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Identification of a polysaccharide produced by the pyruvate overproducer Candida glabrata CCTCC M202019
Candida glabrata has great potential for the accumulation of pyruvate as a preferred strain in pyruvate production by fermentation. However, its substrate conversion rate is relatively low. In this study, a novel polysaccharide containing α-1,4-glucosidic bonds was observed accidentally in screening...
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Published in: | Applied microbiology and biotechnology 2017-06, Vol.101 (11), p.4447-4458 |
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description | Candida glabrata
has great potential for the accumulation of pyruvate as a preferred strain in pyruvate production by fermentation. However, its substrate conversion rate is relatively low. In this study, a novel polysaccharide containing α-1,4-glucosidic bonds was observed accidentally in screening a high-titer pyruvate strain by atmospheric and room temperature plasma mutagenesis of
C. glabrata
. Chemical analysis of the partially purified polysaccharide S
4-C10
showed the main components were 1.2% (
w
/
w
) protein and 94.2% (
w
/
w
) total sugar. Fourier transform infrared and molecular mass distribution analysis indicated that the main component (PSG-2) of S
4-C10
was a small molecular homogeneous protein-bound polysaccharide. Monosaccharide analysis of PSG-2 showed it consisted of glucose, mannose, and fructose. By optimizing the vitamin mix content, 77.6 g L
−1
S
4-C10
polysaccharide could be obtained after 72 h fermentation at 30 °C in 500-mL flasks. RT-qPCR analysis showed that transcriptional level of some key genes related to polysaccharide biosynthesis was upregulated compared to that of wild-type strain. By knocking out two most significantly upregulated genes, CAGL0H02695g and CAGL0K10626g, in the wild-type strain, the pyruvate consumption rate was significantly reduced in late pyruvate fermentation phase, while the titer of polysaccharides was reduced by 18.0%. Besides the potential applications of the novel identified polysaccharide, this study provided clues for increasing the conversion ratio of glucose to pyruvate in
C. glabrata
by further decreasing the accumulation of polysaccharides. |
doi_str_mv | 10.1007/s00253-017-8245-1 |
format | article |
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has great potential for the accumulation of pyruvate as a preferred strain in pyruvate production by fermentation. However, its substrate conversion rate is relatively low. In this study, a novel polysaccharide containing α-1,4-glucosidic bonds was observed accidentally in screening a high-titer pyruvate strain by atmospheric and room temperature plasma mutagenesis of
C. glabrata
. Chemical analysis of the partially purified polysaccharide S
4-C10
showed the main components were 1.2% (
w
/
w
) protein and 94.2% (
w
/
w
) total sugar. Fourier transform infrared and molecular mass distribution analysis indicated that the main component (PSG-2) of S
4-C10
was a small molecular homogeneous protein-bound polysaccharide. Monosaccharide analysis of PSG-2 showed it consisted of glucose, mannose, and fructose. By optimizing the vitamin mix content, 77.6 g L
−1
S
4-C10
polysaccharide could be obtained after 72 h fermentation at 30 °C in 500-mL flasks. RT-qPCR analysis showed that transcriptional level of some key genes related to polysaccharide biosynthesis was upregulated compared to that of wild-type strain. By knocking out two most significantly upregulated genes, CAGL0H02695g and CAGL0K10626g, in the wild-type strain, the pyruvate consumption rate was significantly reduced in late pyruvate fermentation phase, while the titer of polysaccharides was reduced by 18.0%. Besides the potential applications of the novel identified polysaccharide, this study provided clues for increasing the conversion ratio of glucose to pyruvate in
C. glabrata
by further decreasing the accumulation of polysaccharides.</description><identifier>ISSN: 0175-7598</identifier><identifier>EISSN: 1432-0614</identifier><identifier>DOI: 10.1007/s00253-017-8245-1</identifier><identifier>PMID: 28343242</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Analysis ; Biomedical and Life Sciences ; Biosynthesis ; Biotechnological Products and Process Engineering ; Biotechnology ; Candida glabrata - drug effects ; Candida glabrata - genetics ; Candida glabrata - metabolism ; Chemical analysis ; Chemical bonds ; Conversion ; Conversion ratio ; Fermentation ; Flasks ; Fourier transforms ; Fructose ; Fungi ; Genes ; Glucose ; Glucose - metabolism ; Infrared analysis ; Life Sciences ; Mannose ; Mass distribution ; Microbial Genetics and Genomics ; Microbiology ; Monosaccharides - chemistry ; Mutagenesis ; Physiological aspects ; Polysaccharides ; Polysaccharides - biosynthesis ; Polysaccharides - chemistry ; Polysaccharides - isolation & purification ; Protein binding ; Proteins - metabolism ; Pyruvic acid ; Pyruvic Acid - metabolism ; Saccharides ; Sugar ; Temperature effects ; Transcription ; Transcription (Genetics) ; Vitamins - pharmacology</subject><ispartof>Applied microbiology and biotechnology, 2017-06, Vol.101 (11), p.4447-4458</ispartof><rights>Springer-Verlag Berlin Heidelberg 2017</rights><rights>COPYRIGHT 2017 Springer</rights><rights>Applied Microbiology and Biotechnology is a copyright of Springer, 2017.