Sodium starch octenyl succinate facilitated the production of water-soluble yellow pigments in Monascus ruber fermentation
Natural water-soluble Monascus pigments (WSMPs) have been in increasing demand but have not been able to achieve industrial production due to the low production rate. This study aimed to improve the biosynthesis and secretion of extracellular yellow pigments (EYPs) through submerged fermentation wit...
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creator | Huang, Zhen-feng Yang, Shan-zhong Liu, Hai-qing Tian, Xiao-fei Wu, Zhen-qiang |
description | Natural water-soluble
Monascus
pigments (WSMPs) have been in increasing demand but have not been able to achieve industrial production due to the low production rate. This study aimed to improve the biosynthesis and secretion of extracellular yellow pigments (EYPs) through submerged fermentation with
Monascus ruber
CGMCC 10,910 supplemented with sodium starch octenyl succinate (OSA-SNa). The results demonstrated that the yield was 69.68% and 48.89% higher than that without OSA-SNa in conventional fermentation (CF) and extractive fermentation (EF), respectively. The mainly increased EYP components were Y3 and Y4 in CF, but they were mainly Y1 and Y2 as well as secreted intracellular pigments, including Y5, Y6, O1, and O2, in EF. Scanning electron microscopy analysis revealed that the mycelium presented an uneven surface profile with obvious wrinkles and small fragments with OSA-SNa. It was found that a higher unsaturated/saturated fatty acids ratio in the cell membrane resulted in increased permeability and facilitated the export of intracellular yellow pigments into the broth with OSA-SNa treatment. In addition, a higher NAD
+
/NADH ratio and glucose-6-phosphate dehydrogenase activity provided a reducing condition for yellow pigment biosynthesis. Gene expression analysis showed that the expression levels of the key genes for yellow pigment biosynthesis were significantly upregulated by OSA-SNa. This study provides an effective strategy to promote the production of WSMPs by microparticle-enhanced cultivation using OSA-SNa.
Key points
•
OSA-SNa addition facilitated the production of Monascus yellow pigments.
•
Mycelial morphology and membrane permeability were affected by OSA-SNa.
•
The key gene expression of yellow pigments was upregulated.
Graphical abstract |
doi_str_mv | 10.1007/s00253-021-11512-7 |
format | Article |
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Monascus
pigments (WSMPs) have been in increasing demand but have not been able to achieve industrial production due to the low production rate. This study aimed to improve the biosynthesis and secretion of extracellular yellow pigments (EYPs) through submerged fermentation with
Monascus ruber
CGMCC 10,910 supplemented with sodium starch octenyl succinate (OSA-SNa). The results demonstrated that the yield was 69.68% and 48.89% higher than that without OSA-SNa in conventional fermentation (CF) and extractive fermentation (EF), respectively. The mainly increased EYP components were Y3 and Y4 in CF, but they were mainly Y1 and Y2 as well as secreted intracellular pigments, including Y5, Y6, O1, and O2, in EF. Scanning electron microscopy analysis revealed that the mycelium presented an uneven surface profile with obvious wrinkles and small fragments with OSA-SNa. It was found that a higher unsaturated/saturated fatty acids ratio in the cell membrane resulted in increased permeability and facilitated the export of intracellular yellow pigments into the broth with OSA-SNa treatment. In addition, a higher NAD
+
/NADH ratio and glucose-6-phosphate dehydrogenase activity provided a reducing condition for yellow pigment biosynthesis. Gene expression analysis showed that the expression levels of the key genes for yellow pigment biosynthesis were significantly upregulated by OSA-SNa. This study provides an effective strategy to promote the production of WSMPs by microparticle-enhanced cultivation using OSA-SNa.
Key points
•
OSA-SNa addition facilitated the production of Monascus yellow pigments.
•
Mycelial morphology and membrane permeability were affected by OSA-SNa.
•
The key gene expression of yellow pigments was upregulated.
