<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hu M</submitter><funding>National Natural Science Foundation of China</funding><pagination>1135484</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9989019</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11</volume><pubmed_abstract>Lactate is the precursor for polylactide. In this study, a lactate producer of &lt;i>Z. mobilis&lt;/i> was constructed by replacing &lt;i>ZMO0038&lt;/i> with &lt;i>LmldhA&lt;/i> gene driven by a strong promoter P&lt;i>adhB&lt;/i>, replacing &lt;i>ZMO1650&lt;/i> with native &lt;i>pdc&lt;/i> gene driven by P&lt;i>tet,&lt;/i> and replacing native &lt;i>pdc&lt;/i> with another copy of &lt;i>LmldhA&lt;/i> driven by P&lt;i>adhB&lt;/i> to divert carbon from ethanol to D-lactate. The resultant strain ZML-pdc-ldh produced 13.8 ± 0.2 g/L lactate and 16.9 ± 0.3 g/L ethanol using 48 g/L glucose. Lactate production of ZML-pdc-ldh was further investigated after fermentation optimization in pH-controlled fermenters. ZML-pdc-ldh produced 24.2 ± 0.6 g/L lactate and 12.9 ± 0.8 g/L ethanol as well as 36.2 ± 1.0 g/L lactate and 40.3 ± 0.3 g/L ethanol, resulting in total carbon conversion rate of 98.3% ± 2.5% and 96.2% ± 0.1% with final product productivity of 1.9 ± 0.0 g/L/h and 2.2 ± 0.0 g/L/h in RMG5 and RMG12, respectively. Moreover, ZML-pdc-ldh produced 32.9 ± 0.1 g/L D-lactate and 27.7 ± 0.2 g/L ethanol as well as 42.8 ± 0.0 g/L D-lactate and 53.1 ± 0.7 g/L ethanol with 97.1% ± 0.0% and 99.1% ± 0.8% carbon conversion rate using 20% molasses or corncob residue hydrolysate, respectively. Our study thus demonstrated that it is effective for lactate production by fermentation condition optimization and metabolic engineering to strengthen heterologous &lt;i>ldh&lt;/i> expression while reducing the native ethanol production pathway. The capability of recombinant lactate-producer of &lt;i>Z. mobilis&lt;/i> for efficient waste feedstock conversion makes it a promising biorefinery platform for carbon-neutral biochemical production.</pubmed_abstract><journal>Frontiers in bioengineering and biotechnology</journal><pubmed_title>Metabolic engineering of &lt;i>Zymomonas mobilis&lt;/i> for co-production of D-lactic acid and ethanol using waste feedstocks of molasses and corncob residue hydrolysate.</pubmed_title><pmcid>PMC9989019</pmcid><funding_grant_id>21978071 U1932141</funding_grant_id><pubmed_authors>Yang X</pubmed_authors><pubmed_authors>Xu P</pubmed_authors><pubmed_authors>Hu W</pubmed_authors><pubmed_authors>Hu M</pubmed_authors><pubmed_authors>Bao W</pubmed_authors><pubmed_authors>Peng Q</pubmed_authors><pubmed_authors>Xiang Y</pubmed_authors><pubmed_authors>He Q</pubmed_authors><pubmed_authors>Yan X</pubmed_authors><pubmed_authors>Yang S</pubmed_authors><pubmed_authors>Li M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Metabolic engineering of &lt;i>Zymomonas mobilis&lt;/i> for co-production of D-lactic acid and ethanol using waste feedstocks of molasses and corncob residue hydrolysate.</name><description>Lactate is the precursor for polylactide. In this study, a lactate producer of &lt;i>Z. mobilis&lt;/i> was constructed by replacing &lt;i>ZMO0038&lt;/i> with &lt;i>LmldhA&lt;/i> gene driven by a strong promoter P&lt;i>adhB&lt;/i>, replacing &lt;i>ZMO1650&lt;/i> with native &lt;i>pdc&lt;/i> gene driven by P&lt;i>tet,&lt;/i> and replacing native &lt;i>pdc&lt;/i> with another copy of &lt;i>LmldhA&lt;/i> driven by P&lt;i>adhB&lt;/i> to divert carbon from ethanol to D-lactate. The resultant strain ZML-pdc-ldh produced 13.8 ± 0.2 g/L lactate and 16.9 ± 0.3 g/L ethanol using 48 g/L glucose. Lactate production of ZML-pdc-ldh was further investigated after fermentation optimization in pH-controlled fermenters. ZML-pdc-ldh produced 24.2 ± 0.6 g/L lactate and 12.9 ± 0.8 g/L ethanol as well as 36.2 ± 1.0 g/L lactate and 40.3 ± 0.3 g/L ethanol, resulting in total carbon conversion rate of 98.3% ± 2.5% and 96.2% ± 0.1% with final product productivity of 1.9 ± 0.0 g/L/h and 2.2 ± 0.0 g/L/h in RMG5 and RMG12, respectively. Moreover, ZML-pdc-ldh produced 32.9 ± 0.1 g/L D-lactate and 27.7 ± 0.2 g/L ethanol as well as 42.8 ± 0.0 g/L D-lactate and 53.1 ± 0.7 g/L ethanol with 97.1% ± 0.0% and 99.1% ± 0.8% carbon conversion rate using 20% molasses or corncob residue hydrolysate, respectively. Our study thus demonstrated that it is effective for lactate production by fermentation condition optimization and metabolic engineering to strengthen heterologous &lt;i>ldh&lt;/i> expression while reducing the native ethanol production pathway. The capability of recombinant lactate-producer of &lt;i>Z. mobilis&lt;/i> for efficient waste feedstock conversion makes it a promising biorefinery platform for carbon-neutral biochemical production.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2026-06-23T03:13:13.065Z</modification><creation>2025-04-19T16:26:27.704Z</creation></dates><accession>S-EPMC9989019</accession><cross_references><pubmed>36896016</pubmed><doi>10.3389/fbioe.2023.1135484</doi></cross_references></HashMap>