首页> 外文期刊>Journal of industrial microbiology & biotechnology >High efficiency degradation of tetrahydrofuran (THF) using a membrane bioreactor: identification of THF-degrading cultures of Pseudonocardia sp. strain M1 and Rhodococcus ruber isolate M2
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High efficiency degradation of tetrahydrofuran (THF) using a membrane bioreactor: identification of THF-degrading cultures of Pseudonocardia sp. strain M1 and Rhodococcus ruber isolate M2

机译:使用膜生物反应器高效降解四氢呋喃(THF):鉴定假单胞菌(Pseudonocardia sp)的THF降解培养物。菌株M1和红球菌分离株M2

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摘要

A mixed microbial culture capable of growing aerobically on tetrahydrofuran (THF) as a sole carbon and energy source was used as the inoculum in a 10 l working volume membrane bioreactor. Following start-up, the reactor was operated in batch mode for 24 h and then switched to continuous feed with 100% biomass recycle. On average, greater than 96% of THF fed to the reactor was removed during the 8-month study. THF loading rates ranged from 0.62 to 9.07 g l~(–1) day~(–1) with a hydraulic retention time of 24 h. THF concentrations as high as 800 mg/l were tolerated by the culture. Biomass production averaged 0.28 kg total suspended solids/kg chemical oxygen demand removed, i.e., comparable to a conventional wastewater treatment process. Periodic batch wasting resulted in a solids retention time of 7–14 days. Reactor biomass typically ranged from 4 to 10 g/l volatile suspended solids and the effluent contained no solids. Pure THF-degrading cultures were isolated from the mixed culture based on morphological characteristics, Gram-staining and THF degradation. Based on 16S rDNA analysis the isolates were identified as Pseudonocardia sp. M1 and Rhodococcus ruber M2.
机译:将能够在四氢呋喃(THF)上作为唯一碳源和能源进行需氧生长的混合微生物培养物用作10升工作容积膜生物反应器中的接种物。启动后,反应器以分批模式运行24小时,然后切换到具有100%生物量循环的连续进料。在8个月的研究期间,平均除去了超过96%的进料到反应器中的THF。 THF的负载量范围为0.62至9.07 g l〜(-1)天〜(-1),水力停留时间为24 h。培养物可耐受高达800 mg / l的THF浓度。生物质生产平均悬浮总固体物质为0.28千克/除去的千克化学需氧量,即与常规废水处理工艺相当。定期分批浪费导致固体保留时间为7-14天。反应器生物质的挥发性悬浮固体含量通常为4至10 g / l,流出物不含固体。基于形态特征,革兰氏染色和THF降解,从混合培养物中分离出纯的THF降解培养物。根据16S rDNA分析,分离株被鉴定为假性心动过速。 M1和红球菌M2。

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