Yamada K, Nakajima Y, Natori S
Faculty of Pharmaceutical Sciences, University of Tokyo, Japan.
Biochem J. 1990 Dec 15;272(3):633-6. doi: 10.1042/bj2720633.
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.
将麻蝇(肉蝇)的抗菌蛋白——肌毒素IA的互补DNA(cDNA)插入家蚕杆状病毒载体,并在家蚕细胞系Bm - N细胞中表达。当培养基中存在半胱氨酸蛋白酶抑制剂对氯汞苯磺酸时,大量重组肌毒素IA积累,但没有这种试剂时,该产物在这个系统中似乎会被降解。重组肌毒素IA的C末端似乎是甘氨酸,而不是天然肌毒素IA中的酰胺化精氨酸。可能是Bm - N细胞缺乏C末端α-酰胺化酶。