RESUMO
Fireflies communicate with each other by emitting yellow-green to yellow-orange brilliant light. The bioluminescence reaction, which uses luciferin, Mg-ATP and molecular oxygen to yield an electronically excited oxyluciferin species, is carried out by the enzyme luciferase. Visible light is emitted during relaxation of excited oxyluciferin to its ground state. The high quantum yield of the luciferin/luciferase reaction and the change in bioluminescence colour caused by subtle structural differences in luciferase have attracted much research interest. In fact, a single amino acid substitution in luciferase changes the emission colour from yellow-green to red. Although the crystal structure of luciferase from the North American firefly (Photinus pyralis) has been described, the detailed mechanism for the bioluminescence colour change is still unclear. Here we report the crystal structures of wild-type and red mutant (S286N) luciferases from the Japanese Genji-botaru (Luciola cruciata) in complex with a high-energy intermediate analogue, 5'-O-[N-(dehydroluciferyl)-sulfamoyl]adenosine (DLSA). Comparing these structures to those of the wild-type luciferase complexed with AMP plus oxyluciferin (products) reveals a significant conformational change in the wild-type enzyme but not in the red mutant. This conformational change involves movement of the hydrophobic side chain of Ile 288 towards the benzothiazole ring of DLSA. Our results indicate that the degree of molecular rigidity of the excited state of oxyluciferin, which is controlled by a transient movement of Ile 288, determines the colour of bioluminescence during the emission reaction.
Assuntos
Cor , Vaga-Lumes/enzimologia , Luciferases de Vaga-Lume/química , Luciferases de Vaga-Lume/metabolismo , Luminescência , Animais , Sítios de Ligação , Catálise , Cristalografia por Raios X , Vaga-Lumes/genética , Vaga-Lumes/metabolismo , Interações Hidrofóbicas e Hidrofílicas , Indóis/química , Indóis/metabolismo , Luciferases de Vaga-Lume/genética , Medições Luminescentes , Ácido Lisérgico/análogos & derivados , Ácido Lisérgico/química , Ácido Lisérgico/metabolismo , Modelos Moleculares , Mutação/genética , Conformação Proteica , Pirazinas/química , Pirazinas/metabolismo , Relação Estrutura-AtividadeRESUMO
The carbazole 1,9a-dioxygenase (CARDO) system of Pseudomonas resinovorans strain CA10 catalyzes the dioxygenation of carbazole; the 9aC carbon bonds to a nitrogen atom and its adjacent 1C carbon as the initial reaction in the mineralization pathway. The CARDO system is composed of ferredoxin reductase (CarAd), ferredoxin (CarAc), and terminal oxygenase (CarAa). CarAc acts as a mediator in the electron transfer from CarAd to CarAa. To understand the structural basis of the protein-protein interactions during electron transport in the CARDO system, the crystal structure of CarAc was determined at 1.9 A resolution by molecular replacement using the structure of BphF, the biphenyl 2,3-dioxygenase ferredoxin from Burkholderia cepacia strain LB400 as a search model. CarAc is composed of three beta-sheets, and the structure can be divided into two domains, a cluster-binding domain and a basal domain. The Rieske [2Fe-2S] cluster is located at the tip of the cluster-binding domain, where it is exposed to solvent. While the overall folding of CarAc and BphF is strongly conserved, the properties of their surfaces are very different from each other. The structure of the cluster-binding domain of CarAc is more compact and protruding than that of BphF, and the distribution of electric charge on its molecular surface is very different. Such differences are thought to explain why these ferredoxins can act as electron mediators in respective electron transport chains composed of different-featured components.
Assuntos
Proteínas de Bactérias/química , Dioxigenases/química , Ferredoxinas/química , Pseudomonas/enzimologia , Burkholderia cepacia/enzimologia , Carbono/química , Cristalografia por Raios X , Elétrons , Hidrogênio , Hidrolases/química , Íons , Ferro/química , Modelos Químicos , Modelos Moleculares , Conformação Molecular , Oxigênio/química , Filogenia , Conformação Proteica , Estrutura Secundária de Proteína , Estrutura Terciária de Proteína , Proteômica/métodosRESUMO
FK228 is a histone deacetylase (HDAC) inhibitor, the molecular mechanism of inhibition of which has been unknown. Here we show that reduction of an intramolecular disulfide bond of FK228 greatly enhanced its inhibitory activity and that the disulfide bond was rapidly reduced in cells by cellular reducing activity involving glutathione. Computer modeling suggests that one of the sulfhydryl groups of the reduced form of FK228 (redFK) interacts with the active-site zinc, preventing the access of the substrate. HDAC1 and HDAC2 were more strongly inhibited by redFK than HDAC4 and HDAC6. redFK was less active than FK228 in inhibiting in vivo HDAC activity, due to rapid inactivation in medium and serum. Thus, FK228 serves as a stable prodrug to inhibit class I enzymes and is activated by reduction after uptake into the cells. The glutathione-mediated activation also implicates its clinical usefulness for counteracting glutathione-mediated drug resistance in chemotherapy.
Assuntos
Antibacterianos/farmacologia , Antibióticos Antineoplásicos/farmacologia , Depsipeptídeos , Inibidores Enzimáticos/farmacologia , Inibidores de Histona Desacetilases , Peptídeos Cíclicos , Pró-Fármacos/farmacologia , Sequência de Aminoácidos , Antibacterianos/química , Antibacterianos/farmacocinética , Antibióticos Antineoplásicos/química , Antibióticos Antineoplásicos/farmacocinética , Sítios de Ligação , Biotransformação , Estabilidade de Medicamentos , Inibidores Enzimáticos/química , Inibidores Enzimáticos/farmacocinética , Glutationa/metabolismo , Células HeLa , Humanos , Isoenzimas/antagonistas & inibidores , Modelos Moleculares , Dados de Sequência Molecular , Oxirredução , Pró-Fármacos/química , Pró-Fármacos/farmacocinética , Zinco/metabolismoRESUMO
Two cDNA clones for jasmonic acid (JA)-responsive genes, RRJ1 and RRJ2, were isolated by differential screening from suspension-cultured rice cells treated with JA for 2 h. The putative RRJ1 protein is completely identical to that of a putative rice cystathionine gamma-lyase, while the putative RRJ2 protein is highly similar in sequence to a rice pyruvate decarboxylase, PDC1.
Assuntos
Ciclopentanos/farmacologia , Genes de Plantas , Oryza/genética , Northern Blotting , Células Cultivadas , DNA Complementar , Fases de Leitura Aberta , Oryza/citologia , OxilipinasRESUMO
In Thermus thermophilus homocitrate synthase (HCS) catalyzes the initial reaction of lysine biosynthesis through alpha-aminoadipic acid, synthesis of homocitrate from 2-oxoglutarate and acetyl-CoA. HCS is strongly inhibited by lysine, indicating that the biosynthesis is regulated by the endproduct at the initial reaction in the pathway. HCS also catalyzes the reaction using oxaloacetate in place of 2-oxoglutarate as a substrate, similar to citrate synthase in the tricarboxylic acid cycle. Several other properties of Thermus HCS and an evolutionary relationship of the biosynthetic pathway in the bacterium to other metabolic pathways are also described.