2010
DOI: 10.1021/jf102129f
|View full text |Cite
|
Sign up to set email alerts
|

Molecular Characterization of Mungbean (Vigna radiata L.) Starch Branching Enzyme I

Abstract: Mungbean (Vigna radiata L. cv. Tainan no. 5) starch branching enzyme I (SBE, EC 2.4.1.18) cDNA, VrsbeI, was cloned, and its expression was characterized. Conserved regions of the family B SBE were used to amplify a full length cDNA of 2208 bp. Phylogeny was analyzed, and the partial 3D structure and functional features were predicted. Catalytic residues were identified in the (α/β)(8)-fold, and a unique loop from F365 to F376 between β3/α3 was located. Gene expression of VrsbeI in seeds during growth showed th… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
4
0

Year Published

2013
2013
2023
2023

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 6 publications
(4 citation statements)
references
References 30 publications
0
4
0
Order By: Relevance
“…Three isoforms of SBE (SBEI, SBEIIa, and SBEIIb) were detected in maize, rice, wheat and barley [25, 3942], while in Vigna radiate [43,44], Ipomoea batatas [45]and Phaseolus vulgaris [46], SBE had been classified into SBE I and SBE II isoforms. In Arabidopsis , SBE I did not expressed and its function was unknown, while SBE II had been classified into SBE 2.1 and SBE 2.2 [47].…”
Section: Discussionmentioning
confidence: 99%
“…Three isoforms of SBE (SBEI, SBEIIa, and SBEIIb) were detected in maize, rice, wheat and barley [25, 3942], while in Vigna radiate [43,44], Ipomoea batatas [45]and Phaseolus vulgaris [46], SBE had been classified into SBE I and SBE II isoforms. In Arabidopsis , SBE I did not expressed and its function was unknown, while SBE II had been classified into SBE 2.1 and SBE 2.2 [47].…”
Section: Discussionmentioning
confidence: 99%
“…The branching enzymes be1 and be2 play different roles in the structure of amylopectin in storage organs [31,46]. The be1 knockout mutants observed display no particular phenotype, except in maize [4,16] where be1 appears to be required for starch mobilization during seed germination, and in Chlamydomonas where be1 mutants are defective for starch catabolism [7,47,48].…”
Section: Discussionmentioning
confidence: 99%
“…In quantitative real time-PCR (qRT-PCR) experiment, gene-specific primers were employed to amplify a set of mungbean phytohormones and housekeeping genes, and their details are presented in Table 4 . For indigenous primers, VrTUB and β-Actin primers were chosen in accordance with Chang et al. (2010) and Sairam et al.…”
Section: Methodsmentioning
confidence: 99%