Optimization of the production of rhamnolipids by Pseudomonas aeruginosa UFPEDA 614 in solid-state culture
Abstract In recent years, biosurfactants have attracted attention because of their low toxicity, high biodegradability, and good ecological acceptability. However, their production in submerged liquid culture is hampered by the severe foaming that occurs. Solid-state cultivation can avoid this probl...
Ausführliche Beschreibung
Autor*in: |
Camilios Neto, Doumit [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2008 |
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Schlagwörter: |
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Anmerkung: |
© Springer-Verlag 2008 |
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Übergeordnetes Werk: |
Enthalten in: Applied microbiology and biotechnology - Berlin : Springer, 1975, 81(2008), 3 vom: 01. Dez., Seite 441-448 |
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Übergeordnetes Werk: |
volume:81 ; year:2008 ; number:3 ; day:01 ; month:12 ; pages:441-448 |
Links: |
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DOI / URN: |
10.1007/s00253-008-1663-3 |
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Katalog-ID: |
SPR002955601 |
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245 | 1 | 0 | |a Optimization of the production of rhamnolipids by Pseudomonas aeruginosa UFPEDA 614 in solid-state culture |
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520 | |a Abstract In recent years, biosurfactants have attracted attention because of their low toxicity, high biodegradability, and good ecological acceptability. However, their production in submerged liquid culture is hampered by the severe foaming that occurs. Solid-state cultivation can avoid this problem. In the current work, we optimized the production of a rhamnolipid biosurfactant by Pseudomonas aeruginosa UFPEDA 614, grown on a solid medium impregnated with a solution containing glycerol. During the study, we increased the production of the biosurfactant over tenfold, with levels reaching 172 g of rhamnolipid per kilogram of dry initial substrate after 12 days. On the basis of the volume of impregnating solution added to the solid support, this yield is of the order of 46 g/L, which is comparable with the best results that have been obtained to date in submerged liquid cultivation. Our results suggest that there is a great potential for using solid-state cultivation for the production of rhamnolipids. | ||
650 | 4 | |a Rhamnolipids |7 (dpeaa)DE-He213 | |
650 | 4 | |a Biosurfactants |7 (dpeaa)DE-He213 | |
650 | 4 | |a Solid-state cultivation |7 (dpeaa)DE-He213 | |
650 | 4 | |a Solid-state fermentation |7 (dpeaa)DE-He213 | |
700 | 1 | |a Meira, Joel Alexandre |4 aut | |
700 | 1 | |a de Araújo, Janete Magali |4 aut | |
700 | 1 | |a Mitchell, David Alexander |4 aut | |
700 | 1 | |a Krieger, Nadia |4 aut | |
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10.1007/s00253-008-1663-3 doi (DE-627)SPR002955601 (SPR)s00253-008-1663-3-e DE-627 ger DE-627 rakwb eng Camilios Neto, Doumit verfasserin aut Optimization of the production of rhamnolipids by Pseudomonas aeruginosa UFPEDA 614 in solid-state culture 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 2008 Abstract In recent years, biosurfactants have attracted attention because of their low toxicity, high biodegradability, and good ecological acceptability. However, their production in submerged liquid culture is hampered by the severe foaming that occurs. Solid-state cultivation can avoid this problem. In the current work, we optimized the production of a rhamnolipid biosurfactant by Pseudomonas aeruginosa UFPEDA 614, grown on a solid medium impregnated with a solution containing glycerol. During the study, we increased the production of the biosurfactant over tenfold, with levels reaching 172 g of rhamnolipid per kilogram of dry initial substrate after 12 days. On the basis of the volume of impregnating solution added to the solid support, this yield is of the order of 46 g/L, which is comparable with the best results that have been obtained to date in submerged liquid cultivation. Our results suggest that there is a great potential for using solid-state cultivation for the production of rhamnolipids. Rhamnolipids (dpeaa)DE-He213 Biosurfactants (dpeaa)DE-He213 Solid-state cultivation (dpeaa)DE-He213 Solid-state fermentation (dpeaa)DE-He213 Meira, Joel Alexandre aut de Araújo, Janete Magali aut Mitchell, David Alexander aut Krieger, Nadia aut Enthalten in Applied microbiology and biotechnology Berlin : Springer, 1975 81(2008), 3 vom: 01. Dez., Seite 441-448 (DE-627)265509564 (DE-600)1464336-4 1432-0614 nnns volume:81 year:2008 number:3 day:01 month:12 pages:441-448 https://dx.doi.org/10.1007/s00253-008-1663-3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_165 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2110 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 81 2008 3 01 12 441-448 |
