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萝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同。胡萝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的胡萝卜软腐菌的果胶酸内解酶。

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

与果胶酸解酶的底物同。胡萝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，缺磷条件下的细胞异柠檬酸解酶活性和异柠檬酸脱氢酶活性分照的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萝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.

与果胶酸解的底物同。胡萝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楚的是胡萝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.

与果胶解酶的底物同。胡萝卜软腐欧氏菌的多个生此酶，但菊欧氏菌不生。

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.

植物病原原核生物中研究得最清楚是胡萝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同。胡萝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和异柠檬酸脱氢酶活性分别是对1.48和75%。

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

原原核生中研究得最清楚的是胡萝卜软腐菌的果胶内解酶。

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

与果胶解酶的底同。胡萝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，缺磷条件下的细胞异柠解酶活性和异柠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萝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同。胡萝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萝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同。胡萝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和异柠檬酸脱氢酶活性分别是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的是胡萝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同。胡萝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.

8 d，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.

植物病原原核物中研究得最清楚的是胡萝卜软腐菌的内裂解酶。

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

与裂解酶的底物同。胡萝卜软腐欧氏菌的多个亚种酶，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%。