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XB-ART-24195
Cytotechnology 1992 Jan 01;82:103-8.
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High level expression of a frog alpha-amidating enzyme, AE-II, in cultured cells and silkworm larvae using a Bombyx mori nuclear polyhedrosis virus expression vector.

Kobayashi J , Imanishi S , Inoue H , Ohsuye K , Yamaichi K , Tsuruoka N , Tanaka S .


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A Xenopus laevis peptidyl C-terminal alpha-amidating enzyme (AE-II) gene, modified by deletion of a region encoding the putative membrane-spanning domain and the putative C-terminal cytosolic tail, was expressed in BoMo-15 AIIc insect cells and silkworm larvae using a Bombyx mori baculovirus expression vector system. The expressed enzyme was identified predominantly in the culture medium and the hemolymph of silkworm larvae, indicating successful secretion of the expressed AE-II. The level of recombinant enzyme in the larval hemolymph at 4 days post-infection (40 micrograms/ml) was more than 100-fold the peak levels found in the culture medium (250 ng/ml). The enzyme activity in the larval hemolymph at 4 days post-infection was 3700 units/ml.

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References [+] :
Beaudry, Secreted alpha amidating enzymes are generated by specific posttranslational processing of precursors containing transmembrane domains. 1989, Pubmed