RICE SCIENCE ›› 2010, Vol. 17 ›› Issue (3): 243-246 .DOI: 10.1016/S1672-6308(09)60023-8

• Short Communication • Previous Articles    

Changes in Activities of Key Enzymes for Starch Synthesis and Glutamine Synthetase in Grains of Progenies from a Rice Cross During Grain Filling

LI Xiao-guang1, 2; LIU Hai-ying3; JIN Zheng-xun1; LIU Hong-liang1; HUANG Xing1; XU Mei-lan1; ZHANG Feng-zhuan1   

  1. 1)College of Agriculture, Northeast Agricultural University, Harbin 150030, China; 2)Tonghua Academy of Agricultural Sciences, Hailong 135007, China; 3Jilin Province Ping’an Seeds Company, Changchun 133000, China
  • Received:2009-08-04 Online:2010-09-28 Published:2010-09-28
  • Contact: JIN Zheng-xun
  • Supported by:
    the Program for Innovative Research Team of Northeast Agricultural University, China and the Project of the Department of Education of Heilongjiang Province, China (Grant No. 11531017).

Abstract: The progenies differed in amylose and protein contents in grains, which derived from a rice cross, Dongnong 423×Toukei 180, were used to study changes in the activities of ADP-glucose pyrophosphorylase (AGPP), soluble starch synthetase (SSS), starch branching enzyme (SBE) and glutamine synthetase (GS) in rice grains during grain filling. The activities of AGPP, SSS and SBE gradually increased and then declined as a single-peak curve with the process of grain filling in the progenies with high and low amylose contents in grains. The progenies with high amylose content peaked earlier in the AGPP, SSS and SBE activities and had higher AGPP, SSS and SBE activities at the early grain filling stage than those with low amylose content. The GS activity peaked earlier and was higher at the late stage of grain filling in the progenies with high protein content than in those with low protein content. It is suggested that the activities of key enzymes for starch synthesis and glutamine synthetase could be changed in oriented breeding for amylose and protein contents in grains.

Key words: rice, hybrid progeny, grain filling, enzyme activity