Characterization and Preparation of Aspergillus niger Naringinase for Debittering Citrus Juice

:  Naringinase from Aspergillus niger was prepared and characterized to evaluate its effectiveness in debittering citrus juice. The enzyme was purified to homogeneity by sulfate fractionation and chromatographies on Q‐Sepharose, Sephacryl S‐200, and S‐100 HR columns, and estimated by gel filtration...

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Veröffentlicht in:Journal of food science 2012-01, Vol.77 (1), p.C1-C7
Hauptverfasser: Ni, Hui, Chen, Feng, Cai, Huinong, Xiao, Anfeng, You, Qi, Lu, Yunzhen
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creator Ni, Hui
Chen, Feng
Cai, Huinong
Xiao, Anfeng
You, Qi
Lu, Yunzhen
description :  Naringinase from Aspergillus niger was prepared and characterized to evaluate its effectiveness in debittering citrus juice. The enzyme was purified to homogeneity by sulfate fractionation and chromatographies on Q‐Sepharose, Sephacryl S‐200, and S‐100 HR columns, and estimated by gel filtration chromatography (GFC) to have a molecular weight (MW) of 131 kDa, of which its subunit was measured by sodium dodecyl sulfate‐polyacrylamide gel electrophoresis to be around 65.5 kDa. The enzyme showed active and stable pH ranges both within 4.5 to 5.0. Its optimal temperature was in the range of 45 to 55 °C. Freeze drying provided an estimated enzymatic recovery of 95.9%, greater than spray drying with the recovery at 55.6%. The freeze‐drying powder could retain its enzymatic activity stably at 4 °C for 6 mo. Also, the enzyme in 0.220 U/mL citrus juice could sufficiently remove the naringin for the bitterness. Oral acute toxicity study revealed the maximum tolerated dose (MTD) of the naringinase powder was >10 g/kg in mice. The contents of arsenic (As), lead (Pb), mercury (Hg), the aerobic plate count, and coliform number in the enzyme powder all met the criteria for food use. These characteristics suggest that the naringinase from A. niger is efficient and suitable for debittering the citrus juice, and the process consisting of fermentation, salt precipitation, ion exchange, ultrafiltration, and freeze drying is a promising means to prepare the naringinase for food industry, setting up a strong base to enzymatically debitter citrus juice. Practical Application:  This study focused on characterization, preparation, and validation of naringinase from A. niger, which provided useful information on how to prepare, store, and use the naringinase. In addition, this naringinase met the safety standards for food use and showed strong ability to remove the bitter taste from citrus juice, which provided useful information for interested readers, and the food industry.
doi_str_mv 10.1111/j.1750-3841.2011.02471.x
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The enzyme was purified to homogeneity by sulfate fractionation and chromatographies on Q‐Sepharose, Sephacryl S‐200, and S‐100 HR columns, and estimated by gel filtration chromatography (GFC) to have a molecular weight (MW) of 131 kDa, of which its subunit was measured by sodium dodecyl sulfate‐polyacrylamide gel electrophoresis to be around 65.5 kDa. The enzyme showed active and stable pH ranges both within 4.5 to 5.0. Its optimal temperature was in the range of 45 to 55 °C. Freeze drying provided an estimated enzymatic recovery of 95.9%, greater than spray drying with the recovery at 55.6%. The freeze‐drying powder could retain its enzymatic activity stably at 4 °C for 6 mo. Also, the enzyme in 0.220 U/mL citrus juice could sufficiently remove the naringin for the bitterness. Oral acute toxicity study revealed the maximum tolerated dose (MTD) of the naringinase powder was &gt;10 g/kg in mice. The contents of arsenic (As), lead (Pb), mercury (Hg), the aerobic plate count, and coliform number in the enzyme powder all met the criteria for food use. These characteristics suggest that the naringinase from A. niger is efficient and suitable for debittering the citrus juice, and the process consisting of fermentation, salt precipitation, ion exchange, ultrafiltration, and freeze drying is a promising means to prepare the naringinase for food industry, setting up a strong base to enzymatically debitter citrus juice. Practical Application:  This study focused on characterization, preparation, and validation of naringinase from A. niger, which provided useful information on how to prepare, store, and use the naringinase. 