Morphology engineering of Aspergillus niger for improved enzyme production
Supplementation with silicate microparticles was used as novel approach to control the morphological development of Aspergillus niger, important as the major world source of citric acid and higher-value enzymes, in submerged culture. With careful variation of size and concentration of the micromater...
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description | Supplementation with silicate microparticles was used as novel approach to control the morphological development of Aspergillus niger, important as the major world source of citric acid and higher-value enzymes, in submerged culture. With careful variation of size and concentration of the micromaterial added, a number of distinct morphological forms including pellets of different size, free dispersed mycelium, and short hyphae fragments could be reproducibly created. Aluminum oxide particles similarly affected morphology, showing that this effect is largely independent of the chemical particle composition. Image analysis of morphological development of A. niger during the cultivation process showed that the microparticles influence the morphology by collision-induced disruption of conidia aggregates and probably also the hindrance of new spore-spore interactions in the very early stage of the process. Exemplified for different recombinant A. niger strains enzyme production could be strongly enhanced by the addition of microparticles. Linked to the formation of freely dispersed mycelium, titers for glucoamylase (GA) expressed as intracellular enzyme (88 U/mL) and fructofuranosidase secreted into the supernatant (77 U/mL), were up to fourfold higher in shake flasks. Moreover, accumulation of the undesired by-product oxalate was suppressed by up to 90%. The microparticle strategy could be successfully transferred to fructofuranosidase production in bioreactor, where a final titer of 160 U/mL could be reached. Using co-expression of GA with green fluorescent protein, enzyme production was localized in the cellular aggregates of A. niger. For pelleted growth, protein production was maximal only within a thin layer at the pellet surface and markedly decreased in the pellet interior, whereas the interaction with the microparticles created a highly active biocatalyst with the dominant fraction of cells contributing to production. Biotechnol. Bioeng. 2010;105: 1058-1068. |
doi_str_mv | 10.1002/bit.22614 |
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With careful variation of size and concentration of the micromaterial added, a number of distinct morphological forms including pellets of different size, free dispersed mycelium, and short hyphae fragments could be reproducibly created. Aluminum oxide particles similarly affected morphology, showing that this effect is largely independent of the chemical particle composition. Image analysis of morphological development of A. niger during the cultivation process showed that the microparticles influence the morphology by collision-induced disruption of conidia aggregates and probably also the hindrance of new spore-spore interactions in the very early stage of the process. Exemplified for different recombinant A. niger strains enzyme production could be strongly enhanced by the addition of microparticles. Linked to the formation of freely dispersed mycelium, titers for glucoamylase (GA) expressed as intracellular enzyme (88 U/mL) and fructofuranosidase secreted into the supernatant (77 U/mL), were up to fourfold higher in shake flasks. Moreover, accumulation of the undesired by-product oxalate was suppressed by up to 90%. The microparticle strategy could be successfully transferred to fructofuranosidase production in bioreactor, where a final titer of 160 U/mL could be reached. Using co-expression of GA with green fluorescent protein, enzyme production was localized in the cellular aggregates of A. niger. For pelleted growth, protein production was maximal only within a thin layer at the pellet surface and markedly decreased in the pellet interior, whereas the interaction with the microparticles created a highly active biocatalyst with the dominant fraction of cells contributing to production. Biotechnol. Bioeng. 2010;105: 1058-1068.</description><identifier>ISSN: 0006-3592</identifier><identifier>EISSN: 1097-0290</identifier><identifier>DOI: 10.1002/bit.22614</identifier><identifier>PMID: 19953678</identifier><identifier>CODEN: BIBIAU</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Aluminum Oxide - chemistry ; Aspergillus niger - cytology ; Aspergillus niger - enzymology ; Aspergillus niger - genetics ; beta-Fructofuranosidase - biosynthesis ; beta-Fructofuranosidase - genetics ; Bioengineering ; Biological and medical sciences ; Biotechnology ; Cell culture ; Cell Culture Techniques - methods ; Chemical compounds ; Enzymes ; filamentous fungi ; Fundamental and applied biological sciences. 