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<SAMPLE_SET>
    <SAMPLE alias="DRS200394" center_name="UTGSFSCB-ML" accession="DRS200394">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00019994</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>511145</TAXON_ID>
            <SCIENTIFIC_NAME>Escherichia coli str. K-12 substr. MG1655</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>The E. coli strain used was BHY173, a MG1655 derivative with mutations in restriction enzyme genes (genotype: MG1655 delta(mrr-hsdRMS-mcrB) deltamcrA). BHY187: BHY173(pACYC184deltatet).  This strain was grown in Lennox LB up to mid-exponential phase (O.D.600 =0.5) in two different batches. Then cells were harvested for RNA extraction. Total RNA was extracted from cell pellets using PureLink RNA mini kit (Ambion). rRNA was depleted using Ribo-Zero rRNA Removal kit (Gram-negative bacteria)(Epicentre). cDNA library for mRNA-seq was constructed using TruSeq RNA Sample Prep kit (Illumina). The indexed cDNA libraries were pooled and sequenced in HiSeq 2000 platform (Illumina).</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB3140</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>BHY187-1</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>BHY173</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>BHY187-1</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>genotype</TAG>
                <VALUE>MG1655 delta(mrr-hsdRMS-mcrB) deltamcrA</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE alias="DRS200395" center_name="UTGSFSCB-ML" accession="DRS200395">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00019995</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>511145</TAXON_ID>
            <SCIENTIFIC_NAME>Escherichia coli str. K-12 substr. MG1655</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>The E. coli strain used was BHY173, a MG1655 derivative with mutations in restriction enzyme genes (genotype: MG1655 delta(mrr-hsdRMS-mcrB) deltamcrA). BHY188: BHY173(pACYC184deltatet::dcm). This strain was grown in Lennox LB up to mid-exponential phase (O.D.600 =0.5) in two different batches. Then cells were harvested for RNA extraction. Total RNA was extracted from cell pellets using PureLink RNA mini kit (Ambion). rRNA was depleted using Ribo-Zero rRNA Removal kit (Gram-negative bacteria)(Epicentre). cDNA library for mRNA-seq was constructed using TruSeq RNA Sample Prep kit (Illumina). The indexed cDNA libraries were pooled and sequenced in HiSeq 2000 platform (Illumina).</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB3140</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>BHY188-1</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>BHY173</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>BHY188-1</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>genotype</TAG>
                <VALUE>MG1655 delta(mrr-hsdRMS-mcrB) deltamcrA</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE alias="DRS200396" center_name="UTGSFSCB-ML" accession="DRS200396">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00019996</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>511145</TAXON_ID>
            <SCIENTIFIC_NAME>Escherichia coli str. K-12 substr. MG1655</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>The E. coli strain used was BHY173, a MG1655 derivative with mutations in restriction enzyme genes (genotype: MG1655 delta(mrr-hsdRMS-mcrB) deltamcrA). BHY189: BHY173(pACYC184deltatet::ecoRIM). This strain was grown in Lennox LB up to mid-exponential phase (O.D.600 =0.5) in two different batches. Then cells were harvested for RNA extraction. Total RNA was extracted from cell pellets using PureLink RNA mini kit (Ambion). rRNA was depleted using Ribo-Zero rRNA Removal kit (Gram-negative bacteria)(Epicentre). cDNA library for mRNA-seq was constructed using TruSeq RNA Sample Prep kit (Illumina). The indexed cDNA libraries were pooled and sequenced in HiSeq 2000 platform (Illumina).</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB3140</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>BHY189-1</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>BHY173</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>BHY189-1</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>genotype</TAG>
                <VALUE>MG1655 delta(mrr-hsdRMS-mcrB) deltamcrA</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE alias="DRS200397" center_name="UTGSFSCB-ML" accession="DRS200397">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00019997</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>511145</TAXON_ID>
            <SCIENTIFIC_NAME>Escherichia coli str. K-12 substr. MG1655</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>The E. coli strain used was BHY173, a MG1655 derivative with mutations in restriction enzyme genes (genotype: MG1655 delta(mrr-hsdRMS-mcrB) deltamcrA). BHY193: BHY173(pACYC184deltatet::ecoP15Imod). This strain was grown in Lennox LB up to mid-exponential phase (O.D.600 =0.5) in two different batches. Then cells were harvested for RNA extraction. Total RNA was extracted from cell pellets using PureLink RNA mini kit (Ambion). rRNA was depleted using Ribo-Zero rRNA Removal kit (Gram-negative bacteria)(Epicentre). cDNA library for mRNA-seq was constructed using TruSeq RNA Sample Prep kit (Illumina). The indexed cDNA libraries were pooled and sequenced in HiSeq 2000 platform (Illumina).</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB3140</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>BHY193-1</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>BHY173</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>BHY193-1</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>genotype</TAG>
                <VALUE>MG1655 delta(mrr-hsdRMS-mcrB) deltamcrA</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE alias="DRS200398" center_name="UTGSFSCB-ML" accession="DRS200398">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00019998</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>511145</TAXON_ID>
            <SCIENTIFIC_NAME>Escherichia coli str. K-12 substr. MG1655</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>The E. coli strain used was BHY173, a MG1655 derivative with mutations in restriction enzyme genes (genotype: MG1655 delta(mrr-hsdRMS-mcrB) deltamcrA). BHY212: BHY173(pACYC184deltatet::ecoP1Imod). This strain was grown in Lennox LB up to mid-exponential phase (O.D.600 =0.5) in two different batches. Then cells were harvested for RNA extraction. Total RNA was extracted from cell pellets using PureLink RNA mini kit (Ambion). rRNA was depleted using Ribo-Zero rRNA Removal kit (Gram-negative bacteria)(Epicentre). cDNA library for mRNA-seq was constructed using TruSeq RNA Sample Prep kit (Illumina). The indexed cDNA libraries were pooled and sequenced in HiSeq 2000 platform (Illumina).</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB3140</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>BHY212-1</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>BHY173</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>BHY212-1</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>genotype</TAG>
                <VALUE>MG1655 delta(mrr-hsdRMS-mcrB) deltamcrA</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
</SAMPLE_SET>
