Fungal strain selection for protease production by solid-state fermentation using agro-industrial waste as substrates

被引:0
|
作者
M. A. Lizardi-Jiménez
J. Ricardo-Díaz
T. A. Quiñones-Muñoz
F. Hernández-Rosas
R. Hernández-Martínez
机构
[1] CONACYT,CONACYT–Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco A.C.
[2] Universidad Autónoma de San Luis Potosí,Colegio de Postgraduados
[3] Instituto Tecnológico Superior de Tierra Blanca,Campus Córdoba
[4] Boulevard Circuito La Concepción 3,CONACYT
[5] Carretera Federal Córdoba-Veracruz Km 348, Colegio de Postgraduados
[6] Congregación Manuel León,Campus Córdoba
[7] Municipio Amatlán de los Reyes,undefined
[8] Carretera Federal Córdoba-Veracruz Km 348,undefined
[9] Congregación Manuel León,undefined
[10] Municipio Amatlán de los Reyes,undefined
来源
Chemical Papers | 2019年 / 73卷
关键词
Milk-clotting enzyme; Protease; Solid-state fermentation; Pineapple waste; Agro-industrial wastes; Fungal strains;
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摘要
Screening of the fungal strains, Aspergillus niger, Trichoderma harzianum, and Rhizopus microsporus var. chinensis for protease production was realised by monitoring the presence of clear zones on skimmed milk agar plates. Additionally, screening of the radial growth on vanilla waste, cane bagasse, and pineapple crown plates was performed. Radial growth data of the fungal strains on skimmed milk agar and agro-industrial waste plates were adjusted to the Gompertz model. The results indicate that R. microsporus var. chinensis and pineapple crown were adequate for the production of milk-clotting enzymes by solid-state fermentation. Crude enzyme extract was produced via solid-state fermentation using two particle sizes [2–2.6 mm (SSF1) and a mixture of less than 1 mm with 2–2.6 mm, at a ratio of 1:1(SSF2)]. The highest milk-clotting and proteolytic activities were shown within 12 h and 48 h of fermentation for SSF1 and SSF2, respectively. The optimum milk-clotting activity presented by the crude enzyme extract was at pH 6.5, 40 °C, and 0.04 M CaCl2. The ratio of milk-clotting activity to proteolytic activity (9.7) presented by the crude enzyme extract indicates potential for use as a calf rennet substitute.
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页码:2603 / 2610
页数:7
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