The best studied inducible and repressible enzyme in phytopathogenic prokaryotes is endo-pectate lyase in E. carotovora.

植物病原原核生物中研究得最清楚是胡卜软腐胶酸内裂解酶。

Polygalacturonase has the same substrate specificity as pectate lyase. This enzyme is produced by Erwinia carotovora subspp. but not by Erwinia chyrsanthemi.

与胶酸裂解酶底物相同。胡卜软腐欧氏多个亚种生此酶，但菊欧氏生。

Moreover, the activities of isocitrate lyase and isocitrate dehydrogenase in the 0 P-treated cells were 1.48 and 0.75 times higher than in the control at day 8 of the treatment.

在第8 d，缺磷条件下细胞异柠檬酸裂解酶活性和异柠檬酸脱氢酶活性分别是对照1.48倍和75%。

The best studied inducible and repressible enzyme in phytopathogenic prokaryotes is endo-pectate lyase in E. carotovora.

植物病原原核生物中研究得最清楚的是软腐菌的果胶酸内裂解酶。

Polygalacturonase has the same substrate specificity as pectate lyase. This enzyme is produced by Erwinia carotovora subspp. but not by Erwinia chyrsanthemi.

与果胶酸裂解酶的底物相。软腐欧氏菌的多个亚种产生此酶，但菊欧氏菌不产生。

Moreover, the activities of isocitrate lyase and isocitrate dehydrogenase in the 0 P-treated cells were 1.48 and 0.75 times higher than in the control at day 8 of the treatment.

在第8 d，缺磷条件下的细胞异柠檬酸裂解酶活性和异柠檬酸脱氢酶活性分别是对照的1.48倍和75%。

The best studied inducible and repressible enzyme in phytopathogenic prokaryotes is endo-pectate lyase in E. carotovora.

植物核生物中研究得最清楚的是胡卜软腐菌的果胶酸内裂解。

Polygalacturonase has the same substrate specificity as pectate lyase. This enzyme is produced by Erwinia carotovora subspp. but not by Erwinia chyrsanthemi.

与果胶酸裂解的底物相同。胡卜软腐欧氏菌的多个亚种产生此，但菊欧氏菌不产生。

Moreover, the activities of isocitrate lyase and isocitrate dehydrogenase in the 0 P-treated cells were 1.48 and 0.75 times higher than in the control at day 8 of the treatment.

在第8 d，缺磷条件下的细胞异柠檬酸裂解和异柠檬酸脱氢分别是对照的1.48倍和75%。

The best studied inducible and repressible enzyme in phytopathogenic prokaryotes is endo-pectate lyase in E. carotovora.

病原原核生中研究得最清楚的是胡卜软腐菌的果胶酸内裂解酶。

Polygalacturonase has the same substrate specificity as pectate lyase. This enzyme is produced by Erwinia carotovora subspp. but not by Erwinia chyrsanthemi.

与果胶酸裂解酶的底相同。胡卜软腐欧氏菌的多个亚种产生此酶，但菊欧氏菌不产生。

Moreover, the activities of isocitrate lyase and isocitrate dehydrogenase in the 0 P-treated cells were 1.48 and 0.75 times higher than in the control at day 8 of the treatment.

在第8 d，缺磷条件下的细胞檬酸裂解酶活性檬酸脱氢酶活性分别是对照的1.48倍75%。

The best studied inducible and repressible enzyme in phytopathogenic prokaryotes is endo-pectate lyase in E. carotovora.

植物病原原核生物中研究得最清楚的是胡卜软腐菌的果胶解酶。

Polygalacturonase has the same substrate specificity as pectate lyase. This enzyme is produced by Erwinia carotovora subspp. but not by Erwinia chyrsanthemi.

与果胶解酶的底物相同。胡卜软腐欧氏菌的多个亚种产生此酶，欧氏菌不产生。

Moreover, the activities of isocitrate lyase and isocitrate dehydrogenase in the 0 P-treated cells were 1.48 and 0.75 times higher than in the control at day 8 of the treatment.

在第8 d，缺磷条件下的细胞异柠檬解酶活性和异柠檬脱氢酶活性分别是对照的1.48倍和75%。

The best studied inducible and repressible enzyme in phytopathogenic prokaryotes is endo-pectate lyase in E. carotovora.

病原原核生中研究得最清楚的是胡卜软腐菌的果胶酸内裂解酶。

Polygalacturonase has the same substrate specificity as pectate lyase. This enzyme is produced by Erwinia carotovora subspp. but not by Erwinia chyrsanthemi.

与果胶酸裂解酶的底相同。胡卜软腐欧氏菌的多个亚种产生此酶，但菊欧氏菌不产生。

Moreover, the activities of isocitrate lyase and isocitrate dehydrogenase in the 0 P-treated cells were 1.48 and 0.75 times higher than in the control at day 8 of the treatment.

在第8 d，缺磷条件下的细胞檬酸裂解酶活性檬酸脱氢酶活性分别是对照的1.48倍75%。

The best studied inducible and repressible enzyme in phytopathogenic prokaryotes is endo-pectate lyase in E. carotovora.

植物病原原核生物中研究得最清楚是胡卜软腐酸内裂解酶。

Polygalacturonase has the same substrate specificity as pectate lyase. This enzyme is produced by Erwinia carotovora subspp. but not by Erwinia chyrsanthemi.

与酸裂解酶底物相同。胡卜软腐欧多个亚种产生此酶，但菊欧产生。

Moreover, the activities of isocitrate lyase and isocitrate dehydrogenase in the 0 P-treated cells were 1.48 and 0.75 times higher than in the control at day 8 of the treatment.

在第8 d，缺磷条件下细胞异柠檬酸裂解酶活性和异柠檬酸脱氢酶活性分别是对照1.48倍和75%。

The best studied inducible and repressible enzyme in phytopathogenic prokaryotes is endo-pectate lyase in E. carotovora.

植物病原原核物中研究得最清楚的是胡卜软腐菌的胶酸内裂解。

Polygalacturonase has the same substrate specificity as pectate lyase. This enzyme is produced by Erwinia carotovora subspp. but not by Erwinia chyrsanthemi.

胶酸裂解的底物相同。胡卜软腐欧氏菌的多个亚种，但菊欧氏菌不。

Moreover, the activities of isocitrate lyase and isocitrate dehydrogenase in the 0 P-treated cells were 1.48 and 0.75 times higher than in the control at day 8 of the treatment.

在第8 d，缺磷条件下的细胞异柠檬酸裂解活性和异柠檬酸脱氢活性分别是对照的1.48倍和75%。

The best studied inducible and repressible enzyme in phytopathogenic prokaryotes is endo-pectate lyase in E. carotovora.

植物病原原核生物中研清楚的是胡卜软腐菌的果胶酸内裂解酶。

Polygalacturonase has the same substrate specificity as pectate lyase. This enzyme is produced by Erwinia carotovora subspp. but not by Erwinia chyrsanthemi.

与果胶酸裂解酶的底物相同。胡卜软腐欧氏菌的多个亚种产生此酶，但菊欧氏菌不产生。

Moreover, the activities of isocitrate lyase and isocitrate dehydrogenase in the 0 P-treated cells were 1.48 and 0.75 times higher than in the control at day 8 of the treatment.

在第8 d，缺磷条件下的柠檬酸裂解酶活性和柠檬酸脱氢酶活性分别是对照的1.48倍和75%。