spelling |
10.1007/s00253-008-1663-3 doi (DE-627)SPR002955601 (SPR)s00253-008-1663-3-e DE-627 ger DE-627 rakwb eng Camilios Neto, Doumit verfasserin aut Optimization of the production of rhamnolipids by Pseudomonas aeruginosa UFPEDA 614 in solid-state culture 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 2008 Abstract In recent years, biosurfactants have attracted attention because of their low toxicity, high biodegradability, and good ecological acceptability. However, their production in submerged liquid culture is hampered by the severe foaming that occurs. Solid-state cultivation can avoid this problem. In the current work, we optimized the production of a rhamnolipid biosurfactant by Pseudomonas aeruginosa UFPEDA 614, grown on a solid medium impregnated with a solution containing glycerol. During the study, we increased the production of the biosurfactant over tenfold, with levels reaching 172 g of rhamnolipid per kilogram of dry initial substrate after 12 days. On the basis of the volume of impregnating solution added to the solid support, this yield is of the order of 46 g/L, which is comparable with the best results that have been obtained to date in submerged liquid cultivation. Our results suggest that there is a great potential for using solid-state cultivation for the production of rhamnolipids. Rhamnolipids (dpeaa)DE-He213 Biosurfactants (dpeaa)DE-He213 Solid-state cultivation (dpeaa)DE-He213 Solid-state fermentation (dpeaa)DE-He213 Meira, Joel Alexandre aut de Araújo, Janete Magali aut Mitchell, David Alexander aut Krieger, Nadia aut Enthalten in Applied microbiology and biotechnology Berlin : Springer, 1975 81(2008), 3 vom: 01. Dez., Seite 441-448 (DE-627)265509564 (DE-600)1464336-4 1432-0614 nnns volume:81 year:2008 number:3 day:01 month:12 pages:441-448 https://dx.doi.org/10.1007/s00253-008-1663-3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_165 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2110 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 81 2008 3 01 12 441-448 |
allfields_unstemmed |
10.1007/s00253-008-1663-3 doi (DE-627)SPR002955601 (SPR)s00253-008-1663-3-e DE-627 ger DE-627 rakwb eng Camilios Neto, Doumit verfasserin aut Optimization of the production of rhamnolipids by Pseudomonas aeruginosa UFPEDA 614 in solid-state culture 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 2008 Abstract In recent years, biosurfactants have attracted attention because of their low toxicity, high biodegradability, and good ecological acceptability. However, their production in submerged liquid culture is hampered by the severe foaming that occurs. Solid-state cultivation can avoid this problem. In the current work, we optimized the production of a rhamnolipid biosurfactant by Pseudomonas aeruginosa UFPEDA 614, grown on a solid medium impregnated with a solution containing glycerol. During the study, we increased the production of the biosurfactant over tenfold, with levels reaching 172 g of rhamnolipid per kilogram of dry initial substrate after 12 days. On the basis of the volume of impregnating solution added to the solid support, this yield is of the order of 46 g/L, which is comparable with the best results that have been obtained to date in submerged liquid cultivation. Our results suggest that there is a great potential for using solid-state cultivation for the production of rhamnolipids. Rhamnolipids (dpeaa)DE-He213 Biosurfactants (dpeaa)DE-He213 Solid-state cultivation (dpeaa)DE-He213 Solid-state fermentation (dpeaa)DE-He213 Meira, Joel Alexandre aut de Araújo, Janete Magali aut Mitchell, David Alexander aut Krieger, Nadia aut Enthalten in Applied microbiology and biotechnology Berlin : Springer, 1975 81(2008), 3 vom: 01. Dez., Seite 441-448 (DE-627)265509564 (DE-600)1464336-4 1432-0614 nnns volume:81 year:2008 number:3 day:01 month:12 pages:441-448 https://dx.doi.org/10.1007/s00253-008-1663-3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_165 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2110 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 81 2008 3 01 12 441-448 |
