PURIFICATION OF CHYMOTRYPSIN INHIBITORS FROM LARVAL HEMOLYMPH OF THE SILKWORM, BOMBYX-MORI

Citation
T. Shinohara et al., PURIFICATION OF CHYMOTRYPSIN INHIBITORS FROM LARVAL HEMOLYMPH OF THE SILKWORM, BOMBYX-MORI, Bioscience, biotechnology, and biochemistry, 57(7), 1993, pp. 1067-1071
Citations number
27
Categorie Soggetti
Biology,Agriculture,"Biothechnology & Applied Migrobiology","Food Science & Tenology
ISSN journal
09168451
Volume
57
Issue
7
Year of publication
1993
Pages
1067 - 1071
Database
ISI
SICI code
0916-8451(1993)57:7<1067:POCIFL>2.0.ZU;2-T
Abstract
Chymotrypsin inhibitors were purified from larval hemolymph of Bombyx mori. The purification steps involved ammonium sulfate fractionation ( 30-70%) and liquid chromatography on Butyl-Toyopearl 650M, Sephadex G- 75, concanavalin A-Sepharose, Mono-Q, and Mono-S columns. Fourteen iso forms of chymotrypsin inhibitor were resolved in hybrid crosses: ten i soforms from c60 x n511, eight from k03 x FJ1, and nine from i10 x p50 . Chromatographic and electrophoretic studies on the inhibitors sugges ted that they were expressed co-dominantly and could be classified int o three molecular-size groups: 8-13 kDa, 40 kDa, and 42 kDa. CI-b4, CI -13a, CI-13b, and CI-13c in the first group, CI-3 in the second group, and CI-8 in the third group were present in all of the hybrids. Inhib itors in the third size group had an affinity for concanavalin A-Sepha rose. It was found that CI-13 was composed of three different inhibito rs.