.sciencedirect.com/science/article/pii/S209531191360369X
work_keys_str_mv AT huaqin characterizationandexpressionanalysisofstarchbranchingenzymesinsweetpotato
AT shuangzhou characterizationandexpressionanalysisofstarchbranchingenzymesinsweetpotato
AT yizhengzhang characterizationandexpressionanalysisofstarchbranchingenzymesinsweetpotato
_version_ 1714536669650092032