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在遭受冷冻胁迫的分离叶肉原生质体中,光合作用碳还原循环的失活。

Inactivation of the photosynthetic carbon reduction cycle in isolated mesophyll protoplasts subjected to freezing stress.

机构信息

Botanisches Institut der Universität Düsseldorf, Universitätsstrasse 1, D-4000, Düsseldorf 1, Federal Republic of Germany.

出版信息

Photosynth Res. 1987 Jan;14(2):137-45. doi: 10.1007/BF00032318.

Abstract

Isolated mesophyll protoplasts from Valerianella locusta L. were subjected to freeze-thaw cycles. Subsequently, steady-state pool sizes of (14)C-labeled intermediates of the photosynthetic carbon reduction cycle were determined by high performance liquid chromatography. Protoplasts in which CO2 fixation was inhibited by preceding freezing stress, showed a strong increase in the proportion of fructose-1,6-bisphosphate, sedoheptulose-1,7-bisphosphate and triose phosphates. These results indicate an inhibition of the activities of stromal fructose-1,6-bisphosphatase and sedoheptulose-1,7-bisphosphatase. Furthermore, freezing stress caused a slight increase in the proportion of labeled ribulose-1,5-bisphosphate, which may be based on an inhibition or ribulose bisphosphate carboxylase activity. It was shown earlier (Rumich-Bayer and Krause 1986) that freezing-thawing readily affects photosynthetic CO2 assimilation independently of thylakoid inactivation. The present results are interpreted in terms of an inhibition of the light-activation system of the photosynthetic carbon reduction cycle, caused by freezing stress.

摘要

从独活中分离出的叶肉原生质体经历了冻融循环。随后,通过高效液相色谱法测定了光合作用碳还原循环中(14)C 标记中间产物的稳态池大小。先前的冷冻胁迫抑制了 CO2 固定的原生质体,果糖-1,6-二磷酸、景天庚酮糖-1,7-二磷酸和三磷酸的比例明显增加。这些结果表明基质果糖-1,6-二磷酸酶和景天庚酮糖-1,7-二磷酸酶的活性受到抑制。此外,冷冻胁迫导致标记的核酮糖-1,5-二磷酸的比例略有增加,这可能基于核酮糖双磷酸羧化酶活性的抑制。早些时候(Rumich-Bayer 和 Krause,1986)表明,冻融过程很容易影响光合作用的 CO2 同化,而不影响类囊体失活。根据冷冻胁迫引起光合作用碳还原循环的光激活系统的抑制,对这些结果进行了解释。

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