Palyzová Andrea, Zahradník Jiří, Marešová Helena, Sokolová Lucie, Kyslíková Eva, Grulich Michal, Štěpánek Václav, Řezanka Tomáš, Kyslík Pavel
Institute of Microbiology of the Czech Academy of Sciences, Vídeňská 1083, 14220, Prague 4, Czech Republic.
Department of Genetics and Microbiology, Faculty of Science, Charles University in Prague, Viničná 5, 12840, Prague 2, Czech Republic.
Folia Microbiol (Praha). 2018 May;63(3):273-282. doi: 10.1007/s12223-017-0563-2. Epub 2017 Nov 11.
The bacterial strain KDF8 capable of growth in the presence of diclofenac and codeine analgesics was obtained after chemical mutagenesis of nature isolates from polluted soils. The strain KDF8 was identified as Raoultella sp. based on its morphology, biochemical properties, and 16S rRNA gene sequence. It was deposited in the Czech Collection of Microorganisms under the number CCM 8678. A growing culture efficiently removed diclofenac (92% removal) and partially also codeine (about 30% degradation) from culture supernatants within 72 h at 28 °C. The degradation of six analgesics by the whole cell catalyst was investigated in detail. The maximum degradation of diclofenac (91%) by the catalyst was achieved at pH of 7 (1 g/L diclofenac). The specific removal rate at high concentrations of diclofenac and codeine increased up to 16.5 mg/g per h and 5.1 mg/g per h, respectively. HPLC analysis identified 4'-hydroxydiclofenac as a major metabolite of diclofenac transformation and 14-hydroxycodeinone as codeine transformation product. The analgesics ibuprofen and ketoprofen were also removed, albeit to a lower extent of 3.2 and 2.0 mg/g per h, respectively. Naproxen and mefenamic acid were not degraded.
通过对污染土壤中的天然分离菌株进行化学诱变,获得了能够在双氯芬酸和可待因镇痛药存在下生长的细菌菌株KDF8。基于其形态、生化特性和16S rRNA基因序列,菌株KDF8被鉴定为拉乌尔菌属(Raoultella sp.)。它以CCM 8678的编号保藏于捷克微生物菌种保藏中心。在28℃下,生长的培养物在72小时内有效地从培养上清液中去除了双氯芬酸(去除率92%),并且部分去除了可待因(约30%降解)。详细研究了全细胞催化剂对六种镇痛药的降解情况。在pH为7(双氯芬酸浓度为1 g/L)时,催化剂对双氯芬酸的最大降解率达到91%。在高浓度双氯芬酸和可待因条件下,比去除率分别提高到16.5 mg/g每小时和5.1 mg/g每小时。HPLC分析确定4'-羟基双氯芬酸是双氯芬酸转化的主要代谢产物,14-羟基可待因酮是可待因转化产物。镇痛药布洛芬和酮洛芬也被去除,尽管去除程度较低,分别为每小时3.2 mg/g和2.0 mg/g。萘普生和甲芬那酸未被降解。