TY - JOUR
T1 - Cobalt(ll) coordination compounds of ethyl 4-methyl-5-imidazolecarboxylate
T2 - Chemical and biochemical characterization on photosynthesis and seed germination
AU - King-Díaz, Beatriz
AU - Montes-Ayala, Josefina
AU - Escartín-Guzmán, Concepción
AU - Castillo-Blum, Silvia E.
AU - Iglesias-Prieto, Roberto
AU - Lotina-Hennsen, Blas
AU - Barba-Behrens, Norah
N1 - Funding Information:
King-Díaz Beatriz 1 Montes-Ayala Josefina 2 Escartín-Guzmán Concepción 2 Castillo-Blum Silvia E. 2 Iglesias-Prieto Roberto 3 Lotina-Hennsen Blas 1 Barba-Behrens Norah [email protected] 2 1 Departamento de Bioquímica Facultad de Quimica Universidad Nacional Autónoma de México. C. U. Coyoacán México D. F. 04510 Mexico unam.mx 2 Departamento de Química Inorgánica Facultad de Quimica Universidad Nacional Autónoma de México. C. U. Coyoacán México D. F. 04510 Mexico unam.mx 3 Estación de Investigaciones Marinas “Puerto Morelos” ICMyL-UNAM. Apartado Postal 1152 Cancún, Quintana Roo 77500 Mexico 2005 3 1-2 93 108 2005 Copyright © 2005 Hindawi Publishing Corporation This is an open access article distributed under the Creative Commons Attribution License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. In this work we present the synthesis, structural and spectroscopic characterization of Co 2+ coordination compounds with ethyl 4-methyl-5-imidazolecarboxylate (emizco). The effects of emizco, the metal salts CoCl 2 .6 H 2 O , CoBr 2 , Co ( NO 3 ) 2 .6 H 2 O and their metal coordination compounds [ Co ( emizco ) 2 Cl 2 ] , [ Co ( emizco ) 2 Br 2 ] .H 2 O , [ Co ( emizco ) 2 ( H 2 O ) 2 ] ( NO 3 ) 2 .2H 2 O were evaluated on photosynthesis in spinach chloroplasts. Seed germination and seedling growth of the monocotyledonous species Lolium multiflorum and Triticum aestivum and the dicotyledonous species Trifolium alexandrinum and Physalis ixocarpa were also assayed under the effect of the compounds and salts. The results showed that cobalt(II) salts and their emizco coordination compounds inhibit photosynthetic electron flow and ATP-synthesis, behaving as Hill reaction inhibitors. Coordination compounds are more potent inhibitors than the salts. It was found that the salts target is at the b 6 f level while the complexes targets are at Q B (D1)-protein and b 6 f level. The Q B inhibition site was confirmed by variable chlorophyll a fluorescence yield. On the other hand, emizco inhibits seed germination, root and shoot development, in both weed and crop species. Cobalt(II) coordination compounds are the most effective photosynthesis inhibitors, but they are less potent than emizco in germination and seedling growth, while the metal salts are the least active of all. Ethyl 4-methyl-5-imidazolecarboxylate Co 2+ emizco coordination compounds cobalt(II) salts photosynthesis seed germination Dirección General Asuntos del Personal Académico IN213800 Dirección General Asuntos del Personal Académico IN21t5698 http://dx.doi.org/10.13039/501100003141 Consejo Nacional de Ciencia y Tecnología
PY - 2005
Y1 - 2005
N2 - In this work we present the synthesis, structural and spectroscopic characterization of Co2+ coordination compounds with ethyl 4-methyl-5-imidazolecarboxylate (emizco). The effects of emizco, the metal salts CoCl2 .6 H2 O, CoBr2, Co ( NO 3) 2 .6 H2 O and their metal coordination compounds [ Co ( emizco) 2 Cl 2 ], [ Co ( emizco) 2 Br 2 ] .H2 O, [ Co ( emizco) 2 ( H2 O) 2 ] ( NO 3) 2 .2H2 O were evaluated on photosynthesis in spinachchloroplasts. Seed germination and seedling growth of the monocotyledonous species Lolium multiflorum and Triticum aestivum and the dicotyledonous species Trifolium alexandrinum and Physalis ixocarpa were also assayed under the effect of the compounds and salts. The results showed that cobalt(II) salts and their emizco coordination compounds inhibit photosynthetic electron flow and ATP-synthesis, behaving as Hill reaction inhibitors. Coordination compounds are more potent inhibitors than the salts. It was found that the salts target is at the b6f level while the complexes targets are at QB(D1)-protein and b6f level. The QB inhibition site was confirmed by variable chlorophyll a fluorescence yield. On the other hand, emizco inhibits seed germination, root and shoot development, in both weed and crop species. Cobalt(II) coordination compounds are the most effective photosynthesis inhibitors, but they are less potent than emizco in germination and seedling growth, while the metal salts are the least active of all.
AB - In this work we present the synthesis, structural and spectroscopic characterization of Co2+ coordination compounds with ethyl 4-methyl-5-imidazolecarboxylate (emizco). The effects of emizco, the metal salts CoCl2 .6 H2 O, CoBr2, Co ( NO 3) 2 .6 H2 O and their metal coordination compounds [ Co ( emizco) 2 Cl 2 ], [ Co ( emizco) 2 Br 2 ] .H2 O, [ Co ( emizco) 2 ( H2 O) 2 ] ( NO 3) 2 .2H2 O were evaluated on photosynthesis in spinachchloroplasts. Seed germination and seedling growth of the monocotyledonous species Lolium multiflorum and Triticum aestivum and the dicotyledonous species Trifolium alexandrinum and Physalis ixocarpa were also assayed under the effect of the compounds and salts. The results showed that cobalt(II) salts and their emizco coordination compounds inhibit photosynthetic electron flow and ATP-synthesis, behaving as Hill reaction inhibitors. Coordination compounds are more potent inhibitors than the salts. It was found that the salts target is at the b6f level while the complexes targets are at QB(D1)-protein and b6f level. The QB inhibition site was confirmed by variable chlorophyll a fluorescence yield. On the other hand, emizco inhibits seed germination, root and shoot development, in both weed and crop species. Cobalt(II) coordination compounds are the most effective photosynthesis inhibitors, but they are less potent than emizco in germination and seedling growth, while the metal salts are the least active of all.
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U2 - 10.1155/BCA.2005.93
DO - 10.1155/BCA.2005.93
M3 - Article
C2 - 18365092
AN - SCOPUS:33444477233
SN - 1565-3633
VL - 2005
SP - 93
EP - 108
JO - Bioinorganic Chemistry and Applications
JF - Bioinorganic Chemistry and Applications
IS - 1-2
ER -