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ACTA HORTICULTURAE SINICA ›› 2016, Vol. 43 ›› Issue (6): 1117-1125.doi: 10.16420/j.issn.0513-353x.2016-0301

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Gene Cloning and Expression Analysis of ADP-glucose Pyrophosphorylase in Colocasia esculenta

WANG Li,YIN Jian-mei*,HAN Xiao-yong,ZHANG Pei-tong,GUO Wen-qi,and LI Chun-hong   

  1. (Institute of Industrial Crops,Jiangsu Academy of Agricultural Sciences,Nanjing 210014,China)
  • Online:2016-06-25 Published:2016-06-25

Abstract:

Based on the transcriptome data of Colocasia esculentaL.Schottfull-length cDNA of ApS1ADP-glucose pyrophosphorylase small subunit 1gene was cloned fromJingjiang Xiangsha Taro’,which consisted of 1 596 bp and encoded a protein of 532 amino acidsand tentatively designated as CeApS1NCBIColocasia KU288757unreleased. CeApS1 contained a NTP_transf_3 domainGly104Pro306and a PbH1 domainGly473Ser515. This gene encoded a small subunit of ADP-glucose pyrophosphorylaseand isoelectric point and molecular weight were 6.73 and 57.6 kDrespectively. Results displayed ApS1 existed in monocotyledons and dicotyledons. BlastX showed that ApS1 in Colocasia esculenta shared 83.4% identity with Landoltia punctateand showed farther phylogenetic relationships with Fragaria ananassaAAS00541.1),Medicago truncatulaXP_003617925.1),Oryza sativaAAK27313.1and Triticum aestivumCAA46879.1. The CeApS1 transcript widely presented in the main cormlateral cormelsleavespetioles and roots of Colocasia esculentaand displayed higher expression levels in taro corms than those in leaves. The results indicated that there was a significantly positive correlation between CeApS1 transcript expression and starch contents in taro corms.

Key words: Colocasia esculenta, starch synthase, gene cloning, expression analysis

CLC Number: