Exploring Thermophilic Cellulolytic Enzyme Production Potential of Aspergillus fumigatus by the Solid-State Fermentation of Wheat Straw

Cellulases can be used for biofuel production to decrease the fuel crises in the world. Microorganisms cultured on lignocellulosic wastes can be used for the production of cellulolytic enzymes at large scale. In the current study, cellulolytic enzyme production potential of Aspergillus fumigatus was...

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Veröffentlicht in:Applied biochemistry and biotechnology 2014-04, Vol.172 (7), p.3646-3655
Hauptverfasser: Mehboob, Nazia, Asad, M. Javaid, Asgher, M, Gulfraz, M, Mukhtar, Tariq, Mahmood, Raja Tahir
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container_issue 7
container_start_page 3646
container_title Applied biochemistry and biotechnology
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creator Mehboob, Nazia
Asad, M. Javaid
Asgher, M
Gulfraz, M
Mukhtar, Tariq
Mahmood, Raja Tahir
description Cellulases can be used for biofuel production to decrease the fuel crises in the world. Microorganisms cultured on lignocellulosic wastes can be used for the production of cellulolytic enzymes at large scale. In the current study, cellulolytic enzyme production potential of Aspergillus fumigatus was explored and optimized by employing various cultural and nutritional parameters. Maximum endoglucanase production was observed after 72 h at 55 °C, pH 5.5, and 70 % moisture level. Addition of 0.3 % of fructose, peptone, and Tween-80 further enhanced the production of endoglucanase. Maximum purification was achieved with 40 % ammonium sulfate, and it was purified 2.63-fold by gel filtration chromatography. Endoglucanase has 55 °C optimum temperature, 4.8 optimum pH, 3.97 mM K ₘ, and 8.53 μM/mL/min V ₘₐₓ. Maximum exoglucanase production was observed at 55 °C after 72 h, at pH 5.5, and 70 % moisture level. Further addition of 0.3 % of each of fructose, peptone, and Tween-80 enhances the secretion of endoglucanase. It was purified 3.30-fold in the presence of 40 % ammonium sulfate followed by gel filtration chromatography. Its optimum temperature was 55 °C, optimum pH was 4.8, 4.34 mM K ₘ, and 7.29 μM/mL/min V ₘₐₓ. In the case of β-glucosidase, maximum activity was observed after 72 h at 55 °C, pH 5.5, and 70 % moisture level. The presence of 0.3 % of fructose, peptone, and Tween-80 in media has beneficial impact on β-glucosidase production. A 4.36-fold purification was achieved by 40 % ammonium sulfate precipitation and gel filtration chromatography. Optimum temperature of β-glucosidase was 55 °C, optimum pH was 4.8, K ₘ was 4.92 mM, and V ₘₐₓ 6.75 μM/mL/min. It was also observed that fructose is better than glucose, and peptone is better than urea for the growth of A. fumigatus. The K ₘ and V ₘₐₓ values indicated that endoglucanase, exoglucanase, and β-glucosidase have good affinity for their substrates.
