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Low‐Molecular‐Weight Trypsin Inhibitors of Microbial Origin
Author(s) -
Ulezlo IV,
Kuropatki,
Shulgina MV,
Bezborodov AM
Publication year - 1987
Publication title -
biotechnology and applied biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.468
H-Index - 70
eISSN - 1470-8744
pISSN - 0885-4513
DOI - 10.1111/j.1470-8744.1987.tb00477.x
Subject(s) - trypsin , chymotrypsin , autolysis (biology) , chemistry , proteases , biochemistry , chromatography , streptomyces , streptomycetaceae , actinomycetales , enzyme , biology , bacteria , genetics
Three hundred actinomyces cultures newly isolated from the soil of different regions of the Soviet Union were tested for their ability to produce inhibitors of trypsin‐like proteases. Seven previously not known to produce trypsin inhibitors (Streptomyces bikiniensis 17‐5, S. sporoclivatus 28‐1, S. filamentosus 32‐11, S. diastatochromogenes 20‐4, S. lavendulae 29‐4, S. violacens 52‐8, and Streptoverticillium cinnamoneum 36‐8) were found to possess high antitrypsin activity. The morphological and cultural properties of the strains and the dynamics of inhibitor production were investigated. S. bikiniensis 17‐5 was studied in greatest detail. Its culture filtrate contained several inhibitors for trypsin and one for chymotrypsin. A mixture of oligopeptides with Mr of 300–500 was obtained by the described procedure which included the adsorption of the culture fluid filtrate on charcoal followed by ion‐exchange chromatography on CM‐cellulose. Four trypsin inhibitors (Sb‐IT1, Sb‐IT2, Sb‐IT3, and Sb‐IT4) were isolated from the mixture in a highly purified state by reversed‐phase high‐performance liquid chromatography. Sb‐IT2 has been recognized as formylhistidylvaline with an Mr of 282. No trypsin inhibitor of this structure has been described previously.