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从台湾养猪场废水处理系统中分离出的具有异养硝化能力的一株假单胞菌属细菌。

A strain of Pseudomonas sp. isolated from piggery wastewater treatment systems with heterotrophic nitrification capability in Taiwan.

作者信息

Su Jung-Jeng, Yeh Kuang-Sheng, Tseng Pin-Wei

机构信息

Division of Applied Biology, Animal Technology Institute Taiwan, Ding-Pu, Chunan, Miaoli, Taiwan, Republic of China.

出版信息

Curr Microbiol. 2006 Jul;53(1):77-81. doi: 10.1007/s00284-006-0021-x. Epub 2006 Jun 9.

DOI:10.1007/s00284-006-0021-x
PMID:16775792
Abstract

A high concentration of NH(4) (+) in piggery wastewater is major problem in Taiwan. Therefore, in our study, we isolated native heterotrophic nitrifiers for piggery wastewater treatment. Heterotrophic nitrifier AS-1 was isolated and characterized from the activated sludge of a piggery wastewater system. Sets of triplicate crimp-sealed serum bottles were used to demonstrate the heterotrophic nitrifying capability of strain AS-1 in an incubator at 30 degrees C. All serum bottles contained 80 mL medium, and the remainder of the bottle headspace was filled with pure oxygen. The experimental results showed that 2.5 +/- 0.2 mmol L(-1) NH(4) (+) was removed by 58 hours, and, eventually, 1.5 +/- 0.5 mmol L(-1) N(2) and 0.2 +/- 0.0 mmol L(-1) N(2)O were produced. The removal rate of NH(4) (+) by the strain AS-1 was 1.75 mmol NH(4) (+) g cell(-1) h(-1). This strain was then identified as Pseudomonas alcaligenes (97% identity) by sequencing its 16S rDNA and comparing it with other microorganisms. Thus, strain AS-1 displays high promise for future application for in situ NH(4) (+) removal from piggery wastewater.

摘要

养猪废水中高浓度的NH(4)(+)是台湾地区的一个主要问题。因此,在我们的研究中,我们分离出了用于处理养猪废水的本地异养硝化菌。异养硝化菌AS-1是从一个养猪废水系统的活性污泥中分离并鉴定出来的。使用了三组一式三份的压接密封血清瓶,在30摄氏度的培养箱中展示菌株AS-1的异养硝化能力。所有血清瓶都含有80 mL培养基,瓶顶空间的其余部分充满纯氧。实验结果表明,58小时内去除了2.5±0.2 mmol L(-1) NH(4)(+),最终产生了1.5±0.5 mmol L(-1) N(2)和0.2±0.0 mmol L(-1) N(2)O。菌株AS-1对NH(4)(+)的去除率为1.75 mmol NH(4)(+) g细胞(-1) h(-1)。通过对其16S rDNA进行测序并与其他微生物进行比较,该菌株随后被鉴定为产碱假单胞菌(同一性为97%)。因此,菌株AS-1在未来用于原位去除养猪废水中的NH(4)(+)方面具有很高的应用前景。

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J Appl Microbiol. 2001 Nov;91(5):853-60. doi: 10.1046/j.1365-2672.2001.01454.x.
7
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