doi_str_mv 10.1007/s12010-014-0796-3
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Javaid ; Asgher, M ; Gulfraz, M ; Mukhtar, Tariq ; Mahmood, Raja Tahir</creator><creatorcontrib>Mehboob, Nazia ; Asad, M. Javaid ; Asgher, M ; Gulfraz, M ; Mukhtar, Tariq ; Mahmood, Raja Tahir</creatorcontrib><description>Cellulases can be used for biofuel production to decrease the fuel crises in the world. Microorganisms cultured on lignocellulosic wastes can be used for the production of cellulolytic enzymes at large scale. In the current study, cellulolytic enzyme production potential of Aspergillus fumigatus was explored and optimized by employing various cultural and nutritional parameters. Maximum endoglucanase production was observed after 72 h at 55 °C, pH 5.5, and 70 % moisture level. Addition of 0.3 % of fructose, peptone, and Tween-80 further enhanced the production of endoglucanase. Maximum purification was achieved with 40 % ammonium sulfate, and it was purified 2.63-fold by gel filtration chromatography. Endoglucanase has 55 °C optimum temperature, 4.8 optimum pH, 3.97 mM K ₘ, and 8.53 μM/mL/min V ₘₐₓ. Maximum exoglucanase production was observed at 55 °C after 72 h, at pH 5.5, and 70 % moisture level. Further addition of 0.3 % of each of fructose, peptone, and Tween-80 enhances the secretion of endoglucanase. It was purified 3.30-fold in the presence of 40 % ammonium sulfate followed by gel filtration chromatography. Its optimum temperature was 55 °C, optimum pH was 4.8, 4.34 mM K ₘ, and 7.29 μM/mL/min V ₘₐₓ. In the case of β-glucosidase, maximum activity was observed after 72 h at 55 °C, pH 5.5, and 70 % moisture level. The presence of 0.3 % of fructose, peptone, and Tween-80 in media has beneficial impact on β-glucosidase production. A 4.36-fold purification was achieved by 40 % ammonium sulfate precipitation and gel filtration chromatography. Optimum temperature of β-glucosidase was 55 °C, optimum pH was 4.8, K ₘ was 4.92 mM, and V ₘₐₓ 6.75 μM/mL/min. 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Psychology ; Fungal Proteins - chemistry ; Fungal Proteins - genetics ; glucose ; Hot Temperature ; Industrial Microbiology - instrumentation ; Industrial Microbiology - methods ; lignocellulosic wastes ; Methods. Procedures. Technologies ; Microbial engineering. Fermentation and microbial culture technology ; Microorganisms ; Peptones ; Plant Stems - metabolism ; Plant Stems - microbiology ; secretion ; size exclusion chromatography ; solid state fermentation ; Sulfates ; temperature ; Triticum - metabolism ; Triticum - microbiology ; Triticum aestivum ; Urea ; Wheat ; Wheat straw</subject><ispartof>Applied biochemistry and biotechnology, 2014-04, Vol.172 (7), p.3646-3655</ispartof><rights>Springer Science+Business Media New York 2014</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c459t-c7eb28dbd20eca44ed8a0a35066dd68457087c0bef99963fb4c011a039bf2f9b3</citedby><cites>FETCH-LOGICAL-c459t-c7eb28dbd20eca44ed8a0a35066dd68457087c0bef99963fb4c011a039bf2f9b3</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/s12010-014-0796-3$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12010-014-0796-3$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=28575622$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24562980$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mehboob, Nazia</creatorcontrib><creatorcontrib>Asad, M. Javaid</creatorcontrib><creatorcontrib>Asgher, M</creatorcontrib><creatorcontrib>Gulfraz, M</creatorcontrib><creatorcontrib>Mukhtar, Tariq</creatorcontrib><creatorcontrib>Mahmood, Raja Tahir</creatorcontrib><title>Exploring Thermophilic Cellulolytic Enzyme Production Potential of Aspergillus fumigatus by the Solid-State Fermentation of Wheat Straw</title><title>Applied biochemistry and biotechnology</title><addtitle>Appl Biochem Biotechnol</addtitle><addtitle>Appl Biochem Biotechnol</addtitle><description>Cellulases can be used for biofuel production to decrease the fuel crises in the world. Microorganisms cultured on lignocellulosic wastes can be used for the production of cellulolytic enzymes at large scale. In the current study, cellulolytic enzyme production potential of Aspergillus fumigatus was explored and optimized by