Graphical abstract</description><identifier>ISSN: 0175-7598</identifier><identifier>EISSN: 1432-0614</identifier><identifier>DOI: 10.1007/s00253-021-11512-7</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Analysis ; Biomedical and Life Sciences ; Biosynthesis ; Biotechnological Products and Process Engineering ; Biotechnology ; Cell membranes ; Fatty acids ; Fermentation ; Gene expression ; Genetic aspects ; Glucose 6 phosphate dehydrogenase ; Glucosephosphate dehydrogenase ; Identification and classification ; Industrial production ; Intracellular ; Life Sciences ; Membrane permeability ; Methods ; Microbial Genetics and Genomics ; Microbiology ; Microparticles ; Monascus ; Monascus ruber ; Morphology ; Mycelia ; NAD ; NADH ; Nicotinamide adenine dinucleotide ; Organic pigments ; Permeability ; Pigments ; Scanning electron microscopy ; Sodium ; Starch ; Water chemistry</subject><ispartof>Applied microbiology and biotechnology, 2021-09, Vol.105 (18), p.6691-6706</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021</rights><rights>COPYRIGHT 2021 Springer</rights><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c453t-f1735dc65366c720a6060889f959722daa17763b6c8cf57a0a7f5033d1aab62e3</citedby><cites>FETCH-LOGICAL-c453t-f1735dc65366c720a6060889f959722daa17763b6c8cf57a0a7f5033d1aab62e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00253-021-11512-7$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00253-021-11512-7$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,777,781,27905,27906,41469,42538,51300</link.rule.ids></links><search><creatorcontrib>Huang, Zhen-feng</creatorcontrib><creatorcontrib>Yang, Shan-zhong</creatorcontrib><creatorcontrib>Liu, Hai-qing</creatorcontrib><creatorcontrib>Tian, Xiao-fei</creatorcontrib><creatorcontrib>Wu, Zhen-qiang</creatorcontrib><title>Sodium starch octenyl succinate facilitated the production of water-soluble yellow pigments in Monascus ruber fermentation</title><title>Applied microbiology and biotechnology</title><addtitle>Appl Microbiol Biotechnol</addtitle><description>Natural water-soluble
Monascus
pigments (WSMPs) have been in increasing demand but have not been able to achieve industrial production due to the low production rate. This study aimed to improve the biosynthesis and secretion of extracellular yellow pigments (EYPs) through submerged fermentation with
Monascus ruber
CGMCC 10,910 supplemented with sodium starch octenyl succinate (OSA-SNa). The results demonstrated that the yield was 69.68% and 48.89% higher than that without OSA-SNa in conventional fermentation (CF) and extractive fermentation (EF), respectively. The mainly increased EYP components were Y3 and Y4 in CF, but they were mainly Y1 and Y2 as well as secreted intracellular pigments, including Y5, Y6, O1, and O2, in EF. Scanning electron microscopy analysis revealed that the mycelium presented an uneven surface profile with obvious wrinkles and small fragments with OSA-SNa. It was found that a higher unsaturated/saturated fatty acids ratio in the cell membrane resulted in increased permeability and facilitated the export of intracellular yellow pigments into the broth with OSA-SNa treatment. In addition, a higher NAD
+
/NADH ratio and glucose-6-phosphate dehydrogenase activity provided a reducing condition for yellow pigment biosynthesis. Gene expression analysis showed that the expression levels of the key genes for yellow pigment biosynthesis were significantly upregulated by OSA-SNa. This study provides an effective strategy to promote the production of WSMPs by microparticle-enhanced cultivation using OSA-SNa.
Key points
•
OSA-SNa addition facilitated the production of Monascus yellow pigments.
•
Mycelial morphology and membrane permeability were affected by OSA-SNa.
•
The key gene expression of yellow pigments was upregulated.
