Yamaryo Yoshiki, Kanai Daisuke, Awai Koichiro, Shimojima Mie, Masuda Tatsuru, Shimada Hiroshi, Takamiya Ken-ichiro, Ohta Hiroyuki
Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, 4259 Nagatsuta-cho, Midori-ku, Yokohama, 226-8501 Japan.
Plant Cell Physiol. 2003 Aug;44(8):844-55. doi: 10.1093/pcp/pcg110.
The current research investigated the regulation of monogalactosyldiacylglycerol (MGDG) biosynthesis, catalyzed by MGDG synthase (MGD) (UDP-galactose:1,2-diacylglycerol 3-beta-D-galactosyltransferase; EC 2.4.1.46), during chloroplast development in cucumbers (Cucumis sativus L. cv. Aonagajibai). In etiolated seedlings, white light induced a transient increase in MGD mRNA, followed by a subsequent increase in enzyme activity. MGDG, digalactosyldiacylglycerol (DGDG), and linolenic acid (18 : 3) of both MGDG and DGDG accumulated in a light-dependent manner. Early light-dependent induction of MGD protein was also identified in isolated chloroplasts. When cotyledons were detached from seedlings, these light-induced changes diminished. However, when a synthetic cytokinin, benzyladenine, was added to the detached cotyledons, a transient increase in MGD mRNA and a linear increase in the enzyme activity were induced even in the dark. Galactolipids subsequently accumulated to some extent and 18 : 3 content also increased. MGDG fully accumulated in detached cotyledons with co-treatment of light and a cytokinin. Red light (>600 nm) and far-red light (>700 nm) both induced an increase in MGD mRNA and enzyme activity but far-red light did not induce an accumulation of MGDG. These results suggest that (1). galactolipid biosynthesis is regulated by the cooperation of light and a cytokinin; (2). the accumulation of MGDG requires cytokinin in addition to light; (3). a red light (600-700 nm) dependent factor is necessary for the maximal galactolipid accumulation in addition to increase in MGD transcript and activity.
目前的研究调查了黄瓜(Cucumis sativus L. cv. Aonagajibai)叶绿体发育过程中,由单半乳糖基二酰基甘油(MGDG)合成酶(MGD)(UDP - 半乳糖:1,2 - 二酰基甘油3 - β - D - 半乳糖基转移酶;EC 2.4.1.46)催化的MGDG生物合成的调控机制。在黄化幼苗中,白光诱导MGD mRNA短暂增加,随后酶活性增加。MGDG、双半乳糖基二酰基甘油(DGDG)以及MGDG和DGDG中的亚麻酸(18 : 3)均以光依赖的方式积累。在分离的叶绿体中也鉴定出了早期光依赖的MGD蛋白诱导现象。当子叶从幼苗上分离时,这些光诱导的变化减弱。然而,当向分离的子叶中添加合成细胞分裂素苄基腺嘌呤时,即使在黑暗中也会诱导MGD mRNA短暂增加和酶活性线性增加。随后半乳糖脂在一定程度上积累,18 : 3含量也增加。在光和细胞分裂素共同处理下,MGDG在分离的子叶中完全积累。红光(>600 nm)和远红光(>700 nm)均诱导MGD mRNA和酶活性增加,但远红光不诱导MGDG积累。这些结果表明:(1). 半乳糖脂生物合成受光和细胞分裂素协同调控;(2). MGDG的积累除了光之外还需要细胞分裂素;(3). 除了MGD转录本和活性增加外,红光(600 - 700 nm)依赖因子对于最大程度的半乳糖脂积累是必需的。