中国农业科学 ›› 2010, Vol. 43 ›› Issue (19): 3965-3973 .doi: 10.3864/j.issn.0578-1752.2010.19.008

• 耕作栽培·生理生化·农业信息技术 • 上一篇    下一篇

花生荚果干物质积累与蔗糖代谢的相关性研究

崔光军,刘风珍,万勇善

  

  1. (山东农业大学农学院/作物生物学国家重点实验室)
  • 收稿日期:2010-03-01 修回日期:2010-04-26 出版日期:2010-10-01 发布日期:2010-10-01
  • 通讯作者: 刘风珍,万勇善

Relationship Between Dry Matter Accumulation and Sucrose Metabolism During Pod Development in Peanut (Arachis hypogaea L.)

CUI Guang-jun, LIU Feng-zhen, WAN Yong-shan
  

  1. (山东农业大学农学院/作物生物学国家重点实验室)
  • Received:2010-03-01 Revised:2010-04-26 Online:2010-10-01 Published:2010-10-01
  • Contact: LIU Feng-zhen, WAN Yong-shan

摘要:

【目的】探讨花生荚果产量和籽仁营养成分含量与种子蔗糖代谢的关系。【方法】选用种子发育正常的大花生品系(05D610)及其种子皱缩变异品系(05D677)为材料,测定了果针入土后6—72 d的荚果干重、果针入土后30—72 d籽仁可溶性总糖、蔗糖、果糖、葡萄糖、淀粉、蛋白质、脂肪含量等,以及果针入土后30—66 d籽仁中与蔗糖代谢相关酶活力的动态变化。【结果】果针入土后24—54 d是荚果干重的快速积累时期,是决定荚果干重的关键时期,期间05D610干物质积累速率是05D677的2.4倍。收获期05D610和05D677的荚果干重分别是2.06 g和1.28 g,差异极显著。果针入土后30—72 d时期内,05D610籽仁中己糖/蔗糖比值、脂肪含量显著高于05D677,蛋白质含量显著低于05D677,两品系淀粉含量差异不显著。果针入土后30—66 d时期内,蔗糖合成酶(SS)合成方向的酶活力显著高于蔗糖磷酸合成酶(SPS),是合成蔗糖的主要酶;蔗糖合成酶裂解方向的酶活力显著高于酸性转化酶(AI)和中性转化酶(NI),是裂解蔗糖的主要酶。蔗糖合成酶在花生种子有机物贮藏阶段的蔗糖代谢中占主导作用。两品系间蔗糖合成酶合成方向的酶活力差异不显著,05D610蔗糖磷酸合成酶活力显著高于05D677,05D610蔗糖合成酶裂解方向的酶活力明显低于05D677。【结论】在花生果针入土后24—54 d是干物质积累的关键时期。蔗糖合成酶(裂解方向)是影响有机物积累的关键酶。籽仁中己糖/蔗糖比值、蔗糖磷酸合成酶活力、蔗糖合成酶裂解方向酶活力的差异可能是造成正常品系(05D610)和种子皱缩变异品系(05D677)间荚果干物质积累速率、荚果干重、营养成分出现差异的原因。

关键词: 花生, 荚果发育, 干物质积累, 蔗糖代谢

Abstract:

【Objective】 The experiment aimed at study on the relationship between peanut pod dry matter accumulation and sucrose metabolism. 【Method】 With the seeds of normal peanut line 05D610 and its wrinkled mutant line 05D677 as material, the dynamic changes of pod dry weight (during 6-72 d after peg penetration), contents of soluble sugar, sucrose,fructose,glucose,starch, protein, and oil in seeds (during 6-72 d after peg penetration), and activities of sucrose-metabolizing enzymes (during 30-72 d after peg penetration) were examined. 【Result】 The period of 24-54 d after peg penetration was a rapid dry weight accumulation phase which determined the final dry weight, and pod dry weight accumulation rate of 05D610 was 2.4 times that of 05D677 in the same period. At harvest, dry weight of 05D610 and 05D677 were 2.06 g and 1.28 g, respectively, the difference between them was highly significant. In the period of 30-72 d after peg penetration, hexose/sucrose ratio and oil content of 05D610 seeds were always significantly higher than that of 05D677, while the protein content of 05D610 being always significantly lower than that of 05D677, and the starch content in seeds was not different significantly between 05D610 and 05D677. During the period of seed dry matter accumulation, the activity of sucrose synthase (SS) was significantly higher than that of sucrose phosphate synthase (SPS), which was the main enzyme on sucrose syntheses. SS activity was higher than acid invertase (AI) and neutral invertase (NI), which was also the main enzyme for direction of sucrose cleavage. In conclusion, SS is the main enzyme for sucrose metabolism at the stored matter accumulation stage of peanut seeds. SS (synthesis) activity in seeds showed slight difference between 05D610 and 05D677.SS (cleavage) activity of 05D610 was significantly lower than that of 05D677. SPS activity of 05D610 was significantly higher than that of 05D677. 【Conclusion】 The phase 24-54 d after peg penetration is more important for pod dry weight accumulation. SS (cleavage) is a key enzyme for organic matter accumulation. The difference in hexose/sucrose ratio, SPS activity, SS (cleavage) activity between 05D610 and 05D677 may be the dominant factor leading to their difference in dry weight accumulation rate of pod, pod dry weight and content of components in peanut seeds.

Key words: peanut, pod development, dry matter accumulation, sucrose metabolism