Mohn W W
Department of Microbiology and Immunology, University of British Columbia, Vancouver, Canada.
Appl Environ Microbiol. 1995 Jun;61(6):2145-50. doi: 10.1128/aem.61.6.2145-2150.1995.
Eleven isolates capable of growth on the resin acid dehydroabietic acid (DhA) were obtained from a sequencing batch reactor designed to treat a high-strength process stream from a paper mill. The isolates belonged to two groups, represented by strains DhA-33 and DhA-35, which were characterized. In the bioreactor, bacteria like DhA-35 were more abundant than those like DhA-33. The population in the bioreactor of organisms capable of growth on DhA was estimated to be 1.1 x 10(6) propagules per ml, based on a most-probable-number determination. Analysis of small-subunit rRNA partial sequences indicated that DhA-33 was most closely related to Sphingomonas yanoikuyae (Sab = 0.875) and that DhA-35 was most closely related to Zoogloea ramigera (Sab = 0.849). Both isolates additionally grew on other abietanes, i.e., abietic and palustric acids, but not on the pimaranes, pimaric and isopimaric acids. For DhA-33 and DhA-35 with DhA as the sole organic substrate, doubling times were 2.7 and 2.2 h, respectively, and growth yields were 0.30 and 0.25 g of protein per g of DhA, respectively. Glucose as a cosubstrate stimulated growth of DhA-33 on DhA and stimulated DhA degradation by the culture. Pyruvate as a cosubstrate did not stimulate growth of DhA-35 on DhA and reduced the specific rate of DhA degradation of the culture. DhA induced DhA and abietic acid degradation activities in both strains, and these activities were heat labile. Cell suspensions of both strains consumed DhA at a rate of 6 mumol mg of protein-1 h-1.(ABSTRACT TRUNCATED AT 250 WORDS)
从一个旨在处理造纸厂高强度工艺流的序批式反应器中获得了11株能够在树脂酸脱氢枞酸(DhA)上生长的分离株。这些分离株属于两组,以菌株DhA - 33和DhA - 35为代表,并对其进行了表征。在生物反应器中,像DhA - 35这样的细菌比像DhA - 33这样的细菌更丰富。基于最大可能数测定,生物反应器中能够在DhA上生长的生物群体估计为每毫升1.1×10⁶个繁殖体。小亚基rRNA部分序列分析表明,DhA - 33与矢野鞘氨醇单胞菌关系最密切(相似性 = 0.875),DhA - 35与枝状动胶菌关系最密切(相似性 = 0.849)。两种分离株还能在其他枞烷类化合物上生长,即枞酸和海松酸,但不能在半日花烷类化合物、海松酸和异海松酸上生长。以DhA为唯一有机底物时,DhA - 33和DhA - 35的倍增时间分别为2.7小时和2.2小时,生长产量分别为每克DhA产生0.30克和0.25克蛋白质。葡萄糖作为共底物刺激了DhA - 33在DhA上的生长,并刺激了培养物对DhA的降解。丙酮酸作为共底物没有刺激DhA - 35在DhA上的生长,反而降低了培养物对DhA的降解比速率。DhA诱导了两种菌株中DhA和枞酸的降解活性,且这些活性对热不稳定。两种菌株的细胞悬液以6 μmol毫克蛋白质⁻¹小时⁻¹的速率消耗DhA。(摘要截短至250字)