Screening of novel chemical compounds as possible inhibitors of carbonic anhydrase and photosynthetic activity of photosystem II

被引:12
|
作者
Karacan, Mehmet Sayim [1 ]
Zharmukhamedov, Sergei K. [2 ]
Mamas, Serhat [1 ]
Kupriyanova, Elena V. [3 ]
Shitov, Alexandr V. [2 ]
Klimov, Vyacheslav V. [2 ]
Ozbek, Neslihan [4 ]
Ozmen, Ummuhan [1 ]
Gunduzalp, Ayla [1 ]
Schmitt, Franz-Josef [5 ]
Karacan, Nurcan [1 ]
Friedrich, Thomas [5 ]
Los, Dmitry A. [3 ]
Carpentier, Robert [6 ]
Allakhverdiev, Suleyman I. [2 ,3 ]
机构
[1] Gazi Univ, Fac Sci, Dept Chem, TR-06500 Ankara, Turkey
[2] Russian Acad Sci, Inst Basic Biol Problems, Pushchino 142290, Moscow Region, Russia
[3] Russian Acad Sci, Inst Plant Physiol, Moscow 127276, Russia
[4] Ahi Evran Univ, Fac Educ, Dept Primary Educ, TR-40100 Kirsehir, Turkey
[5] Tech Univ Berlin, Inst Chem, Max Volmer Lab Biophys Chem, D-10623 Berlin, Germany
[6] Univ Quebec Trois Rivieres, Dept Chim Biochim & Phys, Trois Rivieres, PQ G9A 5H7, Canada
基金
俄罗斯基础研究基金会;
关键词
Carbonic anhydrase; Photosystem II; New inhibitors; Carbonic anhydrase inhibitors; Photosynthetic inhibitors; CHLAMYDOMONAS-REINHARDTII; ANTIBACTERIAL ACTIVITY; THYLAKOID MEMBRANE; ELECTRON-TRANSFER; PEA THYLAKOIDS; HIGHER-PLANTS; GREEN-ALGAE; MANGANESE; DERIVATIVES; NICKEL(II);
D O I
10.1016/j.jphotobiol.2013.12.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Thirty novel chemical compounds were designed and synthesized expecting that they would be possible inhibitors. From this number eleven were organic bases, twenty-four were their organic derivatives and fourteen were metal complexes. Screening of these chemicals by their action on photosynthetic electron transfer (PET) and carbonic anhydrase (CA) activity (CAA) of photosystem II (PSII), alpha-CA, as well as beta-CA was done. Several groups were revealed among them. Some of them are capable to suppress either one, two, three, or even all of the measured activities. As example, one of the Cu(II)-phenyl sulfonylhydrazone complexes (compound 25) suppresses CAA of alpha-CA by 88%, CAA of beta-CA by 100% inhibition; CAA of PSII by 100% and the PSII photosynthetic activity by 66.2%. The Schiff base compounds (12,15) and Cu(II)-phenyl sulfonylhydrazone complexes (25, 26) inhibited the CAA and PET of PSII significantly. The obtained data indicate that the PSII donor side is a target of the inhibitory action of these agents. Some physico- or electrochemical properties such as diffusion coefficient, number of transferred electrons, peak potential and heterogeneous standard rate constants of the compounds were determined in nonaqueous media. pKa values were also determined in nonaqueous and aqueous media. Availability in the studied group of novel chemical agents possessing different inhibitory activity allow in future to isolate the "active part" in the structure of the inhibitors responsible for different inhibitory mechanisms, as well as to determine the influence of side substituters on its inhibitory efficiency. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:156 / 167
页数:12
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