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The enzyme was purified to homogeneity by sulfate fractionation and chromatographies on Q‐Sepharose, Sephacryl S‐200, and S‐100 HR columns, and estimated by gel filtration chromatography (GFC) to have a molecular weight (MW) of 131 kDa, of which its subunit was measured by sodium dodecyl sulfate‐polyacrylamide gel electrophoresis to be around 65.5 kDa. The enzyme showed active and stable pH ranges both within 4.5 to 5.0. Its optimal temperature was in the range of 45 to 55 °C. Freeze drying provided an estimated enzymatic recovery of 95.9%, greater than spray drying with the recovery at 55.6%. The freeze‐drying powder could retain its enzymatic activity stably at 4 °C for 6 mo. Also, the enzyme in 0.220 U/mL citrus juice could sufficiently remove the naringin for the bitterness. Oral acute toxicity study revealed the maximum tolerated dose (MTD) of the naringinase powder was &gt;10 g/kg in mice. The contents of arsenic (As), lead (Pb), mercury (Hg), the aerobic plate count, and coliform number in the enzyme powder all met the criteria for food use. These characteristics suggest that the naringinase from A. niger is efficient and suitable for debittering the citrus juice, and the process consisting of fermentation, salt precipitation, ion exchange, ultrafiltration, and freeze drying is a promising means to prepare the naringinase for food industry, setting up a strong base to enzymatically debitter citrus juice. Practical Application:  This study focused on characterization, preparation, and validation of naringinase from A. niger, which provided useful information on how to prepare, store, and use the naringinase. In addition, this naringinase met the safety standards for food use and showed strong ability to remove the bitter taste from citrus juice, which provided useful information for interested readers, and the food industry.</description><subject>Animals</subject><subject>Aspergillus niger</subject><subject>Aspergillus niger - enzymology</subject><subject>beta-Glucosidase - adverse effects</subject><subject>beta-Glucosidase - chemistry</subject><subject>beta-Glucosidase - isolation &amp; purification</subject><subject>beta-Glucosidase - metabolism</subject><subject>Beverages - analysis</subject><subject>Biological and medical sciences</subject><subject>Citrus</subject><subject>Citrus - chemistry</subject><subject>citrus juice</subject><subject>debittering</subject><subject>Enzyme Stability</subject><subject>Enzymes</subject><subject>Female</subject><subject>Flavanones - metabolism</subject><subject>Flavoring Agents - adverse effects</subject><subject>Flavoring Agents - chemistry</subject><subject>Flavoring Agents - isolation &amp; purification</subject><subject>Flavoring Agents - metabolism</subject><subject>Food industries</subject><subject>Food preservation</subject><subject>Food science</subject><subject>Freeze Drying</subject><subject>Fruit and vegetable industries</subject><subject>Fruit juices</subject><subject>Fundamental and applied biological sciences. 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Psychology</topic><topic>Fungal Proteins - adverse effects</topic><topic>Fungal Proteins - chemistry</topic><topic>Fungal Proteins - isolation &amp; purification</topic><topic>Fungal Proteins - metabolism</topic><topic>Hydrogen-Ion Concentration</topic><topic>Male</topic><topic>Maximum Tolerated Dose</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Molecular Weight</topic><topic>Multienzyme Complexes - adverse effects</topic><topic>Multienzyme Complexes - chemistry</topic><topic>Multienzyme Complexes - isolation &amp; purification</topic><topic>Multienzyme Complexes - metabolism</topic><topic>naringinase</topic><topic>oral acute toxicity</topic><topic>Protein Subunits - adverse effects</topic><topic>Protein Subunits - chemistry</topic><topic>Protein Subunits - isolation &amp; purification</topic><topic>Protein Subunits - metabolism</topic><topic>Taste</topic><topic>Temperature</topic><topic>Toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ni, Hui</creatorcontrib><creatorcontrib>Chen, Feng</creatorcontrib><creatorcontrib>Cai, Huinong</creatorcontrib><creatorcontrib>Xiao, Anfeng</creatorcontrib><creatorcontrib>You, Qi</creatorcontrib><creatorcontrib>Lu, Yunzhen</creatorcontrib><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>Biotechnology