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.

植物病原原核生物中研究得最清楚的是胡卜软腐菌的果裂解酶。

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

与果裂解酶的底物相同。胡卜软腐欧菌的多个亚种产生此酶，但欧菌不产生。

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裂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.

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酸内解。

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解活和异柠檬酸脱氢活是对照的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究得最清楚的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。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，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，缺磷条件下的细胞酸裂解酶活性和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.

植物病原原核生物中研究得最清楚是胡卜软腐菌果胶酸内裂解酶。

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

与果胶酸裂解酶底物相同。胡卜软腐欧氏菌多个亚种产生此酶，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，缺磷条件下细胞异柠檬酸裂解酶活性异柠檬酸脱氢酶活性分别是对照1.4875%。

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是胡卜软果胶酸内裂解酶。

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

与果胶酸裂解酶底物相同。胡卜软欧氏多个亚种此酶，但菊欧氏。

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.

物病原原核生物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，缺磷条件下的细胞酸裂解酶活性和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.

植物病原原核生物中研究得最清胡卜软腐菌果胶酸内裂解酶。

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

与果胶酸裂解酶底物相同。胡卜软腐欧氏菌多个亚种产生此酶，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，缺磷件细胞异柠檬酸裂解酶活性和异柠檬酸脱氢酶活性分别对照1.48倍和75%。