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1.
Genet. mol. res. (Online) ; Genet. mol. res. (Online);5(1): 216-223, Mar. 31, 2006. graf, ilus
Article de Anglais | LILACS | ID: lil-449131

RÉSUMÉ

During its biosynthesis in developing Canavalia brasiliensis seeds, the lectin ConBr undergoes a form of protein splicing in which the order of the N- and C-domains of the protein is reversed. To investigate whether these events can occur in other eukaryotic organisms, an expression system based on Pichia pastoris cells was established. A DNA fragment encoding prepro-ConBr was cloned into the vector pPICZB, and the recombinant plasmid was transformed in P. pastoris strain GS115. Ten clones were screened for effective recombinant protein production. Based on Western blot analysis of the two clones with the highest level of protein expression: 1) diffuse high-molecular mass immunoreactive bands were produced as early as 24 h after induction; 2) a single-, high-molecular mass protein was secreted into the medium, and 3) a significant fraction of the recombinant polypeptides that cross-reacted with anti-ConBr antibodies comprised a band of approximately 34.5 kDa. Diffuse protein bands with high molecular masses are attributed to hyperglycosylation at the single potential N-glycosylation site located in the linker peptide of prepro-ConBr. In contrast, native ConBr is made up of three polypeptides, the intact alpha chain (aa 1-237) and the fragments beta (aa 1-118) and gamma (aa 119-237), which have apparent molecular masses of 30, 16 and 12 kDa, respectively. Apparently, the yeast P. pastoris is not able to carry out all the complex post-translational proteolytic processing necessary for the biosynthesis of ConBr.


Sujet(s)
Canavalia/composition chimique , Lectines végétales/génétique , Modèles génétiques , Pichia/métabolisme , Épissage des protéines/génétique , Régulation de l'expression des gènes végétaux/génétique , Lectines végétales/biosynthèse , Lectines végétales/composition chimique , Réaction de polymérisation en chaîne , Vecteurs génétiques , Technique de Western
2.
Genet. mol. res. (Online) ; Genet. mol. res. (Online);3(1): 117-133, Mar. 2004.
Article de Anglais | LILACS | ID: lil-417579

RÉSUMÉ

The complete genome sequence of the free-living bacterium Chromobacterium violaceum has been determined by a consortium of laboratories in Brazil. Almost 500 open reading frames (ORFs) coding for transport-related membrane proteins were identified in C. violaceum, which represents 11 of all genes found. The main class of transporter proteins is the primary active transporters (212 ORFs), followed by electrochemical potential-driven transporters (154 ORFs) and channels/pores (62 ORFs). Other classes (61 ORFs) include group translocators, transport electron carriers, accessory factors, and incompletely characterized systems. Therefore, all major categories of transport-related membrane proteins currently recognized in the Transport Protein Database (http://tcdb.ucsd.edu/tcdb) are present in C. violaceum. The complex apparatus of transporters of C. violaceum is certainly an important factor that makes this bacterium a dominant microorganism in a variety of ecosystems in tropical and subtropical regions. From a biotechnological point of view, the most important finding is the transporters of heavy metals, which could lead to the exploitation of C. violaceum for bioremediation


Sujet(s)
Chromobacterium/génétique , Cadres ouverts de lecture/génétique , Protéines de transport membranaire/génétique , Chromobacterium/métabolisme , Protéines de transport membranaire/classification , Transport biologique/génétique
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