Baoliang Jia, Bingquan Fan, Xinhua Sui, Mingbo Gong
Institute of Agricultural Resources and Regional Planning, Chinese Academy of Agricultural Sciences, Beijing 100081, China.
Wei Sheng Wu Xue Bao. 2008 Sep;48(9):1214-20.
To obtain pyrene-degrading microorganism strains, and to use them for bioremediation of polycyclic aromatic hydrocarbons-contaminated soil.
pyrene-degrading strains were isolated by agar plate subliming method. They were identified based on morphological observation, physiological and biochemical characteristics, and on analysis of their 16S rDNA gene sequence homology. Their ability to degrade PAHs in solid and liquid mineral salt medium, and in PAHs-contaminated soil, was studied by counting their live cells and measuring residual PAHs' quantity by HPLC.
Four pyrene-degrading strains TZh51, TZh52, TG42 and TG52 were isolated. The results indicated that TZh51's ability to degrade PAHs was stronger than the other three strains. TZh51 was identified as Mycobacterium sp.; however, it did not belong to the same species with the reported Mycobacterium sp. strain M11. Our results indicated that the effects on maximal pyrene-degrading quantity were incubation temperature at 35 degrees C and pyrene film thickness for 130 ng/mm2 when TZh51 was incubated on solid mineral salt medium coated with pyrene films. When TZh51 was incubated in liquid mineral salt medium containing 50 and 100 mg/L pyrene, 91.9% and 71.8% pyrene was degraded after 6 days. On the l0th day, maximal vital cells reached 2.0 x 10(8) and 6.0 x 10(8) cfu/mL, respectively. TZh51's ability to degrade pyrene was stronger than strain M11. Moreover, TZh51's vital cells reached 7.2 x 10(8) cfu/g dry soil on the 6th week and 91.4% phenanthrene, 86.9% fluoranthrene and 85.8% pyrene was degraded after 8 weeks, when both TZh51 and plants were used for bioremediation of PAHs-contaminated soil.
TZh51 had strong ability to degrade PAHs. In addition, combined bioremediation of TZh51 and plants was effective for PAHs-contaminated soil bioremediation.
获取芘降解微生物菌株,并将其用于多环芳烃污染土壤的生物修复。
采用琼脂平板升华法分离芘降解菌株。基于形态学观察、生理生化特性以及16S rDNA基因序列同源性分析对其进行鉴定。通过对活菌计数以及利用高效液相色谱法测定残留多环芳烃的量,研究它们在固体和液体矿物盐培养基以及多环芳烃污染土壤中降解多环芳烃的能力。
分离出四株芘降解菌株TZh51、TZh52、TG42和TG52。结果表明,TZh51降解多环芳烃的能力强于其他三株菌株。TZh51被鉴定为分枝杆菌属;然而,它与已报道的分枝杆菌属菌株M11不属于同一物种。我们的结果表明,当TZh51在涂有芘膜的固体矿物盐培养基上培养时,对芘最大降解量的影响因素为培养温度35℃和芘膜厚度130 ng/mm2。当TZh51在含有50和100 mg/L芘的液体矿物盐培养基中培养时,6天后芘的降解率分别为91.9%和71.8%。在第10天,最大活菌数分别达到2.0×10(8)和6.0×10(8) cfu/mL。TZh51降解芘的能力强于菌株M11。此外,当TZh51和植物同时用于多环芳烃污染土壤的生物修复时,第6周TZh51的活菌数达到7.2×10(8) cfu/g干土,8周后菲、荧蒽和芘的降解率分别为9l.4%、86.9%和85.8%。
TZh51具有较强的降解多环芳烃的能力。此外,TZh51与植物联合生物修复对多环芳烃污染土壤有效。