TY - JOUR
T1 - Screening of novel chemical compounds as possible inhibitors of carbonic anhydrase and photosynthetic activity of photosystem II
AU - Karacan, Mehmet Sayim
AU - Zharmukhamedov, Sergei K.
AU - Mamaş, Serhat
AU - Kupriyanova, Elena V.
AU - Shitov, Alexandr V.
AU - Klimov, Vyacheslav V.
AU - Özbek, Neslihan
AU - Özmen, Ümmühan
AU - Gündüzalp, Ayla
AU - Schmitt, Franz Josef
AU - Karacan, Nurcan
AU - Friedrich, Thomas
AU - Los, Dmitry A.
AU - Carpentier, Robert
AU - Allakhverdiev, Suleyman I.
N1 - Funding Information:
This work has been supported partially by The Scientific and Technological Research Council of Turkey (TUBITAK-Project no: 108T317) to M.S.K, and by the grants from Russian Foundation for Basic Research (nos. 13-04-91372, 14-04-01549, 14-04-92690), by Molecular and Cell Biology Programs of the Russian Academy of Sciences, by BMBF (No: 8125) Bilateral Cooperation between Germany and Russia, to S.I.A. T. Friedrich and F.-J. Schmitt acknowledge COST for financial support in the framework of COST action MP1205 and the German Federal Ministry of Education and Research (BMBF, project RUS 11/014).
PY - 2014/8
Y1 - 2014/8
N2 - 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), α-CA, as well as β-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 α-CA by 88%, CAA of β-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.
AB - 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), α-CA, as well as β-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 α-CA by 88%, CAA of β-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.
KW - Carbonic anhydrase
KW - Carbonic anhydrase inhibitors
KW - New inhibitors
KW - Photosynthetic inhibitors
KW - Photosystem II
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U2 - 10.1016/j.jphotobiol.2013.12.002
DO - 10.1016/j.jphotobiol.2013.12.002
M3 - Article
C2 - 24418071
AN - SCOPUS:84904256756
SN - 1011-1344
VL - 137
SP - 156
EP - 167
JO - Journal of Photochemistry and Photobiology B: Biology
JF - Journal of Photochemistry and Photobiology B: Biology
ER -