employing various cultural and nutritional parameters. Maximum endoglucanase production was observed after 72 h at 55 °C, pH 5.5, and 70 % moisture level. Addition of 0.3 % of fructose, peptone, and Tween-80 further enhanced the production of endoglucanase. Maximum purification was achieved with 40 % ammonium sulfate, and it was purified 2.63-fold by gel filtration chromatography. Endoglucanase has 55 °C optimum temperature, 4.8 optimum pH, 3.97 mM K ₘ, and 8.53 μM/mL/min V ₘₐₓ. Maximum exoglucanase production was observed at 55 °C after 72 h, at pH 5.5, and 70 % moisture level. Further addition of 0.3 % of each of fructose, peptone, and Tween-80 enhances the secretion of endoglucanase. It was purified 3.30-fold in the presence of 40 % ammonium sulfate followed by gel filtration chromatography. Its optimum temperature was 55 °C, optimum pH was 4.8, 4.34 mM K ₘ, and 7.29 μM/mL/min V ₘₐₓ. In the case of β-glucosidase, maximum activity was observed after 72 h at 55 °C, pH 5.5, and 70 % moisture level. The presence of 0.3 % of fructose, peptone, and Tween-80 in media has beneficial impact on β-glucosidase production. A 4.36-fold purification was achieved by 40 % ammonium sulfate precipitation and gel filtration chromatography. Optimum temperature of β-glucosidase was 55 °C, optimum pH was 4.8, K ₘ was 4.92 mM, and V ₘₐₓ 6.75 μM/mL/min. It was also observed that fructose is better than glucose, and peptone is better than urea for the growth of A. fumigatus. The K ₘ and V ₘₐₓ values indicated that endoglucanase, exoglucanase, and β-glucosidase have good affinity for their substrates.</description><subject>Ammonium</subject><subject>ammonium sulfate</subject><subject>Aspergillus fumigatus</subject><subject>Aspergillus fumigatus - enzymology</subject><subject>Aspergillus fumigatus - metabolism</subject><subject>beta-glucosidase</subject><subject>Biochemistry</subject><subject>Biofuels</subject><subject>Biological and medical sciences</subject><subject>Biomass</subject><subject>Biotechnology</subject><subject>Cellulase - chemistry</subject><subject>Cellulase - genetics</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chromatography</subject><subject>Culture Media - metabolism</subject><subject>endo-1,4-beta-glucanase</subject><subject>Enzyme Stability</subject><subject>Enzymes</subject><subject>Fermentation</subject><subject>Filtration</subject><subject>fructose</subject><subject>fuels</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fungal Proteins - chemistry</subject><subject>Fungal Proteins - genetics</subject><subject>glucose</subject><subject>Hot Temperature</subject><subject>Industrial Microbiology - instrumentation</subject><subject>Industrial Microbiology - methods</subject><subject>lignocellulosic wastes</subject><subject>Methods. Procedures. Technologies</subject><subject>Microbial engineering. Fermentation and microbial culture technology</subject><subject>Microorganisms</subject><subject>Peptones</subject><subject>Plant Stems - metabolism</subject><subject>Plant Stems - microbiology</subject><subject>secretion</subject><subject>size exclusion chromatography</subject><subject>solid state fermentation</subject><subject>Sulfates</subject><subject>temperature</subject><subject>Triticum - metabolism</subject><subject>Triticum - microbiology</subject><subject>Triticum aestivum</subject><subject>Urea</subject><subject>Wheat</subject><subject>Wheat straw</subject><issn>0273-2289</issn><issn>1559-0291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkV1rFDEUhoModlv9Ad5oQArejJ4kk5nJZVm2KhQsbIuXIZPJ7KZkJmOSoa5_wL9ttrt-4IV4lQSe9z05PAi9IPCWANTvIqFAoABSFlCLqmCP0IJwLgqggjxGC6A1KyhtxAk6jfEOgNCG10_RCS15RUUDC_R99XVyPthxg2-2Jgx-2lpnNV4a52bn3S7lx2r8thsMvg6-m3WyfsTXPpkxWeWw7_FFnEzY2ByIuJ8Hu1Ep39odTluD197ZrlgnlQy-zANyTD1U5ODnrVEJr1NQ98_Qk165aJ4fzzN0e7m6WX4orj69_7i8uCp0yUUqdG1a2nRtR8FoVZamaxQoxqGquq5qSl5DU2toTS-EqFjflhoIUcBE29NetOwMvTn0TsF_mU1McrBR52XVaPwcJeEUWC24EP-BkqpmAIJn9PVf6J2fw5gXeaByY8n2heRA6eBjDKaXU7CDCjtJQO6FyoNQmYXKvVDJcublsXluB9P9Svw0mIHzI6CiVq4PatQ2_uay8EzSzNEDF6e9bRP--OI_pr86hHrlpdqEXHy7zlAJAA1vKGE_ADjSwtM</recordid><startdate>20140401</startdate><enddate>20140401</enddate><creator>Mehboob, Nazia</creator><creator>Asad, M. 