Topp E, Crawford R L, Hanson R S
Gray Freshwater Biological Institute, University of Minnesota, Navarre 55392.
Appl Environ Microbiol. 1988 Oct;54(10):2452-9. doi: 10.1128/aem.54.10.2452-2459.1988.
The influence of high concentrations of pentachlorophenol (PCP) and readily metabolizable carbon on the activity and viability of a PCP-degrading Flavobacterium sp. was examined in a mineral salts medium. Lags preceding PCP removal by glutamate-grown Flavobacterium cells were greatly attenuated by the addition of glutamate, aspartate, succinate, acetate, glucose, or cellobiose. The effect of these supplementary carbon sources on the apparent lag was not mediated entirely through the stimulation of growth since PCP metabolism accompanied the onset of growth. The specific activity of PCP-degrading cells in the absence of supplementary carbon was 1.51 x 10(-13) +/- 0.08 x 10(-13) g of PCP per cell per h and in the presence of supplementary carbon was 0.92 x 10(-13) +/- 0.09 x 10(-13) g of PCP per cell per h. Glutamate in combination with glucose or cellobiose partially repressed PCP metabolism. PCP removal by PCP-induced, glutamate-grown cells suspended in the presence of 4 g of sodium glutamate per liter was sensitive to shock loads of PCP, with a Ki of about 86.8 micrograms/ml. Subsequent removal rates, however, were more resistant to PCP. Optimal stimulation of PCP removal by sodium glutamate required 3.0 g/liter, about the same concentration as that which saturated growth in the absence of PCP. PCP removal rates decayed within minutes following the transfer of PCP-induced, glutamate-grown cells to media containing PCP without supplementary carbon, and increasing PCP concentrations accelerated the decay.(ABSTRACT TRUNCATED AT 250 WORDS)
在无机盐培养基中,研究了高浓度五氯苯酚(PCP)和易代谢碳对一株降解PCP的黄杆菌属细菌活性和生存能力的影响。添加谷氨酸、天冬氨酸、琥珀酸、乙酸、葡萄糖或纤维二糖可大大缩短谷氨酸培养的黄杆菌细胞去除PCP之前的停滞期。这些补充碳源对表观停滞期的影响并非完全通过刺激生长介导,因为PCP代谢伴随生长开始。在无补充碳的情况下,降解PCP细胞的比活性为每细胞每小时1.51×10⁻¹³±0.08×10⁻¹³克PCP,在有补充碳的情况下为每细胞每小时0.92×10⁻¹³±0.09×10⁻¹³克PCP。谷氨酸与葡萄糖或纤维二糖组合可部分抑制PCP代谢。悬浮于每升含4克谷氨酸钠中的PCP诱导的、谷氨酸培养的细胞对PCP冲击负荷敏感,其半数抑制浓度(Ki)约为86.8微克/毫升。然而,随后的去除率对PCP更具抗性。谷氨酸钠对PCP去除的最佳刺激需要3.0克/升,这与在无PCP时使生长饱和的浓度大致相同。将PCP诱导的、谷氨酸培养的细胞转移至不含补充碳的含PCP培养基后,PCP去除率在数分钟内下降,PCP浓度增加会加速这种下降。(摘要截短于250字)