TJNPR 2017
DOI: 10.26538/tjnpr/v1i4.9
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Fruit Wastes as Substrate For the Production of Amylase by Aspergillus niger

Abstract: Waste generation demands that measures must be put in place in order to avert their detrimental effect to the environment. Bioconversion of agricultural waste to useful products like enzyme is a welcome development. Amylase production by Aspergillus niger via submerged fermentation of fruit wastes such as pineapple, orange, banana, cucumber and watermelon was investigated. Biomass of A. niger, amylase produced and pH of the fermenting fruit waste media were determined using standard techniques during submerged… Show more

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Cited by 8 publications
(9 citation statements)
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“…nitrogen source gave the highest yield of biomass and lipase by A. niger in submerged fermentation (George-Okafor et al, 2013;Mishra et al, 2016;Oshoma et al, 2017). Thus, confirming our findings that medium supplemented with (NH ) SO enhanced fungal growth which in turn,…”
Section: Discussionsupporting
confidence: 90%
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“…nitrogen source gave the highest yield of biomass and lipase by A. niger in submerged fermentation (George-Okafor et al, 2013;Mishra et al, 2016;Oshoma et al, 2017). Thus, confirming our findings that medium supplemented with (NH ) SO enhanced fungal growth which in turn,…”
Section: Discussionsupporting
confidence: 90%
“…Nitrogen is the main building block of proteins (enzyme) and is one of the main constituents of living organisms. Supplementation of nitrogen is used to optimize the nitrogen requirement of most microbial species especially fungi (Oshoma et al, 2017). The ability of the various nitrogen sources mostly ammonium sulphate to support POME as a substrate to increase fungal growth confirmed the substrate to be a suitable medium for fungal growth and metabolite production (Costa et al, 2017).…”
Section: Discussionmentioning
confidence: 99%
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“…The fungal isolate was identified based on cultural and microscopy characterization following standard methods and maintained on potato dextrose agar (PDA) slant and stored at 4 o C. Inoculum was prepared from a subculture of Aspergillus niger on PDA plates and incubated for 5 d. After the inoculation period, a solution of 1 % tween 80 was prepared and 10 ml of the solution was poured each time onto the cultured agar plate and the spores was gently scrapped using sterile glass rod. The number of spores was counted using haemocytometer and inoculum size of 10 6 spores/ml was used to inoculate all the media [18,19].…”
Section: Aspergillus Nigermentioning
confidence: 99%
“…o C for 15 mins, cooled and inoculated with 1ml ( 106 spores/ml) from the homogenate Aspergillus niger culture aseptically transferred into each medium [19]. Parameters analyzed at every 2 d interval were citric acid concentration, fungal biomass and pH.…”
Section: All Flask Containing Prepared Medium Was Sterilized At 121mentioning
confidence: 99%