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c510t-819668492008e5eeceaf77e80f27d062052e8709beb3ea9655a7d14f3cdac03d3</citedby><cites>FETCH-LOGICAL-c510t-819668492008e5eeceaf77e80f27d062052e8709beb3ea9655a7d14f3cdac03d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1901421340/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1901421340?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,780,784,11686,27922,27923,36058,44361,74665</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28343242$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Luo, Zhengshan</creatorcontrib><creatorcontrib>Liu, Song</creatorcontrib><creatorcontrib>Du, Guocheng</creatorcontrib><creatorcontrib>Zhou, Jingwen</creatorcontrib><creatorcontrib>Chen, Jian</creatorcontrib><title>Identification of a polysaccharide produced by the pyruvate overproducer Candida glabrata CCTCC M202019</title><title>Applied microbiology and biotechnology</title><addtitle>Appl Microbiol Biotechnol</addtitle><addtitle>Appl Microbiol Biotechnol</addtitle><description>Candida glabrata
has great potential for the accumulation of pyruvate as a preferred strain in pyruvate production by fermentation. However, its substrate conversion rate is relatively low. In this study, a novel polysaccharide containing α-1,4-glucosidic bonds was observed accidentally in screening a high-titer pyruvate strain by atmospheric and room temperature plasma mutagenesis of
C. glabrata
. Chemical analysis of the partially purified polysaccharide S
4-C10
showed the main components were 1.2% (
w
/
w
) protein and 94.2% (
w
/
w
) total sugar. Fourier transform infrared and molecular mass distribution analysis indicated that the main component (PSG-2) of S
4-C10
was a small molecular homogeneous protein-bound polysaccharide. Monosaccharide analysis of PSG-2 showed it consisted of glucose, mannose, and fructose. By optimizing the vitamin mix content, 77.6 g L
−1
S
4-C10
polysaccharide could be obtained after 72 h fermentation at 30 °C in 500-mL flasks. RT-qPCR analysis showed that transcriptional level of some key genes related to polysaccharide biosynthesis was upregulated compared to that of wild-type strain. By knocking out two most significantly upregulated genes, CAGL0H02695g and CAGL0K10626g, in the wild-type strain, the pyruvate consumption rate was significantly reduced in late pyruvate fermentation phase, while the titer of polysaccharides was reduced by 18.0%. Besides the potential applications of the novel identified polysaccharide, this study provided clues for increasing the conversion ratio of glucose to pyruvate in
C. glabrata
by further decreasing the accumulation of polysaccharides.</description><subject>Analysis</subject><subject>Biomedical and Life Sciences</subject><subject>Biosynthesis</subject><subject>Biotechnological Products and Process Engineering</subject><subject>Biotechnology</subject><subject>Candida glabrata - drug effects</subject><subject>Candida glabrata - genetics</subject><subject>Candida glabrata - metabolism</subject><subject>Chemical analysis</subject><subject>Chemical bonds</subject><subject>Conversion</subject><subject>Conversion ratio</subject><subject>Fermentation</subject><subject>Flasks</subject><subject>Fourier transforms</subject><subject>Fructose</subject><subject>Fungi</subject><subject>Genes</subject><subject>Glucose</subject><subject>Glucose - metabolism</subject><subject>Infrared analysis</subject><subject>Life Sciences</subject><subject>Mannose</subject><subject>Mass distribution</subject><subject>Microbial Genetics and Genomics</subject><subject>Microbiology</subject><subject>Monosaccharides - chemistry</subject><subject>Mutagenesis</subject><subject>Physiological aspects</subject><subject>Polysaccharides</subject><subject>Polysaccharides - biosynthesis</subject><subject>Polysaccharides - chemistry</subject><subject>Polysaccharides - isolation & purification</subject><subject>Protein binding</subject><subject>Proteins - metabolism</subject><subject>Pyruvic acid</subject><subject>Pyruvic Acid - metabolism</subject><subject>Saccharides</subject><subject>Sugar</subject><subject>Temperature effects</subject><subject>Transcription</subject><subject>Transcription (Genetics)</subject><subject>Vitamins - pharmacology</subject><issn>0175-7598</issn><issn>1432-0614</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>M0C</sourceid><recordid>eNp1kUtv1DAUhS0EokPhB7BBllixSLl24sRZVhGUkYqQoKytG_smdTWTDLZTMf--rmZ4jATywrLPd-5Dh7HXAi4EQPM-AkhVFiCaQstKFeIJW4mqlAXUonrKVllQRaNafcZexHgHIKSu6-fsTOoyY5VcsXHtaEp-8BaTnyc-Dxz5bt7sI1p7i8E74rswu8WS4_2ep9v83oflHhPx-Z7CUQy8w8l5h3zcYB8wIe-6m67jnyVIEO1L9mzATaRXx_ucff_44ab7VFx_uVp3l9eFVQJSoUVb17pqJYAmRWQJh6YhDYNsHNQSlCTdQNtTXxK2tVLYOFENpXVooXTlOXt7qJvn-rFQTOZuXsKUWxrRgqikKCv4Q424IeOnYU4B7dZHay5VHqSUrdaZuvgHlY-jrbfzRIPP_yeGdyeGzCT6mUZcYjTrb19PWXFgbZhjDDSYXfBbDHsjwDymaw7pmhyieUzXiOx5c1xu6bfkfjt-xZkBeQBilqaRwl_b_7fqA65Vq8I</recordid><startdate>20170601</startdate><enddate>20170601</enddate><creator>Luo, Zhengshan</creator><creator>Liu, Song</creator><creator>Du, Guocheng</creator><creator>Zhou, Jingwen</creator><creator>Chen, Jian</creator><general>Springer Berlin Heidelberg</general><general>Springer</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>3V.</scope><scope>7QL</scope><scope>7T7</scope><scope>7WY</scope><scope>7WZ</scope><scope>7X7</scope><scope>7XB</scope><scope>87Z</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8FL</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BEZIV</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FRNLG</scope><scope>FYUFA</scope><scope>F~G</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K60</scope><scope>K6~</scope><scope>K9.</scope><scope>L.-</scope><scope>LK8</scope><scope>M0C</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQBIZ</scope><scope>PQBZA</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope></search><sort><creationdate>20170601</creationdate><title>Identification of a polysaccharide produced by the pyruvate overproducer Candida glabrata CCTCC M202019</title><author>Luo, Zhengshan ; Liu, Song ; Du, Guocheng ; Zhou, Jingwen ; Chen, Jian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c510t-819668492008e5eeceaf77e80f27d062052e8709beb3ea9655a7d14f3cdac03d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Analysis</topic><topic>Biomedical and Life Sciences</topic><topic>Biosynthesis</topic><topic>Biotechnological Products and Process Engineering</topic><topic>Biotechnology</topic><topic>Candida glabrata - 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has great potential for the accumulation of pyruvate as a preferred strain in pyruvate production by fermentation. However, its substrate conversion rate is relatively low. In this study, a novel polysaccharide containing α-1,4-glucosidic bonds was observed accidentally in screening a high-titer pyruvate strain by atmospheric and room temperature plasma mutagenesis of
C. glabrata
. Chemical analysis of the partially purified polysaccharide S
4-C10
showed the main components were 1.2% (
w
/
w
) protein and 94.2% (
w
/
w
) total sugar. Fourier transform infrared and molecular mass distribution analysis indicated that the main component (PSG-2) of S
4-C10
was a small molecular homogeneous protein-bound polysaccharide. Monosaccharide analysis of PSG-2 showed it consisted of glucose, mannose, and fructose. By optimizing the vitamin mix content, 77.6 g L
−1
S
4-C10
polysaccharide could be obtained after 72 h fermentation at 30 °C in 500-mL flasks. RT-qPCR analysis showed that transcriptional level of some key genes related to polysaccharide biosynthesis was upregulated compared to that of wild-type strain. By knocking out two most significantly upregulated genes, CAGL0H02695g and CAGL0K10626g, in the wild-type strain, the pyruvate consumption rate was significantly reduced in late pyruvate fermentation phase, while the titer of polysaccharides was reduced by 18.0%. Besides the potential applications of the novel identified polysaccharide, this study provided clues for increasing the conversion ratio of glucose to pyruvate in
C. glabrata
by further decreasing the accumulation of polysaccharides.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>28343242</pmid><doi>10.1007/s00253-017-8245-1</doi><tpages>12</tpages></addata></record> |
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subjects | Analysis Biomedical and Life Sciences Biosynthesis Biotechnological Products and Process Engineering Biotechnology Candida glabrata - drug effects Candida glabrata - genetics Candida glabrata - metabolism Chemical analysis Chemical bonds Conversion Conversion ratio Fermentation Flasks Fourier transforms Fructose Fungi Genes Glucose Glucose - metabolism Infrared analysis Life Sciences Mannose Mass distribution Microbial Genetics and Genomics Microbiology Monosaccharides - chemistry Mutagenesis Physiological aspects Polysaccharides Polysaccharides - biosynthesis Polysaccharides - chemistry Polysaccharides - isolation & purification Protein binding Proteins - metabolism Pyruvic acid Pyruvic Acid - metabolism Saccharides Sugar Temperature effects Transcription Transcription (Genetics) Vitamins - pharmacology |
title | Identification of a polysaccharide produced by the pyruvate overproducer Candida glabrata CCTCC M202019 |
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