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Molecular cloning and expression of a putative crustacean hyperglycemic hormone of Litopenaeus vannamei in Pichia pastoris
Sánchez-Castrejón, Edna; Ponce-Rivas, Elizabeth; Aguilar, Manuel B; Díaz, Fernando.
  • Sánchez-Castrejón, Edna; Centro de Investigación Científica y de Educación Superior de Ensenada. Departamento de Biotecnología Marina. Ensenada. MX
  • Ponce-Rivas, Elizabeth; Centro de Investigación Científica y de Educación Superior de Ensenada. Departamento de Biotecnología Marina. Ensenada. MX
  • Aguilar, Manuel B; Universidad Nacional Autónoma de México. Instituto de Neurobiología. Laboratorio de Neurofarmacología Marina. Juriquilla. MX
  • Díaz, Fernando; Centro de Investigación Científica y de Educación Superior de Ensenada. Departamento de Biotecnología Marina. Ensenada. MX
Electron. j. biotechnol ; 11(4): 9-10, Oct. 2008. ilus, tab
Artículo en Inglés | LILACS | ID: lil-531925
ABSTRACT
Crustacean hyperglycemic hormone (CHH) is the most abundant and best studied member of the CHH/MIH/GIH neuropeptide hormone family. CHH plays a major role in controlling glucose levels in the hemolymph, and it also has significance in regulating molting, reproduction, and osmoregulation. In contrast, molt-inhibiting hormone (MIH) is responsible for maintaining animals in an intermolt stage. In this study, Liv-MIH-1 cDNA, which encodes a mature neuropeptide from the eyestalk of white shrimp, Litopenaeus vannamei, was expressed in methylotrophic yeast (Pichia pastoris KM71) under the control of an alcohol oxidase promoter. Recombinant Liv-MIH-1 was secreted into the culture medium using the á-factor prepro-sequence without Glu-Ala repeats. The expected protein, which had an apparent molecular mass of 12.1 kDa, was detected by Tricine-SDS-PAGE analysis and confirmed by Western blot. Pure recombinant Liv-MIH-1 was obtained by affinity chromatography, and N-terminal sequence analysis confirmed expression of the protein. Biological assays for CHH and MIH activity were also performed. Purified recombinant Liv-MIH-1 showed the ability to elevate the glucose level of hemolymph of L. vannamei, but molting was unaffected. Since these results are in agreement with the high structural and phylogenetic similarity that has been observed between Liv-MIH-1 and other CHH neuropeptides we propose to rename the protein Liv-CHH-SG1.
Asunto(s)
Texto completo: Disponible Índice: LILACS (Américas) Asunto principal: Ganglios Basales / Proteínas Recombinantes / Crustáceos Idioma: Inglés Revista: Electron. j. biotechnol Asunto de la revista: Biotecnologia Año: 2008 Tipo del documento: Artículo País de afiliación: México Institución/País de afiliación: Centro de Investigación Científica y de Educación Superior de Ensenada/MX / Universidad Nacional Autónoma de México/MX

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Texto completo: Disponible Índice: LILACS (Américas) Asunto principal: Ganglios Basales / Proteínas Recombinantes / Crustáceos Idioma: Inglés Revista: Electron. j. biotechnol Asunto de la revista: Biotecnologia Año: 2008 Tipo del documento: Artículo País de afiliación: México Institución/País de afiliación: Centro de Investigación Científica y de Educación Superior de Ensenada/MX / Universidad Nacional Autónoma de México/MX