Zucker M, Hankin L
J Bacteriol. 1970 Oct;104(1):13-8. doi: 10.1128/jb.104.1.13-18.1970.
Inducible synthesis of extracellular pectate lyase occurs in Erwinia carotovora, a bacterial soft-rot pathogen of plants, and, to a lesser extent, in a nonpathogenic isolate of Pseudomonas fluorescens. A combination of pectin and a heat-labile factor in fresh potato tissue or acetone powders of the tissue provided the best carbon source for induction. Yields of inducible pectate lyase were much greater than those usually reported. The pathogen, but not the saprophyte, produced a small amount of constitutive enzyme when grown on glucose. The relatively low level or absence of constitutive synthesis in these bacteria did not result from catabolite repression. Attempts were made to relieve any existing catabolite repression by restricting growth through slow feeding of glucose or by growing the organisms on glycerol. These conditions did not significantly alter the differential rate of lyase synthesis compared with changes observed in the presence of inducers. Previous growth history did not affect induction in the pathogen. However, P. fluorescens previously cultured on glucose required 10 to 20 generations of growth on inducing medium before appreciable lyase synthesis occurred. Differences between the pathogen and nonpathogen suggest that regulation of pectate lyase synthesis is related to pathogenicity of soft-rot bacteria.
胞外果胶酸裂解酶的诱导合成发生在胡萝卜软腐欧文氏菌中,它是一种植物细菌性软腐病原菌,在荧光假单胞菌的非致病菌株中也有少量合成。新鲜马铃薯组织或其丙酮粉中的果胶和一种热不稳定因子的组合为诱导提供了最佳碳源。诱导型果胶酸裂解酶的产量远高于通常报道的产量。该病原菌在葡萄糖上生长时会产生少量组成型酶,而腐生菌则不会。这些细菌中组成型合成水平相对较低或不存在并非由分解代谢物阻遏所致。人们试图通过缓慢供给葡萄糖限制生长或让生物体在甘油上生长来解除任何现有的分解代谢物阻遏。与在诱导剂存在下观察到的变化相比,这些条件并未显著改变裂解酶合成的差异速率。先前的生长史对病原菌的诱导没有影响。然而,先前在葡萄糖上培养的荧光假单胞菌在诱导培养基上生长10到20代后才会发生明显的裂解酶合成。病原菌和非病原菌之间的差异表明,果胶酸裂解酶合成的调控与软腐细菌的致病性有关。