<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY accession="ERP024232" alias="ena-STUDY-WDRC KAUST-24-07-2017-16:23:00:579-666" center_name="WDRC KAUST">
    <IDENTIFIERS>
      <PRIMARY_ID>ERP024232</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject">PRJEB21923</EXTERNAL_ID>
      <SUBMITTER_ID namespace="WDRC KAUST">ena-STUDY-WDRC KAUST-24-07-2017-16:23:00:579-666</SUBMITTER_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Two plasmids (i.e., blaCTX-M-15-positive and blaOXA-48-positive) were respectively fromKlebsiella pneumoniae L7 and Escherichia coli UPEC-RIY-4 bacteria. We sequenced the plasmid and assembled to several scaffords.</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Other"/>
      <STUDY_ABSTRACT>In this study, we evaluated the removal efficiency of these two kind of plasmids (i.e., blaCTX-M-15-positive and blaOXA-48-positive) by fouled and new membranes. To clean the mechanism of removal behavior, we tried to sequence and assemble the plasmids, and know about the size of these two kind of plasmids.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>Removal of antibiotic-resistant genes affected by varying extent of foulant on an anaerobic microfiltration membrane</CENTER_PROJECT_NAME>
      <STUDY_DESCRIPTION>In this study, we evaluated the removal efficiency of these two kind of plasmids (i.e., blaCTX-M-15-positive and blaOXA-48-positive) by fouled and new membranes. To clean the mechanism of removal behavior, we tried to sequence and assemble the plasmids, and know about the size of these two kind of plasmids.</STUDY_DESCRIPTION>
    </DESCRIPTOR>
    <STUDY_ATTRIBUTES>
      <STUDY_ATTRIBUTE>
        <TAG>ENA-FIRST-PUBLIC</TAG>
        <VALUE>2017-10-09</VALUE>
      </STUDY_ATTRIBUTE>
      <STUDY_ATTRIBUTE>
        <TAG>ENA-LAST-UPDATE</TAG>
        <VALUE>2017-07-25</VALUE>
      </STUDY_ATTRIBUTE>
    </STUDY_ATTRIBUTES>
  </STUDY>
</STUDY_SET>