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10.1007/s00253-008-1663-3 doi (DE-627)SPR002955601 (SPR)s00253-008-1663-3-e DE-627 ger DE-627 rakwb eng Camilios Neto, Doumit verfasserin aut Optimization of the production of rhamnolipids by Pseudomonas aeruginosa UFPEDA 614 in solid-state culture 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 2008 Abstract In recent years, biosurfactants have attracted attention because of their low toxicity, high biodegradability, and good ecological acceptability. However, their production in submerged liquid culture is hampered by the severe foaming that occurs. Solid-state cultivation can avoid this problem. In the current work, we optimized the production of a rhamnolipid biosurfactant by Pseudomonas aeruginosa UFPEDA 614, grown on a solid medium impregnated with a solution containing glycerol. During the study, we increased the production of the biosurfactant over tenfold, with levels reaching 172 g of rhamnolipid per kilogram of dry initial substrate after 12 days. On the basis of the volume of impregnating solution added to the solid support, this yield is of the order of 46 g/L, which is comparable with the best results that have been obtained to date in submerged liquid cultivation. Our results suggest that there is a great potential for using solid-state cultivation for the production of rhamnolipids. Rhamnolipids (dpeaa)DE-He213 Biosurfactants (dpeaa)DE-He213 Solid-state cultivation (dpeaa)DE-He213 Solid-state fermentation (dpeaa)DE-He213 Meira, Joel Alexandre aut de Araújo, Janete Magali aut Mitchell, David Alexander aut Krieger, Nadia aut Enthalten in Applied microbiology and biotechnology Berlin : Springer, 1975 81(2008), 3 vom: 01. Dez., Seite 441-448 (DE-627)265509564 (DE-600)1464336-4 1432-0614 nnns volume:81 year:2008 number:3 day:01 month:12 pages:441-448 https://dx.doi.org/10.1007/s00253-008-1663-3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_165 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2110 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 81 2008 3 01 12 441-448 |
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Enthalten in Applied microbiology and biotechnology 81(2008), 3 vom: 01. Dez., Seite 441-448 volume:81 year:2008 number:3 day:01 month:12 pages:441-448 |
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Enthalten in Applied microbiology and biotechnology 81(2008), 3 vom: 01. Dez., Seite 441-448 volume:81 year:2008 number:3 day:01 month:12 pages:441-448 |
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Camilios Neto, Doumit @@aut@@ Meira, Joel Alexandre @@aut@@ de Araújo, Janete Magali @@aut@@ Mitchell, David Alexander @@aut@@ Krieger, Nadia @@aut@@ |
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Camilios Neto, Doumit misc Rhamnolipids misc Biosurfactants misc Solid-state cultivation misc Solid-state fermentation Optimization of the production of rhamnolipids by Pseudomonas aeruginosa UFPEDA 614 in solid-state culture |
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Optimization of the production of rhamnolipids by Pseudomonas aeruginosa UFPEDA 614 in solid-state culture Rhamnolipids (dpeaa)DE-He213 Biosurfactants (dpeaa)DE-He213 Solid-state cultivation (dpeaa)DE-He213 Solid-state fermentation (dpeaa)DE-He213 |
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Optimization of the production of rhamnolipids by Pseudomonas aeruginosa UFPEDA 614 in solid-state culture |
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Optimization of the production of rhamnolipids by Pseudomonas aeruginosa UFPEDA 614 in solid-state culture |
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optimization of the production of rhamnolipids by pseudomonas aeruginosa ufpeda 614 in solid-state culture |
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Optimization of the production of rhamnolipids by Pseudomonas aeruginosa UFPEDA 614 in solid-state culture |
abstract |
Abstract In recent years, biosurfactants have attracted attention because of their low toxicity, high biodegradability, and good ecological acceptability. However, their production in submerged liquid culture is hampered by the severe foaming that occurs. Solid-state cultivation can avoid this problem. In the current work, we optimized the production of a rhamnolipid biosurfactant by Pseudomonas aeruginosa UFPEDA 614, grown on a solid medium impregnated with a solution containing glycerol. During the study, we increased the production of the biosurfactant over tenfold, with levels reaching 172 g of rhamnolipid per kilogram of dry initial substrate after 12 days. On the basis of the volume of impregnating solution added to the solid support, this yield is of the order of 46 g/L, which is comparable with the best results that have been obtained to date in submerged liquid cultivation. Our results suggest that there is a great potential for using solid-state cultivation for the production of rhamnolipids. © Springer-Verlag 2008 |
abstractGer |
