Aguilar Cristóbal Noé, Favela-Torres Ernesto, Viniegra-González Gustavo, Augur Christopher
Food Research Department, Faculty of Chemical Sciences, Universidad Autónoma de Coahuila, Unidad Saltillo, México.
Appl Biochem Biotechnol. 2002 Jul-Dec;102-103(1-6):407-14. doi: 10.1385/abab:102-103:1-6:407.
Undesirable protease production by Aspergillus niger Aa-20 in submerged culture and solid-state culture was evaluated using different concentrations of tannic acid as sole carbon source in a model system designed for tannase production. Protease production was found to be dependent on the culture system used (submerged culture or solid-state culture) and on the initial tannic acid concentration. Expression of protease activity in submerged culture was higher (up to 10 times) than activity obtained in solid-state culture, using identical culture medium composition. In submerged culture, the lowest final protease activity (0.13 IU) was obtained with the highest tannic acid concentration, while in solid-state culture protease activity was not affected by changes in initial substrate concentration. Absence of detectable proteolytic activity in solid-state culture is related to high production of tannase enzyme. Hence, the use of solid-state culture for fungal enzyme production may allow for higher and more stable enzyme titers present in culture extracts.
在一个为生产单宁酶而设计的模型系统中,使用不同浓度的单宁酸作为唯一碳源,评估了黑曲霉Aa-20在液体培养和固态培养中产生不良蛋白酶的情况。发现蛋白酶的产生取决于所使用的培养系统(液体培养或固态培养)以及初始单宁酸浓度。在使用相同培养基成分的情况下,液体培养中蛋白酶活性的表达高于固态培养中获得的活性(高达10倍)。在液体培养中,单宁酸浓度最高时最终蛋白酶活性最低(0.13 IU),而在固态培养中,蛋白酶活性不受初始底物浓度变化的影响。固态培养中未检测到蛋白水解活性与单宁酶的高产量有关。因此,使用固态培养生产真菌酶可能会使培养提取物中酶的滴度更高且更稳定。