2001
DOI: 10.1016/s1381-1177(00)00244-7
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Screening and catalytic activity in organic synthesis of novel fungal and yeast lipases

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Cited by 91 publications
(71 citation statements)
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“…After autoclaving the medium (121 ºC, 20 min) the mixture was emulsified by vigorous shaking for 15 min, and after cooling to approximately 60 ºC, the medium was transferred to Petri dishes and rapidly cooled. The agar concentration used for the tributyrine assay is in the range suggested by Lawrence (under 1.5%), 29 assuring adequate protein diffusion into the solid medium.…”
Section: Hydrolytic Assaysmentioning
confidence: 99%
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“…After autoclaving the medium (121 ºC, 20 min) the mixture was emulsified by vigorous shaking for 15 min, and after cooling to approximately 60 ºC, the medium was transferred to Petri dishes and rapidly cooled. The agar concentration used for the tributyrine assay is in the range suggested by Lawrence (under 1.5%), 29 assuring adequate protein diffusion into the solid medium.…”
Section: Hydrolytic Assaysmentioning
confidence: 99%
“…23,26,29,32 The initial selection for the detection of a particular activity has a significant weighting in the screening process, since it aims to eliminate the worst candidates and, in general, is carried out through the cultivation of microorganisms in a solid culture medium, in Petri dishes. 44 Triacylglycerides such as triolein or -butyrin are used as standard substrates for the determination of lipase activity.…”
Section: Hydrolytic Screeningmentioning
confidence: 99%
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