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从序批式反应器中分离和鉴定异海松酸降解菌

Isolation and characterization of isopimaric acid-degrading bacteria from a sequencing batch reactor.

作者信息

Wilson A E, Moore E R, Mohn W W

机构信息

Department of Microbiology and Immunology, University of British Columbia, Vancouver, Canada.

出版信息

Appl Environ Microbiol. 1996 Sep;62(9):3146-51. doi: 10.1128/aem.62.9.3146-3151.1996.

Abstract

We isolated two aerobic, gram-negative bacteria which grew on the diterpene resin acid isopimaric acid (IpA) as the sole carbon source and electron donor. The source of the isolates was a sequencing batch reactor treating a high-strength process stream from a paper mill. The isolates, IpA-1 and IpA-2, also grew on pimaric and dehydroabietic acids, and IpA-1 grew on abietic acid. Both strains used fatty acids, but neither strain used camphor, sitosterol, or betulin. Strain IpA-1 grew anaerobically with nitrate as an electron acceptor. Strains IpA-1 and IpA-2 had growth yields of 0.19 and 0.23 g of protein per g of IpA, respectively. During growth, both strains transformed IpA carbon to approximately equal amounts of biomass, carbon dioxide, and dissolved organic carbon. In both strains, growth on IpA induced an enzymatic system which caused cell suspensions to transform all four of the above resin acids. Cell suspensions of IpA-1 and IpA-2 removed IpA at rates of 0.56 and 0.13 mumol mg of protein-1 h-1, respectively. Cultures and cell suspensions of both strains failed to completely consume pimaric acid and yielded small amounts of an apparent metabolite from this acid. Cultures and cell suspensions of both strains yielded large amounts of three apparent metabolites from dehydroabietic acid. Analysis of 16S rDNA sequences indicated that the isolates are distinct members of the genus Pseudomonas sensu stricto.

摘要

我们分离出了两种需氧革兰氏阴性菌,它们能以二萜树脂酸异海松酸(IpA)作为唯一碳源和电子供体生长。这些分离菌株源自一个序批式反应器,该反应器处理来自造纸厂的高强度工艺流。分离菌株IpA - 1和IpA - 2也能在海松酸和脱氢枞酸上生长,且IpA - 1能在枞酸上生长。两种菌株都利用脂肪酸,但均不利用樟脑、甾醇或桦木醇。菌株IpA - 1能以硝酸盐作为电子受体进行厌氧生长。菌株IpA - 1和IpA - 2每克IpA的生长产量分别为0.19克和0.23克蛋白质。在生长过程中,两种菌株都将IpA碳转化为大致等量的生物质、二氧化碳和溶解有机碳。在两种菌株中,在IpA上生长均诱导出一种酶系统,该系统使细胞悬液能转化上述所有四种树脂酸。IpA - 1和IpA - 2的细胞悬液去除IpA的速率分别为0.56和0.13 μmol mg蛋白质⁻¹ h⁻¹。两种菌株的培养物和细胞悬液均未能完全消耗海松酸,且从该酸中产生了少量明显的代谢产物。两种菌株的培养物和细胞悬液从脱氢枞酸中产生了大量三种明显的代谢产物。16S rDNA序列分析表明,这些分离菌株是狭义假单胞菌属的不同成员。

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Nucleic Acids Res. 1996 Jan 1;24(1):86-91. doi: 10.1093/nar/24.1.86.
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The Ribosomal Database Project (RDP).核糖体数据库项目(RDP)。
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