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1.
J Exp Bot ; 51(343): 265-74, 2000 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-10938832

RESUMO

An atrazine-tolerant mutant and an atrazine-sensitive cultivar of Brassica napus L. were grown under visible radiation (400 mumol m-2 s-1, photosynthetically active radiation, PAR) and then subjected to treatment conditions. These included short-term high PAR (1600 mumol m-2 s-1) which was given for 4 h either alone or in combination with an enhanced level of UV-BBE radiation (4.6 kJ m-2 h-1 biologically effective UV-B, 280-320 nm). Recovery from the radiation treatment was studied for 4 h under the light conditions for growth. Since it is known that the atrazine-tolerant mutant is susceptible to photoinhibition, one of the aims of the present study was to determine the effects of a supplemental, enhanced level of UV-B radiation with regard to the mutant. The results indicate an additive effect of UV-B radiation on Fv/Fm, photochemical yield and photosynthetic oxygen evolution during both exposure and recovery, and also a higher susceptibility of the mutant to photoinhibitory PAR conditions alone and in combination with UV-B, which may have implications in a changing environment. Both cultivars also showed a higher D1 turnover during the radiation stress than during recovery, as shown by immunoblotting and 35S-methionine incorporation measurements.


Assuntos
Atrazina/farmacologia , Brassica/efeitos da radiação , Luz , Fotossíntese/efeitos da radiação , Raios Ultravioleta , Adaptação Fisiológica , Brassica/efeitos dos fármacos , Brassica/fisiologia , Pigmentos Biológicos
2.
Regul Pept ; 65(1): 11-4, 1996 Aug 27.
Artigo em Inglês | MEDLINE | ID: mdl-8876030

RESUMO

A structurally novel series of cholecystokinin-B (CCK-B) receptor ligands has been designed and synthesized based on the 'double ring system' theory of receptor recognition. Compounds 2b-cis and 2g-cis from this 1-amino-2-benzyltetralin series show modest CCK-B receptor affinity, with IC50 values of 48.5 nM and 39.0 nM, respectively. The results are discussed in the context of ongoing efforts to identify the CCK-B receptor binding site for nonpeptide ligands.


Assuntos
Receptores da Colecistocinina/metabolismo , Sítios de Ligação , Fenômenos Químicos , Físico-Química , Desenho de Fármacos , Modelos Moleculares , Conformação Proteica , Receptor de Colecistocinina B , Receptores da Colecistocinina/química
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