Zobrazeno 1 - 10
of 52
pro vyhledávání: '"DANIEL E TORRES"'
Publikováno v:
Revista Chilena de Historia Natural, Vol 84, Iss 2, Pp 301-302 (2011)
Externí odkaz:
https://doaj.org/article/17ddf07625d948bb8eccc0bdd3cad2f0
Autor:
Marcos César de Oliveira Santos, Jorge Acevedo, Daniel E. Torres, Alexandre F. Azevedo, Eduardo R. Secchi, Anelio Aguayo-Lobo, Luciano Dalla Rosa, Manuela Bassoi
Publikováno v:
Polar Biology. 43:1-15
The Drake Passage (DP) is a dynamic oceanographic region influenced by the main frontal systems of the Southern Ocean, with little information about cetacean distribution and their relationship with environmental parameters. This study explored the u
Autor:
Alejandro R. Vila, Paola Acuña, Anelio Aguayo-Lobo, Daniel E. Torres, Jorge Acevedo, Benjamín Cáceres, JL Brito, M Cardeña
The eastern South Pacific southern elephant seal population was extinguished by extensive hunting and the current presence of this species in this area is not well understood. We reviewed existing records from the 1900s to 2014 in the eastern South P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9e8bcf5760b15793d8cf9dd0f375b89
Publikováno v:
Polar Biology. 35:469-473
A vagrant adult male Subantarctic fur seal Arctocephalus tropicalis was observed among Antarctic fur seals A. gazella at Cape Shirreff, Livingston Island, Antarctica, which is located to ~4,190 and ~5,939 km from the nearest breeding colonies of Suba
Autor:
Martin Weik, Marco W. Fraaije, Hanna M. Dudek, C. Martinoli, Daniel E. Torres Pazmino, Andrea Mattevi, R. Orru, Antoine Royant
Publikováno v:
Journal of Biological Chemistry. 286:29284-29291
Baeyer-Villiger monooxygenases catalyze the oxidation of carbonylic substrates to ester or lactone products using NADPH as electron donor and molecular oxygen as oxidative reactant. Using protein engineering, kinetics, microspectrophotometry, crystal
Publikováno v:
The Journal of Biological Chemistry, 285(45), 35021-35028. AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
Journal of Biological Chemistry
Journal of Biological Chemistry
The reactivity of flavoenzymes with dioxygen is at the heart of a number of biochemical reactions with far reaching implications for cell physiology and pathology. Flavin-containing monooxygenases are an attractive model system to study flavin-mediat
Autor:
Gonzalo de Gonzalo, Marco W. Fraaije, Daniel E. Torres Pazmino, Vicente Gotor, Ana Rioz-Martínez
Publikováno v:
European Journal of Organic Chemistry, 2010(33), 6409-6416. WILEY-V C H VERLAG GMBH
Optically active sulfoxides are compounds of high interest in organic chemistry. Herein, we report the preparation of a set of chiral heteroaryl alkyl, cyclohexyl alkyl, and alkyl alkyl sulfoxides by using enantioselective sulfoxidation reactions emp
Autor:
Marco W. Fraaije, Gonzalo de Gonzalo, Ana Rioz-Martínez, Daniel E. Torres Pazmino, Vicente Gotor
Publikováno v:
Journal of Organic Chemistry, 75(6), 2073-2076. AMER CHEMICAL SOC INC
Baeyer-Villiger monooxygenases have been tested in the oxidation of racemic benzofused ketones. When employing a single Mutant of phenylacetone monooxygenase (M446G PAMO) under the proper reaction conditions, it was possible to achieve 3-substituted
Publikováno v:
Applied Microbiology and Biotechnology
Applied Microbiology and Biotechnology, 86(5), 1419-1430. SPRINGER
Applied Microbiology and Biotechnology, 86(5), 1419-1430. SPRINGER
DyP-type peroxidases comprise a novel superfamily of heme-containing peroxidases which is unrelated to the superfamilies of known peroxidases and of which only a few members have been characterized in some detail. Here, we report the identification a
Autor:
Daniel E. Torres Pazmino, Gonzalo de Gonzalo, Vicente Gotor, Cristina Rodríguez, Marco W. Fraaije
Publikováno v:
Tetrahedron: Asymmetry
Tetrahedron-Asymmetry, 20(10), 1168-1173. PERGAMON-ELSEVIER SCIENCE LTD
Tetrahedron-Asymmetry, 20(10), 1168-1173. PERGAMON-ELSEVIER SCIENCE LTD
The application of three BVMOs for the enantioselective oxidation of 3-phenylbutan-2-ones with different substituents in the aromatic moiety is described. By choosing the appropriate biocatalyst and substrate combination, chiral ketones and esters ca