Saint C P, Ribbons D W
School of Pure and Applied Biology, University of Wales College of Cardiff, U.K.
FEMS Microbiol Lett. 1990 Jun 1;57(3):323-8. doi: 10.1016/0378-1097(90)90088-8.
Genes involved in 4-methyl-o-phthalate and 4-hydroxy-iso-phthalate catabolism reside on a 226-232 kbp catabolic plasmid termed MOP. This was confirmed by transformation and conjugation into an isogenic heat-cured (MOP-) derivative of the wild-type isolate, identified and termed Pseudomonas cepacia Pc701. Transformation confirmed the presence of Tn1 in MOP derived from Pc704, a mutant deficient in 4-methyl-o-phthalate catabolism. pCS1, a recombinant plasmid bearing MOP DNA, complemented MOP::Tn1 restoring the ability of Pc704 to grow on 4-methyl-o-phthalate. DNA-DNA hybridization using pCS1 as probe confirmed that loss of 4-methyl-o-phthalate catabolism by Pc704 was the result of Tn1 insertion into a 2.1 kbp HindIII fragment of MOP.
参与4-甲基邻苯二甲酸酯和4-羟基间苯二甲酸酯分解代谢的基因位于一个226 - 232 kbp的分解代谢质粒上,该质粒称为MOP。通过将其转化和接合到野生型菌株的同基因热治愈(MOP-)衍生物中得到证实,该衍生物被鉴定并命名为洋葱伯克霍尔德菌Pc701。转化证实了来自Pc704(一种4-甲基邻苯二甲酸酯分解代谢缺陷型突变体)的MOP中存在Tn1。携带MOP DNA的重组质粒pCS1补充了MOP::Tn1,恢复了Pc704在4-甲基邻苯二甲酸酯上生长的能力。以pCS1为探针的DNA-DNA杂交证实,Pc704丧失4-甲基邻苯二甲酸酯分解代谢能力是由于Tn1插入到MOP的一个2.1 kbp HindIII片段中所致。