Thorenoor Nithyananda, Kim Yong-Hak, Lee Cheolju, Yu Myeong-Hee, Engesser Karl-Heinrich
Life Sciences Division, Korea Institute of Science and Technology, Seongbuk, Seoul 136-791, Republic of Korea.
Chemosphere. 2009 Jun;75(10):1287-93. doi: 10.1016/j.chemosphere.2009.03.032. Epub 2009 Apr 16.
A previously uncultured Propionibacterium was isolated from a highly diluted sample (10(-6)mL) of activated sludge of paper mill effluent. The isolate MOB600 was able to grow on anisole, phenetole, benzene, toluene, phenol, styrene and biphenyl, although it used only limited carbon sources in the minimal media. The partial DNA sequence of 16S ribosomal RNA gene was 93% identical to Luteococcus peritoni CCUG38120 as the closest neighborhood in the family Propionibacteriaceae. Strain MOB600 produced 2-methoxyphenol and 2-ethoxyphenol seemingly in an unproductive pathway from the degradation of anisole and phenetole, respectively. It had a substrate preference to favor 3-alkoxyphenols over 2-alkoxyphenols. Formation of 3-hydroxylated O-aryl alkyl ether was substantially proved by the nearly 1:1 biotransformation of substrate-analogous 1,2-methylenedioxybenzene to 3,4-methylenedioxyphenol (sesamol) showing end-product inhibition. The strain converted 2-/3-methoxyphenols to 3-methoxycatechol. The extradiol ring fission of 3-methoxycatechol appeared to take place in the production of a yellow-colored 2-hydroxymuconate derivative, thereby being able to release methanol spontaneously. High specificity polymerase chain reaction screening for bacterial dioxygenases revealed that the genomic DNA encoded at least three ring-hydroxylating dioxygenase large subunits. Being consistent with substrate availability for this strain, the obtained sequences were closely related to large subunits of an isopropylbenzene 2,3-dioxygenase, a benzene 1,2-dioxygenase, a biphenyl 2,3-dioxygenase, a benzoate 1,2-dioxygenase and a putative dioxygenase in Rhodococcus strains. Our results demonstrate that strain MOB600 may play a major role in the degradation of lignin-like O-aryl alkyl ethers and various aromatic hydrocarbon pollutants in activated sludge of paper mill effluent.
从造纸厂废水活性污泥的高稀释样本(10⁻⁶ mL)中分离出一种先前未培养过的丙酸杆菌。分离菌株MOB600能够在苯甲醚、苯乙醚、苯、甲苯、苯酚、苯乙烯和联苯上生长,尽管它在基本培养基中仅利用有限的碳源。16S核糖体RNA基因的部分DNA序列与丙酸杆菌科中最近邻的腹膜黄体球菌CCUG38120有93%的同一性。菌株MOB600分别从苯甲醚和苯乙醚的降解中以看似无生产性的途径产生了2 - 甲氧基苯酚和2 - 乙氧基苯酚。它对3 - 烷氧基苯酚的底物偏好高于2 - 烷氧基苯酚。通过底物类似物1,2 - 亚甲基二氧基苯几乎1:1生物转化为3,4 - 亚甲基二氧基苯酚(芝麻酚)并显示终产物抑制,充分证明了3 - 羟基化O - 芳基烷基醚的形成。该菌株将2 - /3 - 甲氧基苯酚转化为3 - 甲氧基儿茶酚。3 - 甲氧基儿茶酚的间位二醇环裂解似乎发生在产生黄色的2 - 羟基粘康酸衍生物的过程中,从而能够自发释放甲醇。对细菌双加氧酶的高特异性聚合酶链反应筛选表明,基因组DNA编码至少三个环羟基化双加氧酶大亚基。与该菌株的底物可用性一致,获得的序列与异丙苯2,3 - 双加氧酶、苯1,2 - 双加氧酶、联苯2,3 - 双加氧酶、苯甲酸1,2 - 双加氧酶以及红球菌菌株中的一种推定双加氧酶的大亚基密切相关。我们的结果表明,菌株MOB600可能在造纸厂废水活性污泥中木质素样O - 芳基烷基醚和各种芳烃污染物的降解中起主要作用。