| Literature DB >> 2268291 |
K Yamada1, Y Nakajima, S Natori.
Abstract
A cDNA for sarcotoxin IA, an antibacterial protein of Sarcophaga peregrina (fleshfly), was inserted into a silkworm baculovirus vector and expressed in Bm-N cells, a line of Bombyx mori cells. When a cysteine proteinase inhibitor, p-chloromercuribenzenesulphonic acid, was present in the culture medium, a significant amount of recombinant sarcotoxin IA accumulated, but without this reagent the product seemed to be degraded in this system. The C-terminus of the recombinant sarcotoxin IA seemed to be glycine, not amidated arginine as found in authentic sarcotoxin IA. Probably, Bm-N cells lack the C-terminal alpha-amidation enzyme.Entities:
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Year: 1990 PMID: 2268291 PMCID: PMC1149755 DOI: 10.1042/bj2720633
Source DB: PubMed Journal: Biochem J ISSN: 0264-6021 Impact factor: 3.857