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  <identifier identifierType="DOI">10.18453/rosdok_id00002565</identifier>
  <creators>
    <creator>
      <creatorName nameType="Personal">Song, Shanshan</creatorName>
      <givenName>Shanshan</givenName>
      <familyName>Song</familyName>
      <nameIdentifier nameIdentifierScheme="GND" schemeURI="http://d-nb.info/gnd/">http://d-nb.info/gnd/1201001684</nameIdentifier>
    </creator>
  </creators>
  <titles>
    <title>Engineering formate assimilation in Synechocystis sp. PCC 6803</title>
  </titles>
  <publisher>Universität Rostock</publisher>
  <publicationYear>2019</publicationYear>
  <resourceType resourceTypeGeneral="Text" />
  <subjects>
    <subject xml:lang="en" schemeURI="http://dewey.info/" subjectScheme="dewey">570 Life science</subject>
  </subjects>
  <dates>
    <date dateType="Created">2019</date>
  </dates>
  <language>en</language>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="PURL">http://purl.uni-rostock.de/rosdok/id00002565</alternateIdentifier>
    <alternateIdentifier alternateIdentifierType="URN">urn:nbn:de:gbv:28-rosdok_id00002565-6</alternateIdentifier>
  </alternateIdentifiers>
  <descriptions>
    <description descriptionType="Abstract">To improve photosynthetic efficiency, a synthetic formate assimilation (FA) pathway is designed in this study to function as an additional carbon-fixing route, which possibly also reduce the photorespiratory loss of CO2 via the inhibition of glycine decarboxylation. To establish FA, genes encoding the proteins 10-formyl-THF ligase (FTL), 5,10-methylene-THF dehydrogenase (MtdA), and 5,10-methenyl-THF cyclohydrolase (FchA) from M. extorquens AM1 were transferred into the model cyanobacterium Synechocystis sp. PCC 6803.</description>
  </descriptions>
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