<?xml version="1.0" encoding="UTF-8"?>
<SAMPLE_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <SAMPLE center_name="UMH-EGG" alias="Santa Pola Solar Saltern Metagenome Sample SS19" accession="SRS255950">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS255950</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00704054</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>Santa Pola Solar Saltern Metagenome Sample SS19</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>496920</TAXON_ID>
      <SCIENTIFIC_NAME>saltern metagenome</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>The sample was collected  from Bras del Port salterns in Alicante, Spain . The concentrator pond (SS19) was sampled on July 21, 2008. The salinity was measured using a hand refractometer (salinity 19%). The sample was sequentially filtered through a 5 micron and 0.22 micron-pore size polycarbonate filters using a peristaltic pump.  Filters were stored at -80 deg C until DNA extraction. DNA was extracted as described before (Martin-Cuadrado et al, 2007), briefly, filters were thawed on ice and then treated with 1 mg/ml lysozyme and 0.2 mg/ml proteinase K (final concentrations). Nucleic acids were extracted with phenol/chloroform/isoamyl alcohol and chloroform/isoamyl alcohol and DNA integrity was checked by agarose gel electrophoresis. 5 micrograms of DNA sent separately for sequencing (Roche 454 GS-FLX system, Titanium chemistry, by GATC, Konstanz, Germany) (one full plate 454).</DESCRIPTION>
  </SAMPLE>
  <SAMPLE center_name="UMH-EGG" alias="Santa Pola Solar Saltern Metagenome Sample SS37" accession="SRS255951">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS255951</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00704055</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>Santa Pola Solar Saltern Metagenome Sample SS37</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>496920</TAXON_ID>
      <SCIENTIFIC_NAME>saltern metagenome</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>The sample was collected  from Bras del Port salterns in Alicante, Spain . The concentrator pond (SS19) was sampled on July 21, 2008. The salinity was measured using a hand refractometer (salinity 19%). The sample was sequentially filtered through a 5 micron and 0.22 micron-pore size polycarbonate filters using a peristaltic pump.  Filters were stored at -80 deg C until DNA extraction. DNA was extracted as described before (Martin-Cuadrado et al, 2007), briefly, filters were thawed on ice and then treated with 1 mg/ml lysozyme and 0.2 mg/ml proteinase K (final concentrations). Nucleic acids were extracted with phenol/chloroform/isoamyl alcohol and chloroform/isoamyl alcohol and DNA integrity was checked by agarose gel electrophoresis. 5 micrograms of DNA sent separately for sequencing (Roche 454 GS-FLX system, Titanium chemistry, by GATC, Konstanz, Germany) (one full plate 454).</DESCRIPTION>
  </SAMPLE>
</SAMPLE_SET>
