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1.
Chinese Journal of Biotechnology ; (12): 1003-1008, 2010.
Article Dans Chinois | WPRIM | ID: wpr-292179

Résumé

Tetraselmis subcordiformis, a marine green alga, can produce hydrogen by photobiologically hydrolyzing seawater with hydrogenase. In this study, the preliminary purification of the enzyme was explored by ammonium sulfate precipitation, and the impact of sodium dithionite, beta-mercaptoethanol and glycerol on the enzyme stability during the process was investigated. The experimental results illustrated that sodium dithionite provided significant protection on the hydrogenase by depleting oxygen, while glycerol, a protectant against the structure instability of the enzyme, also presented protection. Crude enzyme with specific activity of 0.557 U/mg protein was extracted using 60%-70% saturated ammonium sulfate solution supplemented with 200 mmol/L sodium dithionite and 5% glycerol, and the hydrogenase recovery yield was about 30%.


Sujets)
Sulfate d'ammonium , Chimie , Précipitation chimique , Chlorophyta , Stabilité enzymatique , Hydrogène , Métabolisme , Hydrogenase , Métabolisme , Eau de mer
2.
Chinese Journal of Biotechnology ; (12): 297-302, 2007.
Article Dans Chinois | WPRIM | ID: wpr-325376

Résumé

A marine unicellular green alga, Platymonas subcordiformis, was demonstrated to photobiologically produce hydrogen gas from seawater. The objective of this study was to localize and identify the hydrogenase isolated from P. subcordiformis. Adaptation in the presence of inhibitors of protein biosynthesis indicated that the hydrogenase was much more inhibited by cycloheximide than that by chloramphenicol. The result suggested that the hydrogenase isolated from P. subcordiformis is probably synthesized in cytoplasmic ribosomes. Both Western blot analysis and immunogold electron microscopy demonstrate that the P. subcordiformis hydrogenase is mainly located in the chloroplast stroma. The proteins that reacted specifically with the antibodies against the iron hydrogenase isolated from Chlamydomonas reinhardtii were concentrated by immunoprecipitation. The separated protein bands were cut out of the SDS-PAGE gel, in-gel digested by trypsin, and analyzed by Matrix-Assisted Laser Desorption Ionization Time-of-Flight Mass Spectrometry (MALDI-TOF MS). Mascot was employed for analysis of the MALDI data using the public databases NCBInr. The hydrogenase isolated from P. subcordiformis was identified to be the Fe-hydrogenase.


Sujets)
Protéines d'algue , Métabolisme , Biocatalyse , Technique de Western , Chloramphénicol , Pharmacologie , Chlorophyta , Cycloheximide , Pharmacologie , Cytoplasme , Électrophorèse sur gel de polyacrylamide , Hydrogenase , Métabolisme , Immunoprécipitation , Méthodes , Ferrosulfoprotéines , Métabolisme , Cinétique , Microscopie immunoélectronique , Inhibiteurs de la synthèse protéique , Pharmacologie , Spectrométrie de masse MALDI , Méthodes
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