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      Lipolytic Enzymes with Hydrolytic and Esterification Activities Produced by Filamentous Fungi Isolated from Decomposition Leaves in an Aquatic Environment

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          Abstract

          Microbial lipases are prominent biocatalysts able to catalyze a wide variety of reactions in aqueous and nonaqueous media. In this work, filamentous fungi isolated from leaves decomposed in an aquatic environment were screened for lipase production with hydrolytic activity and esterification. Agar plates with Tween 20 and Rhodamine B were used for selection, while submerged cultures with olive oil were subsequently used to select 38 filamentous fungi. Trichoderma harzianum, Fusarium solani, Trichoderma harzianum F5, and Penicillium sp. F36 were grown in six different culture media. F. solani presented the highest lipase production (2.37 U/mL) with esterification activity of 0.07 U/mL using medium composed of (g.L −1) KH 2PO 4 1.00, MgSO 4 H 2O 1.123, and CuSO 4 0.06. Supplementation of this culture medium with organic nitrogen sources increased lipase production by 461.3% using tryptone and by 419.4% using yeast extract. Among the vegetable oils from the Amazon region, degummed cotton oil induced lipase production up to 8.14 U/mL. The lipase produced by F. solani F61 has great potential to application in conventional processes and biodiesel production by transesterification of vegetable oils, as well as food industries in the production of fatty acid esters by hydrolysis and esterification.

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          Most cited references50

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          Solid-state fermentation

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            Bacterial lipases: an overview of production, purification and biochemical properties.

            Lipases, triacylglycerol hydrolases, are an important group of biotechnologically relevant enzymes and they find immense applications in food, dairy, detergent and pharmaceutical industries. Lipases are by and large produced from microbes and specifically bacterial lipases play a vital role in commercial ventures. Some important lipase-producing bacterial genera include Bacillus, Pseudomonas and Burkholderia. Lipases are generally produced on lipidic carbon, such as oils, fatty acids, glycerol or tweens in the presence of an organic nitrogen source. Bacterial lipases are mostly extracellular and are produced by submerged fermentation. The enzyme is most commonly purified by hydrophobic interaction chromatography, in addition to some modern approaches such as reverse micellar and aqueous two-phase systems. Most lipases can act in a wide range of pH and temperature, though alkaline bacterial lipases are more common. Lipases are serine hydrolases and have high stability in organic solvents. Besides these, some lipases exhibit chemo-, regio- and enantioselectivity. The latest trend in lipase research is the development of novel and improved lipases through molecular approaches such as directed evolution and exploring natural communities by the metagenomic approach.
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              The Use of Solid Media for Detection of Enzyme Production by Fungi

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                Author and article information

                Contributors
                Journal
                Enzyme Res
                Enzyme Res
                ER
                Enzyme Research
                Hindawi
                2090-0406
                2090-0414
                2019
                2 June 2019
                : 2019
                : 8182425
                Affiliations
                1UFT, Brazil
                2UFT Campus Palmas, Brazil
                3UFT Campus Gurupi, Brazil
                4INPA, Brazil
                Author notes

                Academic Editor: Raffaele Porta

                Author information
                http://orcid.org/0000-0002-2115-9796
                Article
                10.1155/2019/8182425
                6582840
                82a5836e-4af0-417b-814f-b50af56bf63f
                Copyright © 2019 D. B. Mendes et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 19 November 2018
                : 29 March 2019
                : 9 May 2019
                Funding
                Funded by: Federal University of Tocantins and the Postgraduate Program in Biodiversity and Biotechnology
                Funded by: Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
                Award ID: [001]
                Categories
                Research Article

                Biochemistry
                Biochemistry

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