Graphical abstract</description><subject>Analysis</subject><subject>Biomedical and Life Sciences</subject><subject>Biosynthesis</subject><subject>Biotechnological Products and Process Engineering</subject><subject>Biotechnology</subject><subject>Cell membranes</subject><subject>Fatty acids</subject><subject>Fermentation</subject><subject>Gene expression</subject><subject>Genetic aspects</subject><subject>Glucose 6 phosphate dehydrogenase</subject><subject>Glucosephosphate dehydrogenase</subject><subject>Identification and classification</subject><subject>Industrial production</subject><subject>Intracellular</subject><subject>Life Sciences</subject><subject>Membrane permeability</subject><subject>Methods</subject><subject>Microbial Genetics and Genomics</subject><subject>Microbiology</subject><subject>Microparticles</subject><subject>Monascus</subject><subject>Monascus ruber</subject><subject>Morphology</subject><subject>Mycelia</subject><subject>NAD</subject><subject>NADH</subject><subject>Nicotinamide adenine dinucleotide</subject><subject>Organic pigments</subject><subject>Permeability</subject><subject>Pigments</subject><subject>Scanning electron microscopy</subject><subject>Sodium</subject><subject>Starch</subject><subject>Water chemistry</subject><issn>0175-7598</issn><issn>1432-0614</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kkuLFDEUhQtRsB39A64CbnSRMY9KUrUcBh8DI4Kj63A7lfRkqEraPBjbX2_KFoYWkSwSbr5zOBdO172k5JwSot5mQpjgmDCKKRWUYfWo29CeM0wk7R93G0KVwEqMw9PuWc53hFA2SLnpft7EydcF5QLJ3KJoig2HGeVqjA9QLHJg_OxLe06o3Fq0T3GqpvgYUHTovs0TznGu29mig53neI_2frfYUDLyAX2KAbKpGaW6tQk5m9YvWPXPuycO5mxf_LnPum_v3329_IivP3-4ury4xqYXvGBHFReTkYJLaRQjIIkkwzC6UYyKsQmAKiX5VprBOKGAgHKCcD5RgK1klp91r4--Lfr3anPRi8-mRYVgY82aCanGgY5cNPTVX-hdrCm0dI1SzZSMw_hA7WC22gcXSwKzmuoLqfqBqb5fqfN_UO1MdvEmBut8m58I3pwIGlPsj7KDmrO-uvlyyrIja1LMOVmn98kvkA6aEr02Qh8boVsj9O9GaNVE_CjKDQ47mx62-4_qFyOQuCQ</recordid><startdate>20210901</startdate><enddate>20210901</enddate><creator>Huang, 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starch octenyl succinate facilitated the production of water-soluble yellow pigments in Monascus ruber fermentation</title><author>Huang, Zhen-feng ; Yang, Shan-zhong ; Liu, Hai-qing ; Tian, Xiao-fei ; Wu, Zhen-qiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c453t-f1735dc65366c720a6060889f959722daa17763b6c8cf57a0a7f5033d1aab62e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Analysis</topic><topic>Biomedical and Life Sciences</topic><topic>Biosynthesis</topic><topic>Biotechnological Products and Process Engineering</topic><topic>Biotechnology</topic><topic>Cell membranes</topic><topic>Fatty acids</topic><topic>Fermentation</topic><topic>Gene expression</topic><topic>Genetic aspects</topic><topic>Glucose 6 phosphate dehydrogenase</topic><topic>Glucosephosphate dehydrogenase</topic><topic>Identification and classification</topic><topic>Industrial production</topic><topic>Intracellular</topic><topic>Life Sciences</topic><topic>Membrane permeability</topic><topic>Methods</topic><topic>Microbial Genetics and Genomics</topic><topic>Microbiology</topic><topic>Microparticles</topic><topic>Monascus</topic><topic>Monascus ruber</topic><topic>Morphology</topic><topic>Mycelia</topic><topic>NAD</topic><topic>NADH</topic><topic>Nicotinamide adenine dinucleotide</topic><topic>Organic pigments</topic><topic>Permeability</topic><topic>Pigments</topic><topic>Scanning electron microscopy</topic><topic>Sodium</topic><topic>Starch</topic><topic>Water chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, Zhen-feng</creatorcontrib><creatorcontrib>Yang, Shan-zhong</creatorcontrib><creatorcontrib>Liu, Hai-qing</creatorcontrib><creatorcontrib>Tian, Xiao-fei</creatorcontrib><creatorcontrib>Wu, Zhen-qiang</creatorcontrib><collection>CrossRef</collection><collection>Gale