Microbial exopolysaccharides (EPS) are the substrates for a wide range of e
nzymes most of which are highly specific. The enzymes are either endoglycan
ases or polysaccharide lyases and their specificity is determined by carboh
ydrate structure with uronic acids often playing a major role. The presence
of various acyl substituents frequently has little effect on the action of
many of the polysaccharases but markedly inhibits some of the polysacchari
de lyases including alginate and gellan lyases, The commonest sources of su
ch enzymes can be either microorganisms or bacteriophages. These specific p
olysaccharide-degrading enzymes can yield oligosaccharide fragments, which
are amenable to NMR and other analytical techniques. They have thus proved
to be extremely useful in providing information about microbial polysacchar
ide structures and were routinely used in many such studies. Complex system
s containing various mixtures of enzymes may also be effective in the absen
ce of single enzymes but may be difficult to obtain with reproducible activ
ities. Such preparations may also cause extensive degradation of the polysa
ccharide structure and thus prove less useful in providing information. Com
mercially available enzyme preparations have seldom proved capable of degra
ding microbial heteropolysaccharides, although some are active against bact
erial alginates and homopolysaccharides including bacterial cellulose and c
urdlan. (C) 1999 Elsevier Science Ltd. All rights reserved.