Lipolytic production from solid-state fermentation of the filamentous fungus Penicillium polonicum and its applicability as biocatalyst in the synthesis of ethyl oleate

被引:0
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作者
Carvalho J.K. [1 ,2 ]
Krüger C. [1 ]
Silveira M.A.D. [3 ]
Piana P.A. [2 ]
Rodrigues M.L.F. [2 ]
Rosado A.F. [1 ]
da Silva de Lucca R.A. [2 ]
Fagundes-Klen M.R. [2 ]
da Silva E.A. [2 ]
Buzanello C.V. [2 ]
Teleken J.G. [1 ]
Zanella R.A. [2 ]
机构
[1] Department of Engineering and Exact, Federal University of Paraná, PR, Palotina
[2] Engineering and Exact Sciences Center, State University Western Paraná, PR, Toledo
[3] Axe Oncologie, Centre de Recherche du CHU de Québec – Université Laval, Quebec, G1V 4G2, QC
关键词
Biocatalysis; Biotechnology; Petroleum-derived diesel; Sustainability; Enzymes; Lipase;
D O I
10.1007/s11356-024-33007-4
中图分类号
学科分类号
摘要
Lipases represent versatile biocatalysts extensively employed in transesterification reactions for ester production. Ethyl oleate holds significance in biodiesel production, serving as a sustainable alternative to petroleum-derived diesel. In this study, our goal was to prospect lipase and assess its efficacy as a biocatalyst for ethyl oleate synthesis. For quantitative analysis, a base medium supplemented with Rhodamine B, olive oil, and Tween 80 was used. Solid-state fermentation utilized crambe seeds of varying particle sizes and humidity levels as substrates. In the synthesis of ethyl oleate, molar ratios of 1:3, 1:6, and 1:9, along with a total enzymatic activity of 60 U in n-heptane, were utilized at temperatures of 30 °C, 37 °C, and 44 °C. Reactions were conducted in a shaker at 200 rpm for 60 min. As a result, we first identified Penicillium polonicum and employed the method of solid-state fermentation using crambe seeds as a substrate to produce lipase. Our findings revealed heightened lipolytic activity (22.5 Ug−1) after 96 h of fermentation using crambe cake as the substrate. Optimal results were achieved with crambe seeds at a granulometry of 0.6 mm and a fermentation medium humidity of 60%. Additionally, electron microscopy suggested the immobilization of lipase in the substrate, enabling enzyme reuse for up to 4 cycles with 100% enzymatic activity. Subsequently, we conducted applicability tests of biocatalysts for ethyl oleate synthesis, optimizing parameters such as the acid/alcohol molar ratio, temperature, and reaction time. We attained 100% conversion within 30 min at 37 °C, and our results indicated that the molar ratio proportion did not significantly influence the outcome. These findings provide a methodological alternative for the utilization of biocatalysts in ethyl oleate synthesis. © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2024.
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页码:28632 / 28643
页数:11
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