G. Chilosi et P. Magro, Pectolytic enzymes produced in vitro and during colonization of melon tissues by Didymella bryoniae, PLANT PATH, 47(6), 1998, pp. 700-705
Pectolytic enzymes produced by Didymella bryoniae in a liquid medium contai
ning pectin as sole carbon source and in inoculated etiolated hypocotyls of
10 melon cultivars, as well as those constitutively expressed in spores, w
ere studied by isoelectric focusing, quantitatively and qualitatively. Five
constitutive pectin lyase (PNL) isoenzymes differing in isoelectric joint
(pI), one acidic (pI 3.9) and four basic (pI 8.4, 8.9, 9.3, 9.9) were expre
ssed in extracts from spores. The same PNL isoenzyme pattern was detected i
n culture filtrates and in infected tissues of all the melon cultivars test
ed. Polygalacturonase (PG) activity, represented by a single inducible acid
ic band (pI 4.6) was detected only in culture filtrates. A single constitut
ive basic pectin methylesterase (PME) isoenzyme (pI > 10.0) was also found
in spores, culture filtrates and inoculated melon tissues. All cultivars we
re susceptible at the seedling growth stage, but with differences in diseas
e severity; cultivars Amarillo Oro and Juane Canari were, respectively, the
least and most susceptible. Pectin lyase activity was highly correlated wi
th disease severity. In rotted tissues and culture filtrates, an increase i
n pH to values over 7.0 was recorded, values optimal for PNL activity. In t
his plant-pathogen interaction, PNL activity represents the principal pecto
lytic component and these isoenzymes were associated with the onset of dise
ase, disease severity and an increase in pH of infected tissue.