Retracted: Partial purification and characterization of lipase from locally produced edible oil‐seeds and its relevance in industries
Lipase was extracted from germinating seeds of Helianthus annus (Sunflower), Zea mays (Maize), and Brassica compastris (Mustard). The lipolytic activity was assessed using olive oil as substrate at different germination‐time and the maximum‐activity was obtained after 120 hr. Partial‐purification wa...
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description | Lipase was extracted from germinating seeds of Helianthus annus (Sunflower), Zea mays (Maize), and Brassica compastris (Mustard). The lipolytic activity was assessed using olive oil as substrate at different germination‐time and the maximum‐activity was obtained after 120 hr. Partial‐purification was executed by precipitating the seed‐homogenate with varying concentration of ammonium sulfate solution. 80% ammonium sulfate solution showed maximum lipase activity of 5320IUml−1, 3500IUml−1, 3080IUml−1 with 9.6, 6.9, and 4.8‐fold purification and total protein content of 162, 84, and 60 mg for partially purified enzyme extracts namely SN5, BN5, and MN5, respectively. The optimum temperature and pH observed for hydrolysis of olive oil were 37°C, and 8.0 respectively. Enzyme was found to be stable upto 6 days at 4°C and its activity was stimulated by Ca+2ions. Oil‐stains removal from cotton fabric was observed to be superior in the presence of lipase and detergent. Moreover, the SN5, BN5, and MN5 lipase increased free fatty acid release upto 4.2, 4.3, and 3.8 mg, respectively than wastewater without treatment of lipase (0.21 mg) and promoted fat hydrolysis to approximately 40, 42, and 48% mass reduction after 6 hr incubation of fat particle at a concentration of 20 mg/ml. Biodiesel produced by catalyzing transesterification of vegetable oil with SN5, BN5, and MN5 lipase provided an acid value of 0.8, 1.08, and 0.5 mg/g, viscosity 5.50, 5.7, and 5.53 mm2/s and density 0.87, 0.88, and 0.79 g/ml, respectively. To the best of our knowledge, no such study has been conducted prior on lipase from the seeds mentioned above in Azad Kashmir region. |
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The lipolytic activity was assessed using olive oil as substrate at different germination‐time and the maximum‐activity was obtained after 120 hr. Partial‐purification was executed by precipitating the seed‐homogenate with varying concentration of ammonium sulfate solution. 80% ammonium sulfate solution showed maximum lipase activity of 5320IUml−1, 3500IUml−1, 3080IUml−1 with 9.6, 6.9, and 4.8‐fold purification and total protein content of 162, 84, and 60 mg for partially purified enzyme extracts namely SN5, BN5, and MN5, respectively. The optimum temperature and pH observed for hydrolysis of olive oil were 37°C, and 8.0 respectively. Enzyme was found to be stable upto 6 days at 4°C and its activity was stimulated by Ca+2ions. Oil‐stains removal from cotton fabric was observed to be superior in the presence of lipase and detergent. Moreover, the SN5, BN5, and MN5 lipase increased free fatty acid release upto 4.2, 4.3, and 3.8 mg, respectively than wastewater without treatment of lipase (0.21 mg) and promoted fat hydrolysis to approximately 40, 42, and 48% mass reduction after 6 hr incubation of fat particle at a concentration of 20 mg/ml. Biodiesel produced by catalyzing transesterification of vegetable oil with SN5, BN5, and MN5 lipase provided an acid value of 0.8, 1.08, and 0.5 mg/g, viscosity 5.50, 5.7, and 5.53 mm2/s and density 0.87, 0.88, and 0.79 g/ml, respectively. To the best of our knowledge, no such study has been conducted prior on lipase from the seeds mentioned above in Azad Kashmir region.</description><identifier>ISSN: 8756-7938</identifier><identifier>ISSN: 1520-6033</identifier><identifier>EISSN: 1520-6033</identifier><identifier>DOI: 10.1002/btpr.3092</identifier><identifier>PMID: 33058555</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Ammonium ; Ammonium sulfate ; biodiesel ; Biodiesel fuels ; Biofuels ; Brassica ; Cotton ; Edible oils ; Enzymes ; extraction ; Fatty acids ; Germination ; Hydrolysis ; Lipase ; Mustard ; Oilseeds ; Olive oil ; partial purification ; Protein folding ; Protein purification ; Purification ; Seeds ; Substrates ; Sulfates ; Sunflowers ; Transesterification ; Vegetable oils ; wastewater ; Wastewater treatment</subject><ispartof>Biotechnology progress, 2021-01, Vol.37 (1), p.e3092-n/a</ispartof><rights>2020 American Institute of Chemical Engineers</rights><rights>2020 American Institute of Chemical Engineers.