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Biodegradation of sodium benzoate by Pseudomonas biofilm consortium in a fluidized bed bioreactor

机译:假单胞菌生物膜联盟在流化床生物反应器中对苯甲酸钠的生物降解

摘要

Many strains of Gram-negative bacteria, such as Pseudomonas, are able to utilize audvariety of unusual chemicals, including a wide range or aromatic hydrocarbons and theirudderivatives for growth. Bacteria with the potential to degrade sodium benzoate wereudisolated, identified and grown as biofilms on sodium benzoate in a laboratory-scaleudfluidized bed biofilm bioreactor. Four Pseudomonas strains identified as P. aeruginosaud(BDS2) P. putida (BDS1 and GR1) and Burkholderia cepecia (GR3FAR) were used in audlaboratory-scale FBBR together with two Bacillus strains - Bacillus macroides (SBSY4)udand Bacillus simplex (MAR). Sodium benzoate biodegradation capacities of these speciesudwere compared under batch and continuous operations. Biofilm and planktonic bacterialudgrowth dynamics were monitored by plate counts, and optical density measurementsud(230nm) determined benzoate biodegradation. Overall, higher attached and planktonicudbacterial counts were determined under batch compared to continuous mode. In additionudto this, the ability of attached cells to use sodium benzoate as their sole carbon sourceudwas compared to their suspended counterparts in a batch system. There were moreudattached counts compared to suspended cells and attached cells apparently degradedudsodium benzoate better than planktonic cells. Similarly, higher rates of benzoateuddepletion were found to occur under batch compared to the continuous system. It thusudappeared that more cell growth implied more substrate consumption. SEM showedudattached cells and microcolonies of all the isolates on GAC, indicating their biofilmformingudabilities.
机译:许多革兰氏阴性菌菌株,例如假单胞菌,能够利用各种不寻常的化学物质,包括范围广泛的芳香烃或它们的衍生物,以进行生长。在实验室规模的流化床生物膜生物反应器中,将具有降解苯甲酸钠潜力的细菌分解,鉴定并作为苯甲酸钠上的生物膜生长。在实验室规模的FBBR中使用了四个鉴定为铜绿假单胞菌 ud(BD​​S2)恶臭假单胞菌(BDS1和GR1)和头皮伯克霍尔德氏菌(GR3FAR)的假单胞菌菌株以及两个芽孢杆菌菌株-大芽孢杆菌(SBSY4) ud和芽孢杆菌单纯形(MAR)。在分批和连续操作下比较了这些物种的苯甲酸钠生物降解能力。通过板数监测生物膜和浮游细菌的生长,并通过光密度测量(ud(230nm)来确定苯甲酸酯的生物降解。总体而言,与连续模式相比,分批测定的附着和浮游细菌数量更高。除此之外,与分批系统中悬浮细胞相比,附着细胞使用苯甲酸钠作为唯一碳源的能力。与悬浮细胞相比,有更多的未附着的计数,并且附着的细胞显然比浮游细胞更好地降解了的苯甲酸钠。类似地,与连续系统相比,批次下的苯甲酸盐/贫化率更高。因此似乎消失了,更多的细胞生长意味着更多的底物消耗。扫描电镜显示 GAC上所有分离株的未附着细胞和菌落,表明它们的生物膜形成能力。

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    Ntoampe Mannana Selina;

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  • 年度 2009
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