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二苯卡巴肼向光系统II的电子供体作用受到内源性锰复合物和外源性锰离子的抑制。

Electron donation to photosystem II by diphenylcarbazide is inhibited both by the endogenous manganese complex and by exogenous manganese ions.

作者信息

Rashid A, Popovic R

机构信息

Département de chimie, Université du Québec à Montréal, Canada.

出版信息

Biochem Cell Biol. 1995 May-Jun;73(5-6):241-5. doi: 10.1139/o95-029.

Abstract

Diphenylcarbazide (DPC) is an efficient electron donor to the inactive oxygen-evolving complex of photosystem II (PSII). We investigated the role of manganese on the rate of electron donation from DPC to PSII in both Mn-depleted (Tris washed) and Mn-retaining (NaCl washed) PSII preparations. The rate of electron donation from DPC to PSII was significantly higher in Mn-depleted than in Mn-retaining preparations, indicating a negative role of native Mn complex on DPC electron donation. The apparent Km values for DPC were found to be 0.11 and 0.17 mM for Mn-depleted and Mn-retaining PSII preparations, respectively. This difference in the Km values also indicates an antagonistic effect of endogenous Mn cluster on electron donation from DPC, which was markedly inhibited by exogenous Mn2+. However, the magnitude of inhibition was greater in Mn-depleted than in Mn-retaining PSII preparations. This indicates a higher accessibility to DPC to PSII in the absence of native Mn complex. Our results suggest (i) that Mn, either endogenous or added, acts as an accessibility barrier for DPC to donate electrons to PSII and (ii) that the native Mn complex not only functions as an accumulator of oxidizing equivalents but may also protect PSII from exogenous reductants.

摘要

二苯卡巴肼(DPC)是光系统II(PSII)失活的放氧复合体的一种有效电子供体。我们研究了锰在锰耗尽(用Tris洗涤)和保留锰(用NaCl洗涤)的PSII制剂中对DPC向PSII电子供体速率的作用。在锰耗尽的制剂中,DPC向PSII的电子供体速率显著高于保留锰的制剂,这表明天然锰复合体对DPC电子供体有负面作用。对于锰耗尽和保留锰的PSII制剂,DPC的表观Km值分别为0.11和0.17 mM。Km值的这种差异也表明内源性锰簇对DPC电子供体有拮抗作用,外源性Mn2+可显著抑制该作用。然而,在锰耗尽的PSII制剂中抑制程度大于保留锰的制剂。这表明在没有天然锰复合体的情况下,DPC对PSII的可及性更高。我们的结果表明:(i)内源性或添加的锰作为DPC向PSII供电子的可及性屏障;(ii)天然锰复合体不仅作为氧化当量的积累器,还可能保护PSII免受外源性还原剂的影响。

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