</rights><rights>2021 American Institute of Chemical Engineers</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0003-4588-0593</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fbtpr.3092$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fbtpr.3092$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33058555$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Akhter, Kulsoom</creatorcontrib><creatorcontrib>Nazir, Noshad</creatorcontrib><creatorcontrib>Faheem, Aroosa</creatorcontrib><creatorcontrib>Ghous, Tahseen</creatorcontrib><creatorcontrib>Andleeb, Saiqa</creatorcontrib><creatorcontrib>Kiani, Hina Akbar</creatorcontrib><creatorcontrib>Rasheed, Aamir</creatorcontrib><title>Retracted: Partial purification and characterization of lipase from locally produced edible oil‐seeds and its relevance in industries</title><title>Biotechnology progress</title><addtitle>Biotechnol Prog</addtitle><description>Lipase was extracted from germinating seeds of Helianthus annus (Sunflower), Zea mays (Maize), and Brassica compastris (Mustard). The lipolytic activity was assessed using olive oil as substrate at different germination‐time and the maximum‐activity was obtained after 120 hr. Partial‐purification was executed by precipitating the seed‐homogenate with varying concentration of ammonium sulfate solution. 80% ammonium sulfate solution showed maximum lipase activity of 5320IUml−1, 3500IUml−1, 3080IUml−1 with 9.6, 6.9, and 4.8‐fold purification and total protein content of 162, 84, and 60 mg for partially purified enzyme extracts namely SN5, BN5, and MN5, respectively. The optimum temperature and pH observed for hydrolysis of olive oil were 37°C, and 8.0 respectively. Enzyme was found to be stable upto 6 days at 4°C and its activity was stimulated by Ca+2ions. Oil‐stains removal from cotton fabric was observed to be superior in the presence of lipase and detergent. Moreover, the SN5, BN5, and MN5 lipase increased free fatty acid release upto 4.2, 4.3, and 3.8 mg, respectively than wastewater without treatment of lipase (0.21 mg) and promoted fat hydrolysis to approximately 40, 42, and 48% mass reduction after 6 hr incubation of fat particle at a concentration of 20 mg/ml. Biodiesel produced by catalyzing transesterification of vegetable oil with SN5, BN5, and MN5 lipase provided an acid value of 0.8, 1.08, and 0.5 mg/g, viscosity 5.50, 5.7, and 5.53 mm2/s and density 0.87, 0.88, and 0.79 g/ml, respectively. To the best of our knowledge, no such study has been conducted prior on lipase from the seeds mentioned above in Azad Kashmir region.</description><subject>Ammonium</subject><subject>Ammonium sulfate</subject><subject>biodiesel</subject><subject>Biodiesel fuels</subject><subject>Biofuels</subject><subject>Brassica</subject><subject>Cotton</subject><subject>Edible oils</subject><subject>Enzymes</subject><subject>extraction</subject><subject>Fatty acids</subject><subject>Germination</subject><subject>Hydrolysis</subject><subject>Lipase</subject><subject>Mustard</subject><subject>Oilseeds</subject><subject>Olive oil</subject><subject>partial purification</subject><subject>Protein folding</subject><subject>Protein purification</subject><subject>Purification</subject><subject>Seeds</subject><subject>Substrates</subject><subject>Sulfates</subject><subject>Sunflowers</subject><subject>Transesterification</subject><subject>Vegetable oils</subject><subject>wastewater</subject><subject>Wastewater treatment</subject><issn>8756-7938</issn><issn>1520-6033</issn><issn>1520-6033</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp10c9qFTEUBvAgFnutLnwBCbjRxbT5M8kk7rSoLRQspa6HTHKCKbmTMZlRrqvuuvUZfRJz761dCELgQPjxcTgfQi8oOaaEsJNhnvIxJ5o9QisqGGkk4fwxWqlOyKbTXB2ip6XcEEIUkewJOuScCCWEWKG7K5izsTO4t_jS5DmYiKclBx-smUMasRkdtl_NzuTwc_-ZPI5hMgWwz2mNY7Imxg2ecnKLBYfBhSECTiH-vv1VAFzZ5YS54AwRvpvRAg5jfW4pcw5QnqEDb2KB5_fzCH35-OH69Ky5-Pzp_PTdRWOZ5KzhzHI9qI7KVlMtldOmGzwRerBMKOm1UQSoFqAGRRS3VFLvgXeaCCZbyvgRer3Prbt-W6DM_ToUCzGaEdJSetYKWi_T8rbSV__Qm7TksW5XlaZKCqllVW_2yuZUSgbfTzmsTd70lPTbdvptO_22nWpf3icuwxrcg_xbRwUne_AjRNj8P6l_f315tYv8A8yjm4E</recordid><startdate>202101</startdate><enddate>202101</enddate><creator>Akhter, Kulsoom</creator><creator>Nazir, Noshad</creator><creator>Faheem, Aroosa</creator><creator>Ghous, Tahseen</creator><creator>Andleeb, Saiqa</creator><creator>Kiani, Hina Akbar</creator><creator>Rasheed, Aamir</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4588-0593</orcidid></search><sort><creationdate>202101</creationdate><title>Retracted: Partial purification and characterization of lipase from locally produced edible oil‐seeds and its relevance