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1.
Electron. j. biotechnol ; 43: 1-7, Jan. 2020. tab, graf
Article in English | LILACS | ID: biblio-1087465

ABSTRACT

Background: Biotechnological processes are part of modern industry as well as stricter environmental requirements. The need to reduce production costs and pollution demands for alternatives that involve the integral use of agro-industrial waste to produce bioactive compounds. The citrus industry generates large amounts of wastes due to the destruction of the fruits by microorganisms and insects together with the large amounts of orange waste generated during the production of juice and for sale fresh. The aim of this study was used orange wastes rich in polyphenolic compounds can be used as source carbon of Aspergillus fumigatus MUM 1603 to generate high added value compounds, for example, ellagic acid and other molecules of polyphenolic origin through submerged fermentation system. Results: The orange peel waste had a high concentration of polyphenols, 28% being condensed, 27% ellagitannins, 25% flavonoids and 20% gallotannins. The major polyphenolic compounds were catechin, EA and quercetin. The conditions, using an experimental design of central compounds, that allow the production of the maximum concentration of EA (18.68 mg/g) were found to be: temperature 30°C, inoculum 2 × 107 (spores/g) and orange peel polyphenols 6.2 (g/L). Conclusion: The submerged fermentation process is an effective methodology for the biotransformation of molecules present in orange waste to obtain high value-added as ellagic acid that can be used as powerful antioxidants, antibacterial and other applications.


Subject(s)
Waste Management , Citrus sinensis/chemistry , Ellagic Acid , Aspergillus fumigatus , Waste Products/analysis , Flavonoids/analysis , Biotechnology/methods , Hydrolyzable Tannins/analysis , Fermentation , Polyphenols/analysis , Phytochemicals
2.
Braz. j. microbiol ; 43(3): 1080-1083, July-Sept. 2012. ilus, tab
Article in English | LILACS | ID: lil-656677

ABSTRACT

Use of natural tannin in the screening of tannase producing microbes is really promising. The present work describes about the possibility and integrity of the newly formulated method over the previously reported methods. Tannin isolated from Terminalia belerica Roxb. (Bahera) was used to differentiate between tanninolytic and nontanninolytic microbes. The method is simple, sensitive and superior for the rapid screening and isolation of tannase-producing microbes.


Subject(s)
Plant Structures/enzymology , Fermentation , Tanacetum parthenium/enzymology , Hydrolyzable Tannins/analysis , Hydrolyzable Tannins/isolation & purification , Enzyme Activation , Hydrolysis , Methods
4.
Braz. j. microbiol ; 42(1): 374-387, Jan.-Mar. 2011. ilus, tab
Article in English | LILACS | ID: lil-571412

ABSTRACT

Tannin acyl hydrolase commonly known as tannase is an industrially important enzyme having a wide range of applications, so there is always a scope for novel tannase with better characteristics. A newly isolated tannase-yielding fungal strain identified as Penicillium atramentosum KM was used for tannase production under solid-state fermentation (SSF) using different agro residues like amla (Phyllanthus emblica), ber (Zyzyphus mauritiana), jamun (Syzygium cumini), Jamoa (Eugenia cuspidate) and keekar (Acacia nilotica) leaves. Among these substrates, maximal extracellular tannase production i.e. 170.75 U/gds and 165.56 U/gds was obtained with jamun and keekar leaves respectively at 28ºC after 96 h. A substrate to distilled water ratio of 1:2 (w/v) was found to be the best for tannase production. Supplementation of sodium nitrate (NaNO3) as nitrogen source had enhanced tannase production both in jamun and keekar leaves. Applications of the enzyme were studied in wine clarification and tea cream solubilization. It resulted in 38.05 percent reduction of tannic acid content in case of jamun wine, 43.59 percent reduction in case of grape wine and 74 percent reduction in the tea extract after 3 h at 35ºC.


Subject(s)
Enzyme Activation , Fermentation , Hydrolases/analysis , Penicillium/enzymology , Penicillium/isolation & purification , Hydrolyzable Tannins/analysis , Hydrolyzable Tannins/isolation & purification , Catalysis , Methods , Solubility , Methods
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