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一种用于分离氨氧化细菌的灭绝稀释法的评估改进。

An evaluated improvement of the extinction dilution method for isolation of ammonia-oxidizing bacteria.

作者信息

Aakra A, Utåker J B, Nes I F, Bakken L R

机构信息

Department of Chemistry and Biotechnology, Agricultural University of Norway, As.

出版信息

J Microbiol Methods. 1999 Dec;39(1):23-31. doi: 10.1016/s0167-7012(99)00094-9.

Abstract

An improved method for isolation of ammonia-oxidizing bacteria (AOB) by the extinction dilution technique is described. It is important to prevent the growth of heterotrophic organisms, which may easily outnumber the AOB in mixed cultures. This was achieved by careful elimination of C sources in the medium and by sealing the cultures from contact with the atmosphere, thus excluding air-borne, volatile compounds which support growth of heterotrophs. The sealing of the cultures reduced the number of heterotrophs by a factor of 10, thus grossly increasing the chances of obtaining pure AOB cultures. Another important factor is to use actively growing 'late log' cultures during the final isolation step. This was achieved by adjusting the buffer capacity to ensure a clearly visible pH indicator shift at a stage when one-third to one-half of the ammonia had been oxidized. By this improved isolation procedure, AOB were isolated from three different locations: an arable soil, a lead-contaminated soil and an animal house. For an unknown reason, several attempts to isolate pure cultures from a forest soil were unsuccessful, despite the presence of AOB in the primary extinction dilution cultures. The isolates from soils were all Nitrosospira spp. For isolation of AOB from the animal house, two growth media were used, one containing ammonium sulfate, and one containing urea. From the cultures with ammonium sulfate, Nitrosomonas spp. were isolated, whereas Nitrosospira spp. were isolated from the cultures with urea as the main ammonia source. The identifications of all isolates are based on morphology and 16S rDNA sequences.

摘要

本文描述了一种通过梯度稀释法改进的氨氧化细菌(AOB)分离方法。防止异养生物的生长很重要,因为在混合培养物中异养生物数量可能轻易超过AOB。这通过在培养基中仔细去除碳源以及密封培养物使其不与大气接触来实现,从而排除支持异养生物生长的空气传播的挥发性化合物。培养物的密封使异养生物数量减少了10倍,从而大大增加了获得纯AOB培养物的机会。另一个重要因素是在最终分离步骤中使用处于对数生长后期的活跃生长培养物。这通过调节缓冲能力来实现,以确保在三分之一到二分之一的氨被氧化时pH指示剂有明显可见的变化。通过这种改进的分离程序,从三个不同地点分离出了AOB:一种耕地土壤、一种铅污染土壤和一个动物饲养室。出于未知原因,尽管在初次梯度稀释培养物中存在AOB,但从森林土壤中分离纯培养物的几次尝试均未成功。从土壤中分离出的菌株均为亚硝化螺菌属。为了从动物饲养室分离AOB,使用了两种生长培养基,一种含有硫酸铵,另一种含有尿素。从以硫酸铵为培养基的培养物中分离出了亚硝化单胞菌属,而从以尿素为主要氨源的培养物中分离出了亚硝化螺菌属。所有分离菌株的鉴定均基于形态学和16S rDNA序列。

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