In Context: 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Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Applied microbiology and biotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, Zhen-feng</au><au>Yang, Shan-zhong</au><au>Liu, Hai-qing</au><au>Tian, Xiao-fei</au><au>Wu, Zhen-qiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sodium starch octenyl succinate facilitated the production of water-soluble yellow pigments in Monascus ruber fermentation</atitle><jtitle>Applied microbiology and biotechnology</jtitle><stitle>Appl Microbiol Biotechnol</stitle><date>2021-09-01</date><risdate>2021</risdate><volume>105</volume><issue>18</issue><spage>6691</spage><epage>6706</epage><pages>6691-6706</pages><issn>0175-7598</issn><eissn>1432-0614</eissn><abstract>Natural water-soluble
Monascus
pigments (WSMPs) have been in increasing demand but have not been able to achieve industrial production due to the low production rate. This study aimed to improve the biosynthesis and secretion of extracellular yellow pigments (EYPs) through submerged fermentation with
Monascus ruber
CGMCC 10,910 supplemented with sodium starch octenyl succinate (OSA-SNa). The results demonstrated that the yield was 69.68% and 48.89% higher than that without OSA-SNa in conventional fermentation (CF) and extractive fermentation (EF), respectively. The mainly increased EYP components were Y3 and Y4 in CF, but they were mainly Y1 and Y2 as well as secreted intracellular pigments, including Y5, Y6, O1, and O2, in EF. Scanning electron microscopy analysis revealed that the mycelium presented an uneven surface profile with obvious wrinkles and small fragments with OSA-SNa. It was found that a higher unsaturated/saturated fatty acids ratio in the cell membrane resulted in increased permeability and facilitated the export of intracellular yellow pigments into the broth with OSA-SNa treatment. In addition, a higher NAD
+
/NADH ratio and glucose-6-phosphate dehydrogenase activity provided a reducing condition for yellow pigment biosynthesis. Gene expression analysis showed that the expression levels of the key genes for yellow pigment biosynthesis were significantly upregulated by OSA-SNa. This study provides an effective strategy to promote the production of WSMPs by microparticle-enhanced cultivation using OSA-SNa.
Key points
•
OSA-SNa addition facilitated the production of Monascus yellow pigments.
•
Mycelial morphology and membrane permeability were affected by OSA-SNa.
•
The key gene expression of yellow pigments was upregulated.
Graphical abstract</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><doi>10.1007/s00253-021-11512-7</doi><tpages>16</tpages></addata></record> |
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subjects | Analysis Biomedical and Life Sciences Biosynthesis Biotechnological Products and Process Engineering Biotechnology Cell membranes Fatty acids Fermentation Gene expression Genetic aspects Glucose 6 phosphate dehydrogenase Glucosephosphate dehydrogenase Identification and classification Industrial production Intracellular Life Sciences Membrane permeability Methods Microbial Genetics and Genomics Microbiology Microparticles Monascus Monascus ruber Morphology Mycelia NAD NADH Nicotinamide adenine dinucleotide Organic pigments Permeability Pigments Scanning electron microscopy Sodium Starch Water chemistry |
title | Sodium starch octenyl succinate facilitated the production of water-soluble yellow pigments in Monascus ruber fermentation |
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