Kim Yong-Hak, Pak Kyungran, Pothuluri Jairaj V, Cerniglia Carl E
Division of Microbiology, National Center for Toxicological Research, US Food and Drug Administration, 3900 NCTR Rd., Jefferson, AR 72079, USA.
FEMS Microbiol Lett. 2004 May 1;234(1):169-75. doi: 10.1016/j.femsle.2004.03.027.
Mineralization of erythromycin A was studied using two differently (14)C-labeled erythromycins A, which were added to aquaculture sediment samples obtained from the two salmon hatchery sites in Washington state. The added erythromycin A did not significantly alter the numbers of the total viable colonies and erythromycin-resistant bacteria. Erythromycin-resistant Pseudomonas species contained a constitutive erythromycin esterase activity contributing to the inactivation of biologically active erythromycin A in aquatic and sediment environments. The initial rate of mineralization of erythromycin A appeared to be governed by the rate of release of soil-sorbed erythromycin A. After a prolonged lag time, the S-curves of erythromycin A mineralization were observed probably because of the increase in the population density metabolizing it. This study suggests that erythromycin A is partially or completely mineralized by the sediment microbial populations.
使用两种不同的(14)C标记的红霉素A研究了红霉素A的矿化作用,将其添加到从华盛顿州两个鲑鱼孵化场采集的水产养殖沉积物样本中。添加的红霉素A并未显著改变总活菌数和耐红霉素细菌的数量。耐红霉素假单胞菌含有组成型红霉素酯酶活性,有助于在水生和沉积物环境中使具有生物活性的红霉素A失活。红霉素A的初始矿化速率似乎受土壤吸附的红霉素A释放速率的控制。经过较长的滞后期后,观察到红霉素A矿化的S形曲线,这可能是因为代谢它的种群密度增加。这项研究表明,红霉素A被沉积物微生物群落部分或完全矿化。