Abstract In recent years, biosurfactants have attracted attention because of their low toxicity, high biodegradability, and good ecological acceptability. However, their production in submerged liquid culture is hampered by the severe foaming that occurs. Solid-state cultivation can avoid this problem. In the current work, we optimized the production of a rhamnolipid biosurfactant by Pseudomonas aeruginosa UFPEDA 614, grown on a solid medium impregnated with a solution containing glycerol. During the study, we increased the production of the biosurfactant over tenfold, with levels reaching 172 g of rhamnolipid per kilogram of dry initial substrate after 12 days. On the basis of the volume of impregnating solution added to the solid support, this yield is of the order of 46 g/L, which is comparable with the best results that have been obtained to date in submerged liquid cultivation. Our results suggest that there is a great potential for using solid-state cultivation for the production of rhamnolipids. © Springer-Verlag 2008 |
abstract_unstemmed |
Abstract In recent years, biosurfactants have attracted attention because of their low toxicity, high biodegradability, and good ecological acceptability. However, their production in submerged liquid culture is hampered by the severe foaming that occurs. Solid-state cultivation can avoid this problem. In the current work, we optimized the production of a rhamnolipid biosurfactant by Pseudomonas aeruginosa UFPEDA 614, grown on a solid medium impregnated with a solution containing glycerol. During the study, we increased the production of the biosurfactant over tenfold, with levels reaching 172 g of rhamnolipid per kilogram of dry initial substrate after 12 days. On the basis of the volume of impregnating solution added to the solid support, this yield is of the order of 46 g/L, which is comparable with the best results that have been obtained to date in submerged liquid cultivation. Our results suggest that there is a great potential for using solid-state cultivation for the production of rhamnolipids. © Springer-Verlag 2008 |
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Optimization of the production of rhamnolipids by Pseudomonas aeruginosa UFPEDA 614 in solid-state culture |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">SPR002955601</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230519145253.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">201001s2008 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s00253-008-1663-3</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)SPR002955601</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(SPR)s00253-008-1663-3-e</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Camilios Neto, Doumit</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Optimization of the production of rhamnolipids by Pseudomonas aeruginosa UFPEDA 614 in solid-state culture</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2008</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">© Springer-Verlag 2008</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract In recent years, biosurfactants have attracted attention because of their low toxicity, high biodegradability, and good ecological acceptability. However, their production in submerged liquid culture is hampered by the severe foaming that occurs. Solid-state cultivation can avoid this problem. In the current work, we optimized the production of a rhamnolipid biosurfactant by Pseudomonas aeruginosa UFPEDA 614, grown on a solid medium impregnated with a solution containing glycerol. During the study, we increased the production of the biosurfactant over tenfold, with levels reaching 172 g of rhamnolipid per kilogram of dry initial substrate after 12 days. On the basis of the volume of impregnating solution added to the solid support, this yield is of the order of 46 g/L, which is comparable with the best results that have been obtained to date in submerged liquid cultivation. Our results suggest that there is a great potential for using solid-state cultivation for the production of rhamnolipids.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Rhamnolipids</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Biosurfactants</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Solid-state cultivation</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Solid-state fermentation</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Meira, Joel Alexandre</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">de Araújo, Janete Magali</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Mitchell, David Alexander</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Krieger, Nadia</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Applied microbiology and biotechnology</subfield><subfield code="d">Berlin : Springer, 1975</subfield><subfield code="g">81(2008), 3 vom: 01. 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