<?xml version="1.0" encoding="UTF-8" standalone="yes"?>
<SAMPLE_SET>
    <SAMPLE accession="DRS002677" center_name="RYUKYU" alias="DRS002677">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00012484</PRIMARY_ID>
        </IDENTIFIERS>
        <TITLE>Rhodococcus corallinus strain B-276 (NSC)</TITLE>
        <SAMPLE_NAME>
            <TAXON_ID>36822</TAXON_ID>
            <SCIENTIFIC_NAME>Gordonia rubripertincta</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <DESCRIPTION>Bacteria and growth conditions: Cultures of R. corallinus B-276 (ATCC31338) were grown on Nutrient Broth No. 2 (Oxoid, Basingstoke, Hampshire, U.K.) containing 1% (w/v) glucose (NBG) at 30 °C with aerobic shaking (NSC). For the SC, propene and carbon were supplied via the gas phase with incubation in the NBG media at 30 °C. Cultures were grown either in shaking flasks or in sealed shaking flasks with propene (10%, v/v) supplied via the gas phase. Cells were harvested by centrifugation (8,000 × g for 10 min), washed twice with sterilized water, followed by re-centrifugation (8,000 × g for 10 min) to obtain cell pellets for DNA extraction. Cell pellets were stored at −80°C until use.</DESCRIPTION>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>B-276</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE accession="DRS002678" center_name="RYUKYU" alias="DRS002678">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00012485</PRIMARY_ID>
        </IDENTIFIERS>
        <TITLE>Rhodococcus corallinus strain B-276 (SC)</TITLE>
        <SAMPLE_NAME>
            <TAXON_ID>36822</TAXON_ID>
            <SCIENTIFIC_NAME>Gordonia rubripertincta</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <DESCRIPTION>Bacteria and growth conditions: Cultures of R. corallinus B-276 (ATCC31338) were grown on Nutrient Broth No. 2 (Oxoid, Basingstoke, Hampshire, U.K.) containing 1% (w/v) glucose (NBG) at 30 °C with aerobic shaking (NSC). For the SC, propene and carbon were supplied via the gas phase with incubation in the NBG media at 30 °C. Cultures were grown either in shaking flasks or in sealed shaking flasks with propene (10%, v/v) supplied via the gas phase. Cells were harvested by centrifugation (8,000 × g for 10 min), washed twice with sterilized water, followed by re-centrifugation (8,000 × g for 10 min) to obtain cell pellets for DNA extraction. Cell pellets were stored at −80°C until use.</DESCRIPTION>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>B-276</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
</SAMPLE_SET>
