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
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.