Research Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Environment 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>ANTE: Abstracts in New Technology &amp; Engineering</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Journal of food science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ni, Hui</au><au>Chen, Feng</au><au>Cai, Huinong</au><au>Xiao, Anfeng</au><au>You, Qi</au><au>Lu, Yunzhen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization and Preparation of Aspergillus niger Naringinase for Debittering Citrus Juice</atitle><jtitle>Journal of food science</jtitle><addtitle>J Food Sci</addtitle><date>2012-01</date><risdate>2012</risdate><volume>77</volume><issue>1</issue><spage>C1</spage><epage>C7</epage><pages>C1-C7</pages><issn>0022-1147</issn><eissn>1750-3841</eissn><coden>JFDSAZ</coden><abstract>:  Naringinase from Aspergillus niger was prepared and characterized to evaluate its effectiveness in debittering citrus juice. The enzyme was purified to homogeneity by sulfate fractionation and chromatographies on Q‐Sepharose, Sephacryl S‐200, and S‐100 HR columns, and estimated by gel filtration chromatography (GFC) to have a molecular weight (MW) of 131 kDa, of which its subunit was measured by sodium dodecyl sulfate‐polyacrylamide gel electrophoresis to be around 65.5 kDa. The enzyme showed active and stable pH ranges both within 4.5 to 5.0. Its optimal temperature was in the range of 45 to 55 °C. Freeze drying provided an estimated enzymatic recovery of 95.9%, greater than spray drying with the recovery at 55.6%. The freeze‐drying powder could retain its enzymatic activity stably at 4 °C for 6 mo. Also, the enzyme in 0.220 U/mL citrus juice could sufficiently remove the naringin for the bitterness. Oral acute toxicity study revealed the maximum tolerated dose (MTD) of the naringinase powder was &gt;10 g/kg in mice. The contents of arsenic (As), lead (Pb), mercury (Hg), the aerobic plate count, and coliform number in the enzyme powder all met the criteria for food use. These characteristics suggest that the naringinase from A. niger is efficient and suitable for debittering the citrus juice, and the process consisting of fermentation, salt precipitation, ion exchange, ultrafiltration, and freeze drying is a promising means to prepare the naringinase for food industry, setting up a strong base to enzymatically debitter citrus juice. Practical Application:  This study focused on characterization, preparation, and validation of naringinase from A. niger, which provided useful information on how to prepare, store, and use the naringinase. In addition, this naringinase met the safety standards for food use and showed strong ability to remove the bitter taste from citrus juice, which provided useful information for interested readers, and the food industry.</abstract><cop>Malden, USA</cop><pub>Blackwell Publishing Inc</pub><pmid>22122507</pmid><doi>10.1111/j.1750-3841.2011.02471.x</doi><tpages>7</tpages></addata></record>
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subjects Animals
Aspergillus niger
Aspergillus niger - enzymology
beta-Glucosidase - adverse effects
beta-Glucosidase - chemistry
beta-Glucosidase - isolation & purification
beta-Glucosidase - metabolism
Beverages - analysis
Biological and medical sciences
Citrus
Citrus - chemistry
citrus juice
debittering
Enzyme Stability
Enzymes
Female
Flavanones - metabolism
Flavoring Agents - adverse effects
Flavoring Agents - chemistry
Flavoring Agents - isolation & purification
Flavoring Agents - metabolism
Food industries
Food preservation
Food science
Freeze Drying
Fruit and vegetable industries
Fruit juices
Fundamental and applied biological sciences. Psychology
Fungal Proteins - adverse effects
Fungal Proteins - chemistry
Fungal Proteins - isolation & purification
Fungal Proteins - metabolism
Hydrogen-Ion Concentration
Male
Maximum Tolerated Dose
Mice
Mice, Inbred Strains
Molecular Weight
Multienzyme Complexes - adverse effects
Multienzyme Complexes - chemistry
Multienzyme Complexes - isolation & purification
Multienzyme Complexes - metabolism
naringinase
oral acute toxicity
Protein Subunits - adverse effects
Protein Subunits - chemistry
Protein Subunits - isolation & purification
Protein Subunits - metabolism
Taste
Temperature
Toxicity
title Characterization and Preparation of Aspergillus niger Naringinase for Debittering Citrus Juice
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