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                <identifier>oai:data.mendeley.com/n9jkwkrf4d.1</identifier>
                <datestamp>2024-05-28T08:29:38Z</datestamp>
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            <metadata><oai_dc:dc xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
    <dc:creator id="https://orcid.org/0009-0005-7679-9482">Waldschitz, Daniel</dc:creator>
    <dc:title>Bioprocess valorization of spent sulfite liquor with Corynebacterium glutamicum on minimal medium</dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>Fermentation data of 5 replicate batch cultivations with Corynebacterium glutamicum on low molecular weight permeate of ultra-filtered spent sulfite liquor (UF-SSL) from softwood pulping (stored at 4°C). For all experiments, C. glutamicum CR099::U pXMJ19 was used, which, in contrast to the wild-type, contains genes for improved mannose uptake and the ability to metabolize xylose integrated into the genome (denoted by ::U), as well as an empty plasmid for potential product biosynthetic genes. The valorization of UF-SSL was performed without additional prior detoxification steps such as bioling or overliming using a minimal medium based on UF-SSL.
The dataset consists of on-line data recorded during cultivation (pH, T, dO2, O2,offgas, CO2,offgas, weight of reactor and feeds, gassing, ...), off-line data of 9 samples per batch taken every 3h (BM; HPLC: glc, man, gal, ara, xyl, urea; Enzyme Assay: ace, lac, glu, NH4, PO4; ICP-MS: Na, Mg, Ca, Mn, Fe, Ni, Cu, Zn) and meta data (feed composition, quantity, density...). UF-SSL (42 g/L glucose, 135 g/L mannose, 57 g/L xylose, 29 g/L galactose, 13 g/L arabinose, 6.4 g/L acetate) was diluted with water to 25% (~10 g/L initial glucose concentration), sterile filtered (0.2µm) and supplemented (0.2 mg/L biotin, 12 mg/L chloramphenicol, 5 ml/L polyproylenglycol 2000). Trace elements were not added since sufficient amounts (relative to the defined medium) were present in the UF-SSL. Due to strong precipitation when PO4 was added to UF-SSL (containing 14 g/L Ca), a separate nitrogen and phosphate (NP) feed was used instead of mixing with the medium. The NP feed (66.4 g/L urea and 71.8 g/L KH2PO4, sterile filtered) was added at a constant feed rate ( V = 4.5 mL/h until 100 ml were fed) to the 1 L UF-SSL minimal medium batch volume in order to achive a CN ratio of ~1:10 and CP ratio of ~1:4 at full addition.</dc:description>
    <dc:subject>Bioprocess Optimization</dc:subject>
    <dc:subject>Bioprocess</dc:subject>
    <dc:subject>Fermentation</dc:subject>
    <dc:contributor id="https://orcid.org/0009-0001-5997-8789">Neudert, Mark-Richard</dc:contributor>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/n9jkwkrf4d.1</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/n9jkwkrf4d.1</dc:identifier>
    <dc:rights>Creative Commons Attribution 4.0 International</dc:rights>
    <dc:rights>http://creativecommons.org/licenses/by/4.0</dc:rights>
    <dc:relation>https://data.mendeley.com/datasets/n9jkwkrf4d</dc:relation>
    <dc:date>2024-05-28T08:29:38Z</dc:date>
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