Basu Aditya, Phale Prashant S
Biotechnology group, School of Biosciences and Bioengineering, Indian Institute of Technology, Bombay, Powai, Mumbai 400 076, India.
Biodegradation. 2008 Feb;19(1):83-92. doi: 10.1007/s10532-007-9117-7. Epub 2007 May 9.
Pseudomonas putida CSV86 utilizes naphthalene (Nap), salicylate (Sal), benzyl alcohol (Balc), and methylnaphthalene (MN) preferentially over glucose. Methylnaphthalene is metabolized by ring-hydroxylation as well as side-chain hydroxylation pathway. Although the degradation property was found to be stable, the frequency of obtaining Nap(-)Sal(-)MN(-)Balc(-) phenotype increased to 11% in the presence of curing agents. This property was transferred by conjugation to Stenotrophomonas maltophilia CSV89 with a frequency of 7 x 10(-8) per donor cells. Transconjugants were Nap(+)Sal(+)MN(+)Balc(+) and metabolized MN by ring- as well as side-chain hydroxylation pathway. Transconjugants also showed the preferential utilization of aromatic compounds over glucose indicating transfer of the preferential degradation property. The transferred properties were lost completely when transconjugants were grown on glucose or 2YT. Attempts to detect and isolate plasmid DNA from CSV86 and transconjugants were unsuccessful. Transfer of degradation genes and its subsequent loss from the transconjugants was confirmed by PCR using primers specific for 1,2-dihydroxynaphthalene dioxygenase and catechol 2,3-dioxygenase (C23O) as well as by DNA-DNA hybridizations using total DNA as template and C23O PCR fragment as a probe. These results indicate the involvement of a probable conjugative element in the: (i) metabolism of aromatic compounds, (ii) ring- and side-chain hydroxylation pathways for MN, and (iii) preferential utilization of aromatics over glucose.
恶臭假单胞菌CSV86优先利用萘(Nap)、水杨酸(Sal)、苯甲醇(Balc)和甲基萘(MN)而非葡萄糖。甲基萘通过环羟基化以及侧链羟基化途径进行代谢。尽管发现其降解特性稳定,但在存在消除剂的情况下,获得Nap(-)Sal(-)MN(-)Balc(-)表型的频率增加到了11%。该特性通过接合转移到嗜麦芽窄食单胞菌CSV89,转移频率为每供体细胞7×10(-8)。转接合子为Nap(+)Sal(+)MN(+)Balc(+),并通过环羟基化以及侧链羟基化途径代谢MN。转接合子还表现出优先利用芳香族化合物而非葡萄糖,这表明优先降解特性发生了转移。当转接合子在葡萄糖或2YT上生长时,转移的特性完全丧失。从CSV86和转接合子中检测和分离质粒DNA的尝试均未成功。使用针对1,2 - 二羟基萘双加氧酶和儿茶酚2,3 - 双加氧酶(C23O)的特异性引物进行PCR,以及使用总DNA作为模板和C23O PCR片段作为探针进行DNA - DNA杂交,证实了降解基因的转移及其随后从转接合子中的丢失。这些结果表明可能存在一种接合元件参与:(i)芳香族化合物的代谢,(ii)MN的环羟基化和侧链羟基化途径,以及(iii)优先利用芳香族化合物而非葡萄糖。