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. 2010 Dec 10;77(3):1086–1096. doi: 10.1128/AEM.01698-10

TABLE 3.

Detection of bacterial strains similar to M. petroleiphilum PM1 and catabolic genes encoding enzymes suggested to be involved in aerobic MTBE degradation in textiles from the microcosm experiments or directly from the pondsd

Culture or textile Detection of:
Length of fragment (bp)a Closest NCBI match Coverage (%) Maximum identity (%)
PM1 16S rRNA gene MdpA 1F/1R EthB for/for M/rev EthR for/rev M/rev
Reference pure cultures
    A. tertiaricarbonis L108 + 1,170 R. ruber IFP 2001 EthB 99 99
    R. ruber IFP 2001 + + 891 R. ruber IFP 2001 EthR 100 100
    M. petroleiphilum PM1 + + 684 M. petroleiphilum PM1 plasmid RPME01 MdpA 100 100
    Methylibium sp. strain R8 + + 659 M. petroleiphilum PM1 plasmid RPME01 MdpA 100 100
Microcosm expt textiles
    CO1 + + 1,049 R. ruber IFP 2007 EthB 100 99
    CO2 + + 1,164 R. ruber IFP 2001 EthB 99 99
    PO1 +b + 1,093 R. ruber IFP 2007 EthB 100 99
    PO2 +b + 1,021 R. zopfii IFP 2005 EthB 100 99
Environmental textilesc
    CO (150 cm) + + 1,026 R. ruber IFP 2001 EthB 99 100
    CO (420 cm) + + 1,053 R. ruber IFP 2001 EthB 99 99
    PO (150 cm) + + 1,166 R. ruber IFP 2001 EthB 99 99
    PO (420 cm) + + 901 R. ruber IFP 2007 EthB 100 100
a

Length of sequence obtained from the amplification product of the PCR assay (shown in boldface) used for BLAST analysis.

b

Successful sequencing; obtained fragment was 100% identical to Methylibium petroleiphilum PM1.

c

Environmental textiles were all sampled at 120 cm depth. The distance to inflow is given in parentheses.

d

See details in Table 1.