DocumentCode
2005264
Title
Molecular cloning and characterization analysis of AGP small subunit gene from Dunaliella parva
Author
Shang, Changhua ; Zhu, Shunni ; Yuan, Zhenhong ; Wang, Zhongming
Author_Institution
Key Lab. of Renewable Energy & Natural Gas Hydrate, Guangzhou, China
fYear
2011
fDate
16-18 Sept. 2011
Firstpage
3532
Lastpage
3535
Abstract
ADP-glucose pyrophosphorylase (AGP) plays a key role in regulating starch biosynthesis, which is a heterotetrameric enzyme composed of two large (AGP1) and two small subunits (AGPs). A homology-based PCR was used to clone a cDNA encoding AGP small subunit from Dunaliella parva , which produces starch and lipid. The molecular characterization of the AGPs gene was described. The cDNA of the AGPs (GenBank Accession no. JN033559) was found to contained an open reading frame (ORF) of 1512 bp encoding a 503 amino acid polypeptide. The deduced amino acid sequence of Dunaliella parva AGPs showed significant homology to the known AGPs from Chlamydomonas reinhardtii and Volvox carteri, and contained two conserved domains. The Dunaliella parva AGPs gene cDNA sequence was cloned and its molecular characterization was described by bioinformatics tool. To our knowledge this is the first reported.
Keywords
DNA; biotechnology; enzymes; genetic engineering; ADP-glucose pyrophosphorylase; AGP small subunit gene; Chlamydomonas reinhardtii; Dunaliella parva; Volvox carteri; amino acid sequence; cDNA encoding; heterotetrameric enzyme; homology-based PCR; molecular cloning; open reading frame; starch biosynthesis; Amino acids; Bioinformatics; Cloning; DNA; Genomics; Lipidomics; Proteins; AGP; Dunaliella parva; molecular cloning; sequence analysis;
fLanguage
English
Publisher
ieee
Conference_Titel
Electrical and Control Engineering (ICECE), 2011 International Conference on
Conference_Location
Yichang
Print_ISBN
978-1-4244-8162-0
Type
conf
DOI
10.1109/ICECENG.2011.6058500
Filename
6058500
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