TY - JOUR
T1 - Chitinases from Vibrio
T2 - Activity screening and purification of chiA from Vibrio carchariae
AU - Suginta, W.
AU - Robertson, P. A W
AU - Austin, B.
AU - Fry, S. C.
AU - Fothergill-Gilmore, L. A.
PY - 2000
Y1 - 2000
N2 - Fourteen species of Vibrio were screened for chitin-induced chitinase activity in culture medium. V. carchariae, V. alginolyticus 283 and V. campbellii showed high levels of activity. Screening on agar plates containing swollen chitin showed high levels of chitinase activity by the same three species, and also by V. fischeri and V. alginolyticus 284. An affinity purification procedure was developed for the chitinase from V. carchariae. The purified chitinase was active as a monomer with M(r) 63 000- 66 000, and displayed activity toward polymeric chitin from acetylated chitosan or from crab shells. N-terminal sequence analysis and immunological cross-reactivity confirmed that the enzyme belongs to the group A/chiA family of bacterial chitinases.
AB - Fourteen species of Vibrio were screened for chitin-induced chitinase activity in culture medium. V. carchariae, V. alginolyticus 283 and V. campbellii showed high levels of activity. Screening on agar plates containing swollen chitin showed high levels of chitinase activity by the same three species, and also by V. fischeri and V. alginolyticus 284. An affinity purification procedure was developed for the chitinase from V. carchariae. The purified chitinase was active as a monomer with M(r) 63 000- 66 000, and displayed activity toward polymeric chitin from acetylated chitosan or from crab shells. N-terminal sequence analysis and immunological cross-reactivity confirmed that the enzyme belongs to the group A/chiA family of bacterial chitinases.
UR - http://www.scopus.com/inward/record.url?scp=1642551623&partnerID=8YFLogxK
U2 - 10.1046/j.1365-2672.2000.01076.x
DO - 10.1046/j.1365-2672.2000.01076.x
M3 - Article
SN - 1365-2672
VL - 89
SP - 76
EP - 84
JO - Journal of Applied Microbiology
JF - Journal of Applied Microbiology
IS - 1
ER -