Extraction, partial purification and characterization of pectinases isolated from Aspergillus species cultured on mango (Mangifera indica) peels

Pectinase was produced from a culture of Aspergillus niger, Aspergillus fumigatus and Aspergillus flavus. Pectinase synthesis was achieved using mango (Mangifera indica) pectin extract as an inducer during pectinolytic fungi isolation while submerged fermentation process was carried out using ground...

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Veröffentlicht in:African journal of biotechnology 2014-06, Vol.13 (24), p.2445-2454
Hauptverfasser: Daniel, Ikenna UDENWOBELE, Chukwunonso, Anthony NSUDE, Arinze, Linus EZUGWU, Sabinus, Oscar Onyebuchi EZE, Chukwudi, ANYAWU, Peter, Nzemndu UZOEGWU, Ferdinand, Chiemeka CHILAKA
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container_issue 24
container_start_page 2445
container_title African journal of biotechnology
container_volume 13
creator Daniel, Ikenna UDENWOBELE
Chukwunonso, Anthony NSUDE
Arinze, Linus EZUGWU
Sabinus, Oscar Onyebuchi EZE
Chukwudi, ANYAWU
Peter, Nzemndu UZOEGWU
Ferdinand, Chiemeka CHILAKA
description Pectinase was produced from a culture of Aspergillus niger, Aspergillus fumigatus and Aspergillus flavus. Pectinase synthesis was achieved using mango (Mangifera indica) pectin extract as an inducer during pectinolytic fungi isolation while submerged fermentation process was carried out using ground mango peels as the sole carbon source. Substrate fermentation was evaluated within seven days by monitoring the pectinase activity every 24 h. The highest pectinase secretion was obtained from A. niger and A. fumigatus after 92 h (day 4) of incubation, while in A. flavus, it was after 120 h (day 5). Crude enzyme extracts from the three organisms were partially purified by a combination of ammonium sulphate precipitation and dialysis with an approximately two-fold purification of the pectinase and a yield of 5.4, 7.66 and 5.99% for A. niger, A. fumigatus and A. flavus, respectively after dialysis. The specific activities of 1.62, 1.79 and 1.86 U/mg for A. niger, A. fumigatus and A. flavus enzymes were calculated, respectively. Pectinase from A. niger and A. fumigatus had pH and temperature optima of 5.0 and 40[degrees]C, respectively, while that from A. flavus had pH and temperature optima of 5.0 and 45[degrees]C. The Michealis constant, Km and the maximum velocity, Vmax determined from Lineweaver-Burk plots of initial velocity data at different concentrations of the mango pectin extract were 0.357 mg/ml and 35.34 U 0.156 mg/ml and 68.0 U; and 0.261 mg/ml and 60.61 U; for the enzymes from A. niger, A. fumigatus and A. flavus, respectively. The results suggest that mango peels can be used for value added synthesis of pectinase, an important enzyme with numerous biotechnological applications.
doi_str_mv 10.5897/AJB2014.13771
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Pectinase synthesis was achieved using mango (Mangifera indica) pectin extract as an inducer during pectinolytic fungi isolation while submerged fermentation process was carried out using ground mango peels as the sole carbon source. Substrate fermentation was evaluated within seven days by monitoring the pectinase activity every 24 h. The highest pectinase secretion was obtained from A. niger and A. fumigatus after 92 h (day 4) of incubation, while in A. flavus, it was after 120 h (day 5). Crude enzyme extracts from the three organisms were partially purified by a combination of ammonium sulphate precipitation and dialysis with an approximately two-fold purification of the pectinase and a yield of 5.4, 7.66 and 5.99% for A. niger, A. fumigatus and A. flavus, respectively after dialysis. The specific activities of 1.62, 1.79 and 1.86 U/mg for A. niger, A. fumigatus and A. flavus enzymes were calculated, respectively. Pectinase from A. niger and A. fumigatus had pH and temperature optima of 5.0 and 40[degrees]C, respectively, while that from A. flavus had pH and temperature optima of 5.0 and 45[degrees]C. The Michealis constant, Km and the maximum velocity, Vmax determined from Lineweaver-Burk plots of initial velocity data at different concentrations of the mango pectin extract were 0.357 mg/ml and 35.34 U 0.156 mg/ml and 68.0 U; and 0.261 mg/ml and 60.61 U; for the enzymes from A. niger, A. fumigatus and A. flavus, respectively. 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Pectinase from A. niger and A. fumigatus had pH and temperature optima of 5.0 and 40[degrees]C, respectively, while that from A. flavus had pH and temperature optima of 5.0 and 45[degrees]C. The Michealis constant, Km and the maximum velocity, Vmax determined from Lineweaver-Burk plots of initial velocity data at different concentrations of the mango pectin extract were 0.357 mg/ml and 35.34 U 0.156 mg/ml and 68.0 U; and 0.261 mg/ml and 60.61 U; for the enzymes from A. niger, A. fumigatus and A. flavus, respectively. 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Pectinase from A. niger and A. fumigatus had pH and temperature optima of 5.0 and 40[degrees]C, respectively, while that from A. flavus had pH and temperature optima of 5.0 and 45[degrees]C. The Michealis constant, Km and the maximum velocity, Vmax determined from Lineweaver-Burk plots of initial velocity data at different concentrations of the mango pectin extract were 0.357 mg/ml and 35.34 U 0.156 mg/ml and 68.0 U; and 0.261 mg/ml and 60.61 U; for the enzymes from A. niger, A. fumigatus and A. flavus, respectively. The results suggest that mango peels can be used for value added synthesis of pectinase, an important enzyme with numerous biotechnological applications.</abstract><doi>10.5897/AJB2014.13771</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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subjects Aspergillus flavus
Aspergillus fumigatus
Aspergillus niger
Mangifera indica
title Extraction, partial purification and characterization of pectinases isolated from Aspergillus species cultured on mango (Mangifera indica) peels
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