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Enhanced production of pectinase by Aspergillusterreus NCFT 4269.10 using banana peels as substrate
Aspergillus terreus NCFT4269.10 was implemented in solid-state (SSF) and liquid static surface fermentation (LSSF) for biosynthesis of pectinase. Amongst various substrates, like, mustard oil cake, neem oil cake, groundnut oil cake, black gram peels, green gram peels, chickling vetch peels/grass pea...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4724355/ https://www.ncbi.nlm.nih.gov/pubmed/28330106 http://dx.doi.org/10.1007/s13205-015-0353-y |
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author | Sethi, Bijay Kumar Nanda, Prativa Kumari Sahoo, Santilata |
author_facet | Sethi, Bijay Kumar Nanda, Prativa Kumari Sahoo, Santilata |
author_sort | Sethi, Bijay Kumar |
collection | PubMed |
description | Aspergillus terreus NCFT4269.10 was implemented in solid-state (SSF) and liquid static surface fermentation (LSSF) for biosynthesis of pectinase. Amongst various substrates, like, mustard oil cake, neem oil cake, groundnut oil cake, black gram peels, green gram peels, chickling vetch peels/grass pea peels wheat bran, pearl millet residues, finger millet waste, broken rice, banana peels (BP), apple pomace (AP) and orange peels, banana peel (Musa paradisiaca L.; Family: Musaceae) was most suitable for pectinase biosynthesis (LSSF: 400 ± 21.45 Uml(−1); SSF: 6500 ± 1116.21 Ug(−1)). Optimization of process parameters using one-variable-at-a-time method revealed that an initial medium pH of 5.0 at 30 °C and 96 h of incubation along with mannitol, urea, ammonium persulfate and isoleucine have positive influence on pectinase production. Further, K(+) (1 mM), Riboflavin (10 mg 100 ml(−1)) and gibberellic acid (0.025 %, w/v) supported in enhanced pectinase production. Banana peels and AP at a ratio of 9:1, moisture content of 90 % with 2 % inoculum size were suitable combinations for production of pectinase. Similarly, 96 h of soaking time with 0.1 M phosphate buffer (pH 6.5) is essential for pectinase recovery. Purification to electrophoretic homogeneity revealed 1.42 fold purification with 8.08 % yield and a molecular weight of 24.6 kDa. Scaling up of various fermentation parameters and supplementing BP as the substrate for pectinase production with better recovery could make it promising for different industrial exploitation. |
format | Online Article Text |
id | pubmed-4724355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-47243552016-01-25 Enhanced production of pectinase by Aspergillusterreus NCFT 4269.10 using banana peels as substrate Sethi, Bijay Kumar Nanda, Prativa Kumari Sahoo, Santilata 3 Biotech Original Article Aspergillus terreus NCFT4269.10 was implemented in solid-state (SSF) and liquid static surface fermentation (LSSF) for biosynthesis of pectinase. Amongst various substrates, like, mustard oil cake, neem oil cake, groundnut oil cake, black gram peels, green gram peels, chickling vetch peels/grass pea peels wheat bran, pearl millet residues, finger millet waste, broken rice, banana peels (BP), apple pomace (AP) and orange peels, banana peel (Musa paradisiaca L.; Family: Musaceae) was most suitable for pectinase biosynthesis (LSSF: 400 ± 21.45 Uml(−1); SSF: 6500 ± 1116.21 Ug(−1)). Optimization of process parameters using one-variable-at-a-time method revealed that an initial medium pH of 5.0 at 30 °C and 96 h of incubation along with mannitol, urea, ammonium persulfate and isoleucine have positive influence on pectinase production. Further, K(+) (1 mM), Riboflavin (10 mg 100 ml(−1)) and gibberellic acid (0.025 %, w/v) supported in enhanced pectinase production. Banana peels and AP at a ratio of 9:1, moisture content of 90 % with 2 % inoculum size were suitable combinations for production of pectinase. Similarly, 96 h of soaking time with 0.1 M phosphate buffer (pH 6.5) is essential for pectinase recovery. Purification to electrophoretic homogeneity revealed 1.42 fold purification with 8.08 % yield and a molecular weight of 24.6 kDa. Scaling up of various fermentation parameters and supplementing BP as the substrate for pectinase production with better recovery could make it promising for different industrial exploitation. Springer Berlin Heidelberg 2016-01-23 2016-06 /pmc/articles/PMC4724355/ /pubmed/28330106 http://dx.doi.org/10.1007/s13205-015-0353-y Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Sethi, Bijay Kumar Nanda, Prativa Kumari Sahoo, Santilata Enhanced production of pectinase by Aspergillusterreus NCFT 4269.10 using banana peels as substrate |
title | Enhanced production of pectinase by Aspergillusterreus NCFT 4269.10 using banana peels as substrate |
title_full | Enhanced production of pectinase by Aspergillusterreus NCFT 4269.10 using banana peels as substrate |
title_fullStr | Enhanced production of pectinase by Aspergillusterreus NCFT 4269.10 using banana peels as substrate |
title_full_unstemmed | Enhanced production of pectinase by Aspergillusterreus NCFT 4269.10 using banana peels as substrate |
title_short | Enhanced production of pectinase by Aspergillusterreus NCFT 4269.10 using banana peels as substrate |
title_sort | enhanced production of pectinase by aspergillusterreus ncft 4269.10 using banana peels as substrate |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4724355/ https://www.ncbi.nlm.nih.gov/pubmed/28330106 http://dx.doi.org/10.1007/s13205-015-0353-y |
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