江西农业大学学报
江西農業大學學報
강서농업대학학보
ACTA AGRICULTURAE UNIVERSITATIS JIANGXIENSIS
2014年
6期
1357-1361
,共5页
多噬伯克霍尔德氏菌WS-FJ9%解有机磷机制%磷酸酶%定域%降解%优化
多噬伯剋霍爾德氏菌WS-FJ9%解有機燐機製%燐痠酶%定域%降解%優化
다서백극곽이덕씨균WS-FJ9%해유궤린궤제%린산매%정역%강해%우화
organophosphorus-degrading mechanism%phosphatase%localization%degradation%optimization
为研究多噬伯克霍尔德氏菌Burkholderia.multivorans WS-FJ9的解有机磷机制,对该菌磷酸酶产生的细胞定位进行了探讨并对其降解有机磷的营养条件进行了优化。采用冰浴超声破碎及液体培养的方法对WS-FJ9胞外、胞内及膜周质提取液的磷酸酶活性及不同营养条件下磷酸酶活性和解磷量分别进行了测定。结果表明:多噬伯克霍尔德氏菌Burkholderia.multivoransWS-FJ9能分泌酸性和碱性磷酸酶且以分泌酸性磷酸酶为主,均定域为胞外酶;该菌株解有机磷的最适碳、氮和磷源分别为葡萄糖、硫酸铵和卵磷脂,降解培养基中卵磷脂的最适浓度为0.5 g/L。研究结果为生物菌肥的开发与利用提供了理论参考依据,对可持续农业的发展具有重要意义。
為研究多噬伯剋霍爾德氏菌Burkholderia.multivorans WS-FJ9的解有機燐機製,對該菌燐痠酶產生的細胞定位進行瞭探討併對其降解有機燐的營養條件進行瞭優化。採用冰浴超聲破碎及液體培養的方法對WS-FJ9胞外、胞內及膜週質提取液的燐痠酶活性及不同營養條件下燐痠酶活性和解燐量分彆進行瞭測定。結果錶明:多噬伯剋霍爾德氏菌Burkholderia.multivoransWS-FJ9能分泌痠性和堿性燐痠酶且以分泌痠性燐痠酶為主,均定域為胞外酶;該菌株解有機燐的最適碳、氮和燐源分彆為葡萄糖、硫痠銨和卵燐脂,降解培養基中卵燐脂的最適濃度為0.5 g/L。研究結果為生物菌肥的開髮與利用提供瞭理論參攷依據,對可持續農業的髮展具有重要意義。
위연구다서백극곽이덕씨균Burkholderia.multivorans WS-FJ9적해유궤린궤제,대해균린산매산생적세포정위진행료탐토병대기강해유궤린적영양조건진행료우화。채용빙욕초성파쇄급액체배양적방법대WS-FJ9포외、포내급막주질제취액적린산매활성급불동영양조건하린산매활성화해린량분별진행료측정。결과표명:다서백극곽이덕씨균Burkholderia.multivoransWS-FJ9능분비산성화감성린산매차이분비산성린산매위주,균정역위포외매;해균주해유궤린적최괄탄、담화린원분별위포도당、류산안화란린지,강해배양기중란린지적최괄농도위0.5 g/L。연구결과위생물균비적개발여이용제공료이론삼고의거,대가지속농업적발전구유중요의의。
Phosphatase cellular localization was investigated and optimization of nutritional conditions was conducted for the purpose of studying the organophosphorus-degrading mechanism of Burkholderia multivorans WS-FJ9.The phosphatase activity of the extracellular,the intracellular and the membrane periplasm extracted solution,and both the phosphatase activity and organophosphorus-degrading quantity under different nutritional conditions were determined respectively using the methods of submerged culture and ice bath and ultrasonic breaking.The results showed that, B.multivorans WS-FJ9 was able to secrete acid phosphatase ( ACP ) and alkaline phosphatase ( AKP ) ,which were all localized as extracellular enzymes,and ACP was the principal component.The optimal carbon,nitrogen and phosphorus sources for degrading organophosphorus were glucose, ammonium sulfate and lecithin,respectively.The optimal concentration of lecithin was 0.5 g/L in the organophos?phorus-degrading culture medium.This study provides a theoretical reference basis for the development and utili?zation of bio-bacterial fertilizers,and is of great significance for the development of sustainable agriculture.