Malissard M, Chavagnat F, Duez C, Vacheron M J, Guinand M, Michel G, Ghuysen J M
Laboratoire de Biochimie Microbienne, Université Claude Bernard, Villeurbanne, France.
FEMS Microbiol Lett. 1995 Feb 15;126(2):105-11. doi: 10.1111/j.1574-6968.1995.tb07402.x.
In previous studies (Malissard et al., FEMS Microbiol. Lett. (1993) 110, 101-106), the alginate lyase AlxM of the marine bacterium ATCC 433367 was produced in Escherichia coli TC4/pAL-A3 with a yield of 50 micrograms per litre of culture. The polypeptide chain was cleaved between two cysteine residues, C169 and C183, themselves linked by a disulphide bridge. AlxM has now been overproduced in E. coli BL21(DE3)/pAL-Sur/pLysS. Under conditions in which formation of inclusion bodies can be avoided, the enzyme is synthesized as a catalytically active, water-soluble, unnicked polypeptide with a yield of 32 mg per litre of culture. It has been purified to protein homogeneity using a one-step procedure. The nicked AlxMA and unnicked AlxMB alginate lyases have identical alginate-degrading activities at high salt concentrations.