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Isolation of bacteria able to grow on both polyethylene glycol (PEG) and polypropylene glycol (PPG) and their PEG/PPG dehydrogenases

机译:分离能够在聚乙二醇(PEG)和聚丙二醇(PPG)上生长的细菌及其PEG / PPG脱氢酶

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Two bacterial consortia growing on a random copolymer of ethylene glycol and propylene glycol units were obtained by enrichment cultures from various microbial samples. Six major strains included in both consortia were purified and identified as Sphingomonads, Pseudomonas sp. and Stenotrophomonas maltophilia. Three of them (Sphingobium sp. strain EK-1, Sphingopyxis macro-goltabida strain EY-1, and Pseudomonas sp. strain PE-2) utilized both PEG and polypropylene glycol (PPG) as a sole carbon source. Four PEG-utilizing bacteria had PEG dehydrogenase (PEG-DH) activity, which was induced by PEG. PCR products from DNA of these bacteria generated with primers designed from a PEG-DH gene (AB196775 for S. macrogoltabida strain 103) indicated the presence of a sequence that is the homologous to the PEG-DH gene (99% identity). On the other hand, five PPG-utilizing bacteria had PPG dehydrogenase (PPG-DH) activity, but the activity was constitutive. PCR of a PPG-DH gene was performed using primers designed from a polyvinyl alcohol dehydrogenase (PVA-DH) gene (AB190288 for Sphingomonas sp. strain 113P3) because a PPG-DH gene has not been cloned yet, but both PPG-DH and PVA-DH were active toward PPG and PVA (Mamoto et al. 2006). PCR products of the five strains did not have similarity to each other or to oxidoreductases including PVA-DH.
机译:通过从各种微生物样品中进行富集培养,获得了在乙二醇和丙二醇单元的无规共聚物上生长的两个细菌群落。纯化了两个财团中包括的六个主要菌株,并将其鉴定为Sphingomonads,假单胞菌属sp。和嗜麦芽窄食单胞菌。其中三个(鞘氨醇单胞菌菌株EK-1,Sphingopyxis macro-goltabida菌株EY-1和假单胞菌菌株PE-2)利用PEG和聚丙二醇(PPG)作为唯一碳源。四种利用PEG的细菌具有PEG脱氢酶(PEG-DH)活性,这是由PEG诱导的。用由PEG-DH基因设计的引物产生的这些细菌的DNA的PCR产物(针对S. macrogoltabida菌株103的AB196775)表明存在与PEG-DH基因同源的序列(99%同一性)。另一方面,五种利用PPG的细菌具有PPG脱氢酶(PPG-DH)活性,但该活性是组成性的。由于尚未克隆PPG-DH基因,但PPG-DH和PPG-DH和PPG-DH均被克隆,因此使用从聚乙烯醇脱氢酶(PVA-DH)基因(鞘氨醇单胞菌属菌株113P3的AB190288)设计的引物进行了PPG-DH基因的PCR。 PVA-DH对PPG和PVA具有活性(Mamoto等,2006)。这五个菌株的PCR产物彼此之间或与包括PVA-DH的氧化还原酶没有相似性。

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