Properties and secretory mechanism of Musca domestica digestive chymotrypsin and its relation with Drosophila melanogaster homologs
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
01/11/2013
01/11/2013
2012
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Resumo |
Musca domestica larvae present two different digestive chymotryptic activities found in the posterior midgut (PMG): one major soluble activity in the lumen and another minor present in cell membrane fractions. Both soluble and membrane-bound chymotryptic activities have different half lives of thermal inactivation (46 degrees C) in the presence and absence of 10 mM Triton X-100, indicating that they are two different molecular species. Purified soluble chymotryptic activity has pH optimum 7.4 and a molecular mass of 28 kDa in SDS-PAGE. It does not cleave short substrates, such as Suc-F-MCA, preferring longer substrates, such as Suc-AAPF-MCA, with a primary specificity (kcat/Km) for Phe rather than Tyr and Leu residues. In-gel activity revealed a unique band against S-AAPF-MCA with the same migration as purified chymotrypsin. One chymotrypsinogen-like sequence (MdChy1) was sequenced, cloned and recombinantly expressed in Escherichia coli (DE3) Star. MdChy1 is expressed in the proximal posterior midgut (PMG1), as seen by RT-PCR. Expression analysis of other chymotrypsin genes revealed genes expressed at the anterior midgut (AMG) and PMG. Western blot of M. domestica midgut tissues using anti-MdChy1 antiserum showed a single band in samples from AMG and PMG, co-migrating with recombinant and purified enzymes. Immunogold labeling corresponding to Mdchy1 was found in small vesicles (thus indicating exocytosis) and in the lumen of AMG and PMG, corroborating the existence of two similar groups of chymotrypsins. Transcriptomes of M. domestica AMG and whole midgut prepared by pyrosequencing disclosed 41 unique sequences of chymotrypsin-like enzymes (19 probably functional), from which MdChy1 is highly expressed. Phylogenetic reconstruction of Drosophila melanogaster and M. domestica chymotrypsin-like sequences revealed that the chymotrypsin genes expanded before the evolutionary separation of Musca and Drosophila. (C) 2012 Elsevier Ltd. All rights reserved. FAPESP (Tematico) FAPESP (Tematico) CNPq CNPq |
Identificador |
INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY, OXFORD, v. 42, n. 7, supl. 4, Part 1-2, pp. 482-490, JUL, 2012 0965-1748 http://www.producao.usp.br/handle/BDPI/37712 10.1016/j.ibmb.2012.03.005 |
Idioma(s) |
eng |
Publicador |
PERGAMON-ELSEVIER SCIENCE LTD OXFORD |
Relação |
INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY |
Direitos |
closedAccess Copyright PERGAMON-ELSEVIER SCIENCE LTD |
Palavras-Chave | #CHYMOTRYPSIN SEQUENCE #SOLUBLE CHYMOTRYPSIN #MEMBRANE-BOUND CHYMOTRYPSIN #CHYMOTRYPSIN SECRETION #CHYMOTRYPSIN EXPRESSION #DIPTERAN CHYMOTRYPSINS #2 SERINE PROTEASES #LARVAL MIDGUTS #SUBSTRATE-SPECIFICITY #INSECT CHYMOTRYPSINS #BICINCHONINIC ACID #TRYPSIN #EXPRESSION #PROTEINS #ENZYMES #CLONING #BIOCHEMISTRY & MOLECULAR BIOLOGY #ENTOMOLOGY |
Tipo |
article original article publishedVersion |