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Javaid ; Asgher, M ; Gulfraz, M ; Mukhtar, Tariq ; Mahmood, Raja Tahir</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c459t-c7eb28dbd20eca44ed8a0a35066dd68457087c0bef99963fb4c011a039bf2f9b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Ammonium</topic><topic>ammonium sulfate</topic><topic>Aspergillus fumigatus</topic><topic>Aspergillus fumigatus - enzymology</topic><topic>Aspergillus fumigatus - metabolism</topic><topic>beta-glucosidase</topic><topic>Biochemistry</topic><topic>Biofuels</topic><topic>Biological and medical sciences</topic><topic>Biomass</topic><topic>Biotechnology</topic><topic>Cellulase - chemistry</topic><topic>Cellulase - genetics</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chromatography</topic><topic>Culture Media - metabolism</topic><topic>endo-1,4-beta-glucanase</topic><topic>Enzyme Stability</topic><topic>Enzymes</topic><topic>Fermentation</topic><topic>Filtration</topic><topic>fructose</topic><topic>fuels</topic><topic>Fundamental and applied biological sciences. 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In the current study, cellulolytic enzyme production potential of Aspergillus fumigatus was explored and optimized by employing various cultural and nutritional parameters. Maximum endoglucanase production was observed after 72 h at 55 °C, pH 5.5, and 70 % moisture level. Addition of 0.3 % of fructose, peptone, and Tween-80 further enhanced the production of endoglucanase. Maximum purification was achieved with 40 % ammonium sulfate, and it was purified 2.63-fold by gel filtration chromatography. Endoglucanase has 55 °C optimum temperature, 4.8 optimum pH, 3.97 mM K ₘ, and 8.53 μM/mL/min V ₘₐₓ. Maximum exoglucanase production was observed at 55 °C after 72 h, at pH 5.5, and 70 % moisture level. Further addition of 0.3 % of each of fructose, peptone, and Tween-80 enhances the secretion of endoglucanase. It was purified 3.30-fold in the presence of 40 % ammonium sulfate followed by gel filtration chromatography. Its optimum temperature was 55 °C, optimum pH was 4.8, 4.34 mM K ₘ, and 7.29 μM/mL/min V ₘₐₓ. In the case of β-glucosidase, maximum activity was observed after 72 h at 55 °C, pH 5.5, and 70 % moisture level. The presence of 0.3 % of fructose, peptone, and Tween-80 in media has beneficial impact on β-glucosidase production. A 4.36-fold purification was achieved by 40 % ammonium sulfate precipitation and gel filtration chromatography. Optimum temperature of β-glucosidase was 55 °C, optimum pH was 4.8, K ₘ was 4.92 mM, and V ₘₐₓ 6.75 μM/mL/min. It was also observed that fructose is better than glucose, and peptone is better than urea for the growth of A. fumigatus. The K ₘ and V ₘₐₓ values indicated that endoglucanase, exoglucanase, and β-glucosidase have good affinity for their substrates.</abstract><cop>Boston</cop><pub>Springer-Verlag</pub><pmid>24562980</pmid><doi>10.1007/s12010-014-0796-3</doi><tpages>10</tpages></addata></record>
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subjects Ammonium
ammonium sulfate
Aspergillus fumigatus
Aspergillus fumigatus - enzymology
Aspergillus fumigatus - metabolism
beta-glucosidase
Biochemistry
Biofuels
Biological and medical sciences
Biomass
Biotechnology
Cellulase - chemistry
Cellulase - genetics
Chemistry
Chemistry and Materials Science
Chromatography
Culture Media - metabolism
endo-1,4-beta-glucanase
Enzyme Stability
Enzymes
Fermentation
Filtration
fructose
fuels
Fundamental and applied biological sciences. Psychology
Fungal Proteins - chemistry
Fungal Proteins - genetics
glucose
Hot Temperature
Industrial Microbiology - instrumentation
Industrial Microbiology - methods
lignocellulosic wastes
Methods. Procedures. Technologies
Microbial engineering. Fermentation and microbial culture technology
Microorganisms
Peptones
Plant Stems - metabolism
Plant Stems - microbiology
secretion
size exclusion chromatography
solid state fermentation
Sulfates
temperature
Triticum - metabolism
Triticum - microbiology
Triticum aestivum
Urea
Wheat
Wheat straw
title Exploring Thermophilic Cellulolytic Enzyme Production Potential of Aspergillus fumigatus by the Solid-State Fermentation of Wheat Straw
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