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高等植物中与光系统II相关的碳酸酐酶活性位于核心复合体中。

Photosystem II associated carbonic anhydrase activity in higher plants is situated in core complex.

作者信息

Khristin M S, Ignatova L K, Rudenko N N, Ivanov B N, Klimov V V

机构信息

Institute of Basic Biological Problems, Russian Academy of Sciences, Pushchino, 142290 Russia.

出版信息

FEBS Lett. 2004 Nov 5;577(1-2):305-8. doi: 10.1016/j.febslet.2004.10.001.

Abstract

The thylakoid membrane containing photosystem II (PSII membranes) from pea and wheat leaves catalyzed the reaction of CO2 hydration with low rate, which increased after their incubation either with Triton X-100, up to Triton/chlorophyll ratio 1:1, or 1 M CaCl2. The presence of the inhibitor of CAs, p-aminomethylbenzensulfonamide (mafenide), at the start line in the course of electrophoresis of PSII membranes solubilized by n-dodecyl-beta-maltoside (DM) decreased the amount of PSII core complex in the gel. The elution of PSII core complex from the column with immobilized mafenide occurred only either by mafenide or another inhibitor of CAs, ethoxyzolamide. The above results led to a conclusion that membrane-bound CA activity associated with PSII is situated in the core complex.

摘要

来自豌豆和小麦叶片的含有光系统II的类囊体膜(PSII膜)催化CO₂水合反应的速率较低,在用Triton X-100孵育后,该速率会增加,直至Triton/叶绿素比达到1:1,或者用1M CaCl₂孵育后也会增加。在通过正十二烷基-β-麦芽糖苷(DM)溶解的PSII膜电泳过程中,在起始线加入碳酸酐酶(CAs)抑制剂对氨基甲基苯磺酰胺(甲磺灭脓),会减少凝胶中PSII核心复合物的量。用固定化甲磺灭脓从柱上洗脱PSII核心复合物,只能通过甲磺灭脓或另一种CAs抑制剂乙氧苯唑胺来实现。上述结果得出一个结论,即与PSII相关的膜结合CA活性位于核心复合物中。

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