江苏科技大学学报(自然科学版)
江囌科技大學學報(自然科學版)
강소과기대학학보(자연과학판)
Journal of Jiangsu University of Science and Technology(Natural Science Edition)
2015年
5期
501-506
,共6页
马娟%杨芬%唐玉斌%陈芳艳%王新刚
馬娟%楊芬%唐玉斌%陳芳豔%王新剛
마연%양분%당옥빈%진방염%왕신강
壬基酚%生物降解%降解条件优化%施氏假单胞菌%非脱羧勒克菌%16SrDNA
壬基酚%生物降解%降解條件優化%施氏假單胞菌%非脫羧勒剋菌%16SrDNA
임기분%생물강해%강해조건우화%시씨가단포균%비탈최륵극균%16SrDNA
nonylPhenol%biodegradation%optimization of degradation conditions%Pseudomonas stutzeri%Leclercia
为了有效地对壬基酚( NP)污染水环境进行生物修复,丰富高效降解NP的微生物资源,从垃圾填埋场的垃圾渗滤液中,分离得到两株NP高效降解菌SLY7和SLY8,根据菌落的形态特征和16S rDNA序列分析,初步鉴定SLY7为施氏假单胞菌( Pseudomonas stutzeri) ,SLY8为非脱羧勒克菌( Leclercia adecarboxylata) .通过摇瓶实验考察NP的初始浓度、pH、温度以及投菌量等因素对菌株降解NP能力的影响.结果表明:菌株SLY7的最佳降解条件为温度30℃,pH为8.0,接种量3%( V/V),振荡速率120 r/min,在此条件下,历时3 d,对初始浓度为10 mg/L的NP的降解率可达72.83%;菌株SLY8的最佳降解条件为温度35℃,pH为7.0,接种量5%(V/V),振荡速率120 r/min,在此条件下,历时3 d,对初始浓度为5 mg/L的NP的降解率可达64.43%.
為瞭有效地對壬基酚( NP)汙染水環境進行生物脩複,豐富高效降解NP的微生物資源,從垃圾填埋場的垃圾滲濾液中,分離得到兩株NP高效降解菌SLY7和SLY8,根據菌落的形態特徵和16S rDNA序列分析,初步鑒定SLY7為施氏假單胞菌( Pseudomonas stutzeri) ,SLY8為非脫羧勒剋菌( Leclercia adecarboxylata) .通過搖瓶實驗攷察NP的初始濃度、pH、溫度以及投菌量等因素對菌株降解NP能力的影響.結果錶明:菌株SLY7的最佳降解條件為溫度30℃,pH為8.0,接種量3%( V/V),振盪速率120 r/min,在此條件下,歷時3 d,對初始濃度為10 mg/L的NP的降解率可達72.83%;菌株SLY8的最佳降解條件為溫度35℃,pH為7.0,接種量5%(V/V),振盪速率120 r/min,在此條件下,歷時3 d,對初始濃度為5 mg/L的NP的降解率可達64.43%.
위료유효지대임기분( NP)오염수배경진행생물수복,봉부고효강해NP적미생물자원,종랄급전매장적랄급삼려액중,분리득도량주NP고효강해균SLY7화SLY8,근거균락적형태특정화16S rDNA서렬분석,초보감정SLY7위시씨가단포균( Pseudomonas stutzeri) ,SLY8위비탈최륵극균( Leclercia adecarboxylata) .통과요병실험고찰NP적초시농도、pH、온도이급투균량등인소대균주강해NP능력적영향.결과표명:균주SLY7적최가강해조건위온도30℃,pH위8.0,접충량3%( V/V),진탕속솔120 r/min,재차조건하,력시3 d,대초시농도위10 mg/L적NP적강해솔가체72.83%;균주SLY8적최가강해조건위온도35℃,pH위7.0,접충량5%(V/V),진탕속솔120 r/min,재차조건하,력시3 d,대초시농도위5 mg/L적NP적강해솔가체64.43%.
In order to effectively control the NP-polluted water and enrich microbial resources of NP-degrading bacteria, two bacterial strains were isolated from the landfill leachate.The two NP-degrading bacteria, designat-ed strains SLY7 and SLY8.The morphology observation and 16S rDNA identification revealed that the two strains belonged to Pseudomonas stutzeri and Leclercia adecarboxylata, respectively.By shaking flasks tests, the effects of the conditions of degradation of NP by the strains was studied.SLY7 was determined that the optimum condi-tions were inoculum amount 3%, pH 8.0, and 30℃, on a shaker at 120 rpm for 3 d.Under these conditions, when the initial concentration was 10 mg/L, the degrading rate of NP reached 72.83%.SLY8 was determined that the optimum conditions were inoculum amount 5%, pH 7.0, and 35℃, on a shaker at 120 rpm.Under these conditions, the duration was 3 d, when the initial concentration was 5 mg/L, the degrading rate of NP reached 64.43%.