<?xml version="1.0" encoding="UTF-8" standalone="yes"?>
<SAMPLE_SET>
    <SAMPLE alias="DRS056567" center_name="OKAYAMA" accession="DRS056567">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00024612</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>1577727</TAXON_ID>
            <SCIENTIFIC_NAME>Methylobacterium sp. MA-22A</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Methylobacterium sp. 22A was grown in 100-ml methanol medium prepared in 500-ml shaking flask. The media contain 0.5% methanol. For methanol, 30 micromolar Ca (Calcium chloride) was added. In log phase of the growth (OD600=0.3-0.4), the cells were harvested by centrifugation (9000 rpm, 4 C, 5 min), and frozen by liquid nitrogen. The cells were subjected to total RNA extraction with hot phenol extraction procedure (Babst et al., 1996, Mol Microbiol 19:827-839). Then ribosomal RNA was depleted by using Ribo-Zero rRNA removal kits (Gram-negative bacteria) (Epicentre) according to the manufacturer's protocol.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB3341</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>Methylobacterium_sp. 22A_RNAseq_Ca</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>MA-22A</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>Methylobacterium_sp. 22A_RNAseq_Ca</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE alias="DRS056568" center_name="OKAYAMA" accession="DRS056568">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00024613</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>1577727</TAXON_ID>
            <SCIENTIFIC_NAME>Methylobacterium sp. MA-22A</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Methylobacterium sp. 22A was grown in 100-ml methanol medium prepared in 500-ml shaking flask. The media contain 0.5% methanol. For methanol, 30 micromolar Ca (Calcium chloride) plus Ho (Holmium chloride) was added. In log phase of the growth (OD600=0.3-0.4), the cells were harvested by centrifugation (9000 rpm, 4 C, 5 min), and frozen by liquid nitrogen. The cells were subjected to total RNA extraction with hot phenol extraction procedure (Babst et al., 1996, Mol Microbiol 19:827-839). Then ribosomal RNA was depleted by using Ribo-Zero rRNA removal kits (Gram-negative bacteria) (Epicentre) according to the manufacturer's protocol.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB3341</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>Methylobacterium_sp. 22A_RNAseq_CaHo</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>MA-22A</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>Methylobacterium_sp. 22A_RNAseq_CaHo</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE alias="DRS056569" center_name="OKAYAMA" accession="DRS056569">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00024614</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>1577727</TAXON_ID>
            <SCIENTIFIC_NAME>Methylobacterium sp. MA-22A</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Methylobacterium sp. 22A was grown in 100-ml methanol medium prepared in 500-ml shaking flask. The media contain 0.5% methanol. For methanol, 30 micromolar Ca (Calcium chloride) plus La (Lanthanum chloride) was added. In log phase of the growth (OD600=0.3-0.4), the cells were harvested by centrifugation (9000 rpm, 4 C, 5 min), and frozen by liquid nitrogen. The cells were subjected to total RNA extraction with hot phenol extraction procedure (Babst et al., 1996, Mol Microbiol 19:827-839). Then ribosomal RNA was depleted by using Ribo-Zero rRNA removal kits (Gram-negative bacteria) (Epicentre) according to the manufacturer's protocol.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB3341</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>Methylobacterium_sp. 22A_RNAseq_CaLa</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>MA-22A</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>Methylobacterium_sp. 22A_RNAseq_CaLa</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE alias="DRS056570" center_name="OKAYAMA" accession="DRS056570">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00024615</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>1577727</TAXON_ID>
            <SCIENTIFIC_NAME>Methylobacterium sp. MA-22A</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Methylobacterium sp. 22A was grown in 100-ml methanol medium prepared in 500-ml shaking flask. The media contain 0.5% methanol. For methanol, 30 micromolar Ca (Calcium chloride) plus Lu (Lutetium chloride)  was added. In log phase of the growth (OD600=0.3-0.4), the cells were harvested by centrifugation (9000 rpm, 4 C, 5 min), and frozen by liquid nitrogen. The cells were subjected to total RNA extraction with hot phenol extraction procedure (Babst et al., 1996, Mol Microbiol 19:827-839). Then ribosomal RNA was depleted by using Ribo-Zero rRNA removal kits (Gram-negative bacteria) (Epicentre) according to the manufacturer's protocol.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB3341</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>Methylobacterium_sp. 22A_RNAseq_CaLu</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>MA-22A</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>Methylobacterium_sp. 22A_RNAseq_CaLu</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE alias="DRS056571" center_name="OKAYAMA" accession="DRS056571">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00024616</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>1577727</TAXON_ID>
            <SCIENTIFIC_NAME>Methylobacterium sp. MA-22A</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Methylobacterium sp. 22A was grown in 100-ml methanol medium prepared in 500-ml shaking flask. The media contain 0.5% methanol. For methanol, 30 micromolar La (Lanthanum chloride) was added. In log phase of the growth (OD600=0.3-0.4), the cells were harvested by centrifugation (9000 rpm, 4 C, 5 min), and frozen by liquid nitrogen. The cells were subjected to total RNA extraction with hot phenol extraction procedure (Babst et al., 1996, Mol Microbiol 19:827-839). Then ribosomal RNA was depleted by using Ribo-Zero rRNA removal kits (Gram-negative bacteria) (Epicentre) according to the manufacturer's protocol.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB3341</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>Methylobacterium_sp. 22A_RNAseq_La</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>MA-22A</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>Methylobacterium_sp. 22A_RNAseq_La</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE alias="DRS056572" center_name="OKAYAMA" accession="DRS056572">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00024617</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>1577727</TAXON_ID>
            <SCIENTIFIC_NAME>Methylobacterium sp. MA-22A</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Methylobacterium sp. 22A was grown in 100-ml methanol medium prepared in 500-ml shaking flask. The media contain 0.5% succinate. In log phase of the growth (OD600=0.3-0.4), the cells were harvested by centrifugation (9000 rpm, 4 C, 5 min), and frozen by liquid nitrogen. The cells were subjected to total RNA extraction with hot phenol extraction procedure (Babst et al., 1996, Mol Microbiol 19:827-839). Then ribosomal RNA was depleted by using Ribo-Zero rRNA removal kits (Gram-negative bacteria) (Epicentre) according to the manufacturer's protocol.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB3341</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>Methylobacterium_sp. 22A_RNAseq_S</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>MA-22A</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>Methylobacterium_sp. 22A_RNAseq_S</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
</SAMPLE_SET>
