Chatterjee A K, Thurn K K, Tyrell D J
J Bacteriol. 1985 May;162(2):708-14. doi: 10.1128/jb.162.2.708-714.1985.
Mutants of Erwinia chrysanthemi EC16 deficient in the polygalacturonate catabolic enzymes oligogalacturonate lyase (Ogl-) and 3-deoxy-D-glycero-2,5-hexodiulosonate (ketodeoxyuronate) dehydrogenase (KduD-) were obtained by Tn5 mutagenesis using the R plasmid pJB4JI. Ogl- Exu+ (Exu+, D-galacturonate utilization) and KduD- Exu- strains macerated potato tuber tissue and utilized glucose, glycerol, and gluconate, but they did not utilize polygalacturonate, unsaturated digalacturonate, or saturated digalacturonate. Genetic and physical evidence indicated that the Ogl- mutants and a KduD- recombinant contained a single copy of Tn5 and that Tn5 (Kmr) was linked to the mutant phenotypes. In the Ogl+ parents, basal levels of oligogalacturonate lyase were present in glycerol-grown cells and induced levels were present with saturated or unsaturated digalacturonate, while oligogalacturonate lyase was undetectable under similar conditions in Ogl- strains. Pectate lyase, polygalacturonase, and ketodeoxyuronate dehydrogenase were induced in an Ogl- strain by 3-deoxy-D-glycero-2,5-hexodiulosonate and by the enzymatic products of unsaturated digalacturonate but not by the digalacturonates. The KduD- strains lacked the dehydrogenase activity but in the presence of the digalacturonates produced higher levels of pectate lyase, polygalacturonase, and oligogalacturonate lyase than the KduD+ parents did. In the KduD- strains, pectate lyase and oligogalacturonate lyase were induced by unsaturated digalacturonate in a "gratuitous" manner, suggesting an intracellular accumulation of the inducer(s). We conclude that an intermediate(s) of the ketodeoxyuronate pathway induces pectate lyase, polygalacturonase, oligogalacturonate lyase, and ketodeoxyuronate dehydrogenase in E. chrysanthemi.
利用R质粒pJB4JI通过Tn5诱变获得了缺乏多聚半乳糖醛酸分解代谢酶寡聚半乳糖醛酸裂解酶(Ogl-)和3-脱氧-D-甘油-2,5-己二酮糖酸(酮脱氧糖醛酸)脱氢酶(KduD-)的菊欧文氏菌EC16突变体。Ogl- Exu+(Exu+,D-半乳糖醛酸利用)和KduD- Exu-菌株能浸解马铃薯块茎组织并利用葡萄糖、甘油和葡萄糖酸盐,但它们不能利用多聚半乳糖醛酸、不饱和二半乳糖醛酸或饱和二半乳糖醛酸。遗传和物理证据表明,Ogl-突变体和一个KduD-重组体含有单拷贝的Tn5,且Tn5(卡那霉素抗性)与突变表型相关联。在Ogl+亲本中,甘油培养的细胞中存在基础水平的寡聚半乳糖醛酸裂解酶,饱和或不饱和二半乳糖醛酸存在时则存在诱导水平,而在类似条件下Ogl-菌株中检测不到寡聚半乳糖醛酸裂解酶。在Ogl-菌株中,3-脱氧-D-甘油-2,5-己二酮糖酸和不饱和二半乳糖醛酸的酶促产物可诱导果胶酸裂解酶、多聚半乳糖醛酸酶和酮脱氧糖醛酸脱氢酶,但二半乳糖醛酸不能诱导。KduD-菌株缺乏脱氢酶活性,但在二半乳糖醛酸存在时,产生的果胶酸裂解酶、多聚半乳糖醛酸酶和寡聚半乳糖醛酸裂解酶水平高于KduD+亲本。在KduD-菌株中,不饱和二半乳糖醛酸以“免费”方式诱导果胶酸裂解酶和寡聚半乳糖醛酸裂解酶,这表明诱导剂在细胞内积累。我们得出结论,酮脱氧糖醛酸途径的一种中间产物可诱导菊欧文氏菌中的果胶酸裂解酶、多聚半乳糖醛酸酶、寡聚半乳糖醛酸裂解酶和酮脱氧糖醛酸脱氢酶。