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玉米叶片淀粉合酶活性对光照、pH值和氧化还原状态的依赖性。

Dependence of starch synthase activity from maize leaves on light, pH and redox state.

作者信息

Wieweg G H, de Fekete M A

出版信息

Acta Physiol Lat Am. 1976;26(5):415-23.

PMID:28633
Abstract

The starch synthase activity of bundle sheath cells of maize leaves is very low in darkened plants and increases on illumination. In order to find an explanation of these facts we subjected leaf strips, isolated bundle sheath cells and enzymic preparations to pH-changes and to oxidizing or reducing substances. We found that the increase of the activity produced by light could also be caused in the leaf strips by adding malate to the suspending fluid in the dark. On the contrary, with isolated bundle sheath cells no increase with light or with the addition of malate could be observed. There was a decrease of activity due to acidification or to the addition of dichlorophenol-indophenol (DCPIP). The same effect could be observed with enzymic preparations as with the isolated bundle sheath cells, whereas the decrease of activity was higher by acidification of samples coming from darkened plants than for those enzymes prepared from illuminated plants. Also other substances inhibited the synthase activity: benzoquinone, DOPA, caffeic acid, TMPD or Fe (CN6) 3- and PCMB, while only DTE could increase it. After preincubation with PCMB the enzyme activity could be restored with DTE, not so for the preincubation with DCPIP. With an enzymic preparation that contained intact organelles the increase of activity could also be produced by NADH. Thus we follow that the decrease of synthase activity in the darkened plants is due to acidification and to the presence of oxidizing substances, too.

摘要

在黑暗环境下生长的玉米叶片维管束鞘细胞的淀粉合酶活性非常低,光照后活性增加。为了解释这些现象,我们对叶条、分离出的维管束鞘细胞和酶制剂进行了pH值变化以及氧化或还原物质处理。我们发现,在黑暗中向悬浮液中添加苹果酸也能使叶条产生光照所引起的活性增加。相反,对于分离出的维管束鞘细胞,无论是光照还是添加苹果酸,都未观察到活性增加。酸化或添加二氯酚靛酚(DCPIP)会导致活性下降。酶制剂与分离出的维管束鞘细胞表现出相同的效果,然而,来自黑暗环境下植物的样品酸化导致的活性下降比来自光照环境下植物制备的酶更高。其他物质也会抑制合酶活性:苯醌、多巴、咖啡酸、四甲基对苯二胺或铁氰化物以及对氯汞苯甲酸,而只有二硫苏糖醇(DTE)能增加其活性。用对氯汞苯甲酸预孵育后,酶活性可用二硫苏糖醇恢复,而用DCPIP预孵育则不能。对于含有完整细胞器的酶制剂,NADH也能使其活性增加。因此我们得出结论,黑暗环境下植物中合酶活性的下降也是由于酸化和氧化物质的存在。

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