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Our previous work demonstrated the bifunctional activity of chlamydial DapF\n            <jats:italic>in vitro<\/jats:italic>\n            and in a heterologous system (\n            <jats:named-content content-type=\"genus-species\">Escherichia coli<\/jats:named-content>\n            ). In the present study, we employed a substrate competition strategy to demonstrate DapF\n            <jats:italic>\n              <jats:sub>Ct<\/jats:sub>\n            <\/jats:italic>\n            function\n            <jats:italic>in vivo<\/jats:italic>\n            in\n            <jats:named-content content-type=\"genus-species\">C. trachomatis<\/jats:named-content>\n            .\n          <\/jats:p>","DOI":"10.1128\/iai.00401-20","type":"journal-article","created":{"date-parts":[[2020,10,27]],"date-time":"2020-10-27T14:32:27Z","timestamp":1603809147000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":1,"title":["Competing Substrates for the Bifunctional Diaminopimelic Acid Epimerase\/Glutamate Racemase Modulate Peptidoglycan Synthesis in Chlamydia 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