Akhmetov L I, Filonov A E, Puntus I F, Kosheleva I A, Nechaeva I A, Yonge D R, Petersen J N, Boronin A M
Mikrobiologiia. 2008 Jan-Feb;77(1):29-39.
The process of naphthalene degradation by indigenous, introduced, and transconjugant strains was studied in laboratory soil microcosms. Conjugation transfer of catabolic plasmids was demonstrated in naphthalene-contaminated soil. Both indigenous microorganisms and an introduced laboratory strain BS394 (pNF142::TnMod-OTc) served as donors of these plasmids. The indigenous bacterial degraders of naphthalene isolated from soil were identified as Pseudomonas putida and Pseudomonas fluorescens. The frequency of plasmid transfer in soil was 10(-5)-10(-4) per donor cell. The activity of the key enzymes of naphthalene biodegradation in indigenous and transconjugant strains was studied. Transconjugant strains harboring indigenous catabolic plasmids possessed high salicylate hydroxylase and low catechol-2,3-dioxygenase activities, in contrast to indigenous degraders, which had a high level of catechol-2,3-dioxygenase activity and a low level of salicylate hydroxylase. Naphthalene degradation in batch culture in liquid mineral medium was shown to accelerate due to cooperation of the indigenous naphthalene degrader P. fluorescens AP1 and the transconjugant strain P. putida KT2442 harboring the indigenous catabolic plasmid pAP35. The role of conjugative transfer of naphthalene biodegradation plasmids in acceleration of naphthalene degradation was demonstrated in laboratory soil microcosms.
在实验室土壤微观系统中研究了本地菌株、引入菌株和转接合子菌株对萘的降解过程。在萘污染土壤中证实了分解代谢质粒的接合转移。本地微生物和引入的实验室菌株BS394(pNF142::TnMod-OTc)均作为这些质粒的供体。从土壤中分离出的萘的本地细菌降解菌被鉴定为恶臭假单胞菌和荧光假单胞菌。土壤中质粒转移的频率为每个供体细胞10^(-5)-10^(-4)。研究了本地菌株和转接合子菌株中萘生物降解关键酶的活性。与具有高水平儿茶酚-2,3-双加氧酶活性和低水平水杨酸羟化酶活性的本地降解菌相比,携带本地分解代谢质粒的转接合子菌株具有高水杨酸羟化酶活性和低儿茶酚-2,3-双加氧酶活性。在液体矿物培养基的分批培养中,由于本地萘降解菌荧光假单胞菌AP1与携带本地分解代谢质粒pAP35的转接合子菌株恶臭假单胞菌KT2442的合作,萘的降解加速。在实验室土壤微观系统中证明了萘生物降解质粒的接合转移在加速萘降解中的作用。