in industries</title><author>Akhter, Kulsoom ; Nazir, Noshad ; Faheem, Aroosa ; Ghous, Tahseen ; Andleeb, Saiqa ; Kiani, Hina Akbar ; Rasheed, Aamir</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2632-32c39b8716491968d9a7bf059bc2586f9a80e195e8b8083c161ffe37905264123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Ammonium</topic><topic>Ammonium sulfate</topic><topic>biodiesel</topic><topic>Biodiesel fuels</topic><topic>Biofuels</topic><topic>Brassica</topic><topic>Cotton</topic><topic>Edible oils</topic><topic>Enzymes</topic><topic>extraction</topic><topic>Fatty acids</topic><topic>Germination</topic><topic>Hydrolysis</topic><topic>Lipase</topic><topic>Mustard</topic><topic>Oilseeds</topic><topic>Olive oil</topic><topic>partial purification</topic><topic>Protein folding</topic><topic>Protein purification</topic><topic>Purification</topic><topic>Seeds</topic><topic>Substrates</topic><topic>Sulfates</topic><topic>Sunflowers</topic><topic>Transesterification</topic><topic>Vegetable oils</topic><topic>wastewater</topic><topic>Wastewater treatment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Akhter, Kulsoom</creatorcontrib><creatorcontrib>Nazir, Noshad</creatorcontrib><creatorcontrib>Faheem, Aroosa</creatorcontrib><creatorcontrib>Ghous, Tahseen</creatorcontrib><creatorcontrib>Andleeb, Saiqa</creatorcontrib><creatorcontrib>Kiani, Hina Akbar</creatorcontrib><creatorcontrib>Rasheed, Aamir</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biotechnology progress</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Akhter, Kulsoom</au><au>Nazir, Noshad</au><au>Faheem, Aroosa</au><au>Ghous, Tahseen</au><au>Andleeb, Saiqa</au><au>Kiani, Hina Akbar</au><au>Rasheed, Aamir</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Retracted: Partial purification and characterization of lipase from locally produced edible oil‐seeds and its relevance in industries</atitle><jtitle>Biotechnology progress</jtitle><addtitle>Biotechnol Prog</addtitle><date>2021-01</date><risdate>2021</risdate><volume>37</volume><issue>1</issue><spage>e3092</spage><epage>n/a</epage><pages>e3092-n/a</pages><issn>8756-7938</issn><issn>1520-6033</issn><eissn>1520-6033</eissn><abstract>Lipase was extracted from germinating seeds of Helianthus annus (Sunflower), Zea mays (Maize), and Brassica compastris (Mustard). The lipolytic activity was assessed using olive oil as substrate at different germination‐time and the maximum‐activity was obtained after 120 hr. Partial‐purification was executed by precipitating the seed‐homogenate with varying concentration of ammonium sulfate solution. 80% ammonium sulfate solution showed maximum lipase activity of 5320IUml−1, 3500IUml−1, 3080IUml−1 with 9.6, 6.9, and 4.8‐fold purification and total protein content of 162, 84, and 60 mg for partially purified enzyme extracts namely SN5, BN5, and MN5, respectively. The optimum temperature and pH observed for hydrolysis of olive oil were 37°C, and 8.0 respectively. Enzyme was found to be stable upto 6 days at 4°C and its activity was stimulated by Ca+2ions. Oil‐stains removal from cotton fabric was observed to be superior in the presence of lipase and detergent. Moreover, the SN5, BN5, and MN5 lipase increased free fatty acid release upto 4.2, 4.3, and 3.8 mg, respectively than wastewater without treatment of lipase (0.21 mg) and promoted fat hydrolysis to approximately 40, 42, and 48% mass reduction after 6 hr incubation of fat particle at a concentration of 20 mg/ml. Biodiesel produced by catalyzing transesterification of vegetable oil with SN5, BN5, and MN5 lipase provided an acid value of 0.8, 1.08, and 0.5 mg/g, viscosity 5.50, 5.7, and 5.53 mm2/s and density 0.87, 0.88, and 0.79 g/ml, respectively. To the best of our knowledge, no such study has been conducted prior on lipase from the seeds mentioned above in Azad Kashmir region.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>33058555</pmid><doi>10.1002/btpr.3092</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-4588-0593</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Ammonium Ammonium sulfate biodiesel Biodiesel fuels Biofuels Brassica Cotton Edible oils Enzymes extraction Fatty acids Germination Hydrolysis Lipase Mustard Oilseeds Olive oil partial purification Protein folding Protein purification Purification Seeds Substrates Sulfates Sunflowers Transesterification Vegetable oils wastewater Wastewater treatment |
title | Retracted: Partial purification and characterization of lipase from locally produced edible oil‐seeds and its relevance in industries |
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