摘要
在苜蓿(MedicagosativaL.)愈伤组织继代之初加入不同浓度的甲基乙二醛双(脒腙)(MGBG)(0.5,1,2mmol/L),可不同程度地抑制愈伤组织及其后体胚诱导悬浮培养物的生长和体胚形成;若在体胚诱导阶段加入,则上述的抑制作用更为强烈。MGBG不但促进愈伤组织乙烯释放量、内源ACC(1氨基环丙烷1羧酸)水平和ACC合成酶活性,也促进体胚诱导悬浮培养物的ACC水平及ACC合成酶的活性,但降低体胚诱导悬浮培养物的MACC(丙二酰ACC)水平。MGBG对体胚诱导和培养物的生长的抑制作用与其上述的对ACC和乙烯生成促进作用及降低ACC转化成MACC的效应有关。
MGBG [methylglyoxal bis(guanylhydrazone)], when added to the initial of callus subculture, promoted ethylene production in callus grawn in B5h medium, and enhanced the ACC (1aminocyclopropane1carboxylic acid) level and the ACC synthase activity both in the callus grown in B5h medium, and in the suspension cultures in B5g liquid medium for induction of somatic embryogenesis. However, MGBG reduced the malonylACC (MACC) level of the suspension tissues. The treatments of MGBG caused growth of the cultured tissues and induction efficiency of somatic embryogenesis to reduce. Moreover, the effects of MGBG was enhanced when it was added at induction medium of somatic embryogenesis. It could be concluded that this inhibitory effect of MGBG could be due to its promotion of ethylene, ACC levels and ACC synthase activity which has shown to inhibit somatic embryogenesis. The reduction of MACC level could be also involved in the MGBG effect on induction of the embryogenesis.
基金
国家自然科学基金
关键词
苜蓿
体胚发生
乙烯
生物合成
MGBG
Methylglyoxal bis(guanylhydrazone), Medicago sativa, Somatic embryogenesis, Ethylene biosynthesis