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Bioeng</addtitle><description>Supplementation with silicate microparticles was used as novel approach to control the morphological development of Aspergillus niger, important as the major world source of citric acid and higher-value enzymes, in submerged culture. With careful variation of size and concentration of the micromaterial added, a number of distinct morphological forms including pellets of different size, free dispersed mycelium, and short hyphae fragments could be reproducibly created. Aluminum oxide particles similarly affected morphology, showing that this effect is largely independent of the chemical particle composition. Image analysis of morphological development of A. niger during the cultivation process showed that the microparticles influence the morphology by collision-induced disruption of conidia aggregates and probably also the hindrance of new spore-spore interactions in the very early stage of the process. Exemplified for different recombinant A. niger strains enzyme production could be strongly enhanced by the addition of microparticles. Linked to the formation of freely dispersed mycelium, titers for glucoamylase (GA) expressed as intracellular enzyme (88 U/mL) and fructofuranosidase secreted into the supernatant (77 U/mL), were up to fourfold higher in shake flasks. Moreover, accumulation of the undesired by-product oxalate was suppressed by up to 90%. The microparticle strategy could be successfully transferred to fructofuranosidase production in bioreactor, where a final titer of 160 U/mL could be reached. Using co-expression of GA with green fluorescent protein, enzyme production was localized in the cellular aggregates of A. niger. For pelleted growth, protein production was maximal only within a thin layer at the pellet surface and markedly decreased in the pellet interior, whereas the interaction with the microparticles created a highly active biocatalyst with the dominant fraction of cells contributing to production. Biotechnol. Bioeng. 2010;105: 1058-1068.</description><subject>Aluminum Oxide - chemistry</subject><subject>Aspergillus niger - cytology</subject><subject>Aspergillus niger - enzymology</subject><subject>Aspergillus niger - genetics</subject><subject>beta-Fructofuranosidase - biosynthesis</subject><subject>beta-Fructofuranosidase - genetics</subject><subject>Bioengineering</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Cell culture</subject><subject>Cell Culture Techniques - methods</subject><subject>Chemical compounds</subject><subject>Enzymes</subject><subject>filamentous fungi</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fungi</subject><subject>Gene expression</subject><subject>Glucan 1,4-alpha-Glucosidase - biosynthesis</subject><subject>Glucan 1,4-alpha-Glucosidase - genetics</subject><subject>Glucose - metabolism</subject><subject>Green Fluorescent Proteins - biosynthesis</subject><subject>Green Fluorescent Proteins - genetics</subject><subject>Hydrogen-Ion Concentration</subject><subject>Hyphae - cytology</subject><subject>Hyphae - metabolism</subject><subject>Kinetics</subject><subject>microparticle</subject><subject>Microspheres</subject><subject>Morphology</subject><subject>mycelium</subject><subject>Mycelium - cytology</subject><subject>Mycelium - enzymology</subject><subject>Mycology - methods</subject><subject>Particle Size</subject><subject>pellet</subject><subject>Protein Engineering - methods</subject><subject>Recombinant Proteins - biosynthesis</subject><subject>Recombinant Proteins - genetics</subject><subject>submerged cultivation</subject><issn>0006-3592</issn><issn>1097-0290</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10E1v1DAQBmALUdGlcOAPQISEUA9pPXbsxMdSQVso3616tJxkHNwm8WJvoNtfj0uWIiFxGo30zIdeQp4A3QNK2X7tVnuMSSjukQVQVeaUKXqfLCilMudCsW3yMMbL1JaVlA_INigluCyrBXn73oflN9_7bp3h2LkRMbixy7zNDuISQ-f6forZ6DoMmfUhc8My-B_YJn2zHjBLXTs1K-fHR2TLmj7i403dIedvXp8dHuenH49ODg9O80ZQVeSScrR1mx6wXFTIbIGW1TWnNTUWVIPSWgAuGMcGWyaVQlGVFatogaIVwHfIy3lvOv19wrjSg4sN9r0Z0U9Rl5xLJUDeyuf_yEs_hTE9pxnwUtKUXkK7M2qCjzGg1cvgBhPWGqi-jVenePXveJN9ulk41QO2f-UmzwRebICJjeltMGPj4p1jTBSi5GVy-7P76Xpc__-ifnVy9ud0Pk-4uMLruwkTrrRMG4W--HCkP737zOHiy7FWyT-bvTVemy6kL86_MgqcQgVQguK_AMlSqPQ</recordid><startdate>20100415</startdate><enddate>20100415</enddate><creator>Driouch, Habib</creator><creator>Sommer, Becky</creator><creator>Wittmann, Christoph</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><general>Wiley Subscription Services, Inc</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><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>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7T7</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20100415</creationdate><title>Morphology engineering of Aspergillus niger for improved enzyme production</title><author>Driouch, Habib ; Sommer, Becky ; Wittmann, Christoph</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5094-603efbd953f358e2f4ef2bb30b0af19ce6ff113523eced2699e58782804e5d513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Aluminum Oxide - chemistry</topic><topic>Aspergillus niger - cytology</topic><topic>Aspergillus niger - enzymology</topic><topic>Aspergillus niger - genetics</topic><topic>beta-Fructofuranosidase - biosynthesis</topic><topic>beta-Fructofuranosidase - genetics</topic><topic>Bioengineering</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Cell culture</topic><topic>Cell Culture Techniques - methods</topic><topic>Chemical compounds</topic><topic>Enzymes</topic><topic>filamentous fungi</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fungi</topic><topic>Gene expression</topic><topic>Glucan 1,4-alpha-Glucosidase - biosynthesis</topic><topic>Glucan 1,4-alpha-Glucosidase - genetics</topic><topic>Glucose - metabolism</topic><topic>Green Fluorescent Proteins - biosynthesis</topic><topic>Green Fluorescent Proteins - genetics</topic><topic>Hydrogen-Ion Concentration</topic><topic>Hyphae - cytology</topic><topic>Hyphae - metabolism</topic><topic>Kinetics</topic><topic>microparticle</topic><topic>Microspheres</topic><topic>Morphology</topic><topic>mycelium</topic><topic>Mycelium - cytology</topic><topic>Mycelium - enzymology</topic><topic>Mycology - methods</topic><topic>Particle Size</topic><topic>pellet</topic><topic>Protein Engineering - methods</topic><topic>Recombinant Proteins - biosynthesis</topic><topic>Recombinant Proteins - genetics</topic><topic>submerged cultivation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Driouch, Habib</creatorcontrib><creatorcontrib>Sommer, Becky</creatorcontrib><creatorcontrib>Wittmann, Christoph</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biotechnology and bioengineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Driouch, Habib</au><au>Sommer, Becky</au><au>Wittmann, Christoph</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Morphology engineering of Aspergillus niger for improved enzyme production</atitle><jtitle>Biotechnology and bioengineering</jtitle><addtitle>Biotechnol. Bioeng</addtitle><date>2010-04-15</date><risdate>2010</risdate><volume>105</volume><issue>6</issue><spage>1058</spage><epage>1068</epage><pages>1058-1068</pages><issn>0006-3592</issn><eissn>1097-0290</eissn><coden>BIBIAU</coden><abstract>Supplementation with silicate microparticles was used as novel approach to control the morphological development of Aspergillus niger, important as the major world source of citric acid and higher-value enzymes, in submerged culture. With careful variation of size and concentration of the micromaterial added, a number of distinct morphological forms including pellets of different size, free dispersed mycelium, and short hyphae fragments could be reproducibly created. Aluminum oxide particles similarly affected morphology, showing that this effect is largely independent of the chemical particle composition. Image analysis of morphological development of A. niger during the cultivation process showed that the microparticles influence the morphology by collision-induced disruption of conidia aggregates and probably also the hindrance of new spore-spore interactions in the very early stage of the process. Exemplified for different recombinant A. niger strains enzyme production could be strongly enhanced by the addition of microparticles. Linked to the formation of freely dispersed mycelium, titers for glucoamylase (GA) expressed as intracellular enzyme (88 U/mL) and fructofuranosidase secreted into the supernatant (77 U/mL), were up to fourfold higher in shake flasks. Moreover, accumulation of the undesired by-product oxalate was suppressed by up to 90%. The microparticle strategy could be successfully transferred to fructofuranosidase production in bioreactor, where a final titer of 160 U/mL could be reached. Using co-expression of GA with green fluorescent protein, enzyme production was localized in the cellular aggregates of A. niger. For pelleted growth, protein production was maximal only within a thin layer at the pellet surface and markedly decreased in the pellet interior, whereas the interaction with the microparticles created a highly active biocatalyst with the dominant fraction of cells contributing to production. Biotechnol. Bioeng. 2010;105: 1058-1068.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>19953678</pmid><doi>10.1002/bit.22614</doi><tpages>11</tpages></addata></record> |
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subjects | Aluminum Oxide - chemistry Aspergillus niger - cytology Aspergillus niger - enzymology Aspergillus niger - genetics beta-Fructofuranosidase - biosynthesis beta-Fructofuranosidase - genetics Bioengineering Biological and medical sciences Biotechnology Cell culture Cell Culture Techniques - methods Chemical compounds Enzymes filamentous fungi Fundamental and applied biological sciences. Psychology Fungi Gene expression Glucan 1,4-alpha-Glucosidase - biosynthesis Glucan 1,4-alpha-Glucosidase - genetics Glucose - metabolism Green Fluorescent Proteins - biosynthesis Green Fluorescent Proteins - genetics Hydrogen-Ion Concentration Hyphae - cytology Hyphae - metabolism Kinetics microparticle Microspheres Morphology mycelium Mycelium - cytology Mycelium - enzymology Mycology - methods Particle Size pellet Protein Engineering - methods Recombinant Proteins - biosynthesis Recombinant Proteins - genetics submerged cultivation |
title | Morphology engineering of Aspergillus niger for improved enzyme production |
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