首页> 外文会议>International Conference on Food Science and Engineering >Polygalacturonase production by AR2 pectinolytic bacteria through submerged fermentation of raja nangka banana peel {Musa paradisiaca var. formatypica) with variation of carbon source and pectin
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Polygalacturonase production by AR2 pectinolytic bacteria through submerged fermentation of raja nangka banana peel {Musa paradisiaca var. formatypica) with variation of carbon source and pectin

机译:通过Raja Nangka Banana Peel的淹没发酵来通过淹没发酵来产生PolyGalactulonase通过Raja Nangka Banana Peel {Musa Paradisiaca var。 Formarypica)具有碳源和果胶的变异

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Polygalacturonase (EC 3.1.2.15) catalyzes the hydrolysis of a-l,4-glycosidic bonds on galacturonic acid. Polygalacturonase can be produced from AR2 pectinolytic bacteria isolated from orange peel and vegetable waste. Commonly cost production of enzymes were high. However, with the advancement of technology, enzymes can now be manufactured at a low cost. Production of enzymes in low cost media with agro-industrial waste is interesting. Raja nangka banana peel is agro-industrial waste that is uneconomic. Therefore, this material can be used as a pectin source in polygalacturonase production. Polygalacturonase was produced by AR2 pectinolytic bacteria with the addition of various carbon sources (1 % glucose, 1 % galactose, 1 % lactose) and variation of pectin concentrations (5%; 7.5%; 10%). This study used submerged fermentation with a cultivation temperature of 55°C and an agitation speed of 144 rpm for a 48-h incubation time. The results showed that variation of carbon sources and pectin concentrations affected the production of polygalacturonase. After 48 h fermentation, the results showed that the number of cells of samples ranged from 8.3 to 9.445 log cells/mL; the used pectin of samples ranged from 87.170-93.745%; and the polygalacturonase activity of samples ranged from 0.030 to 0.151 U/mL. The highest polygalacturonase activity was obtained by production of polygalacturonase on 1% glucose and 10% pectin medium.
机译:polygalactulonase(EC 3.1.2.15)催化在半乳糖醛酸上的A-L,4-糖苷键的水解。聚半乳糖酸盐酶可以由橙皮和蔬菜废物分离的Ar2果胶溶液产生。酶的常见产量高。然而,随着技术进步,现在可以以低成本制造酶。具有农业工业废物的低成本媒体的酶生产是有趣的。 Raja Nangka Banana Peel是农业工业废物,不经济。因此,该材料可用作多肢乳突酶生产中的果胶源。通过AR2果胶溶解细菌产生多肢乳糖酶,并加入各种碳源(1%葡萄糖,1%半乳糖,1%乳糖)和果胶浓度的变异(5%; 7.5%; 10%)。该研究使用培养温度55℃的浸没式发酵和144rpm的搅拌速度为48小时孵育时间。结果表明,碳源和果胶浓度的变异影响了多甲醛酶的产生。 48小时发酵后,结果表明,样品的细胞数量范围为8.3至9.445个对数/ mL;样品的二手果胶范围为87.170-93.745%;样品的多糖尿酸酶活性范围为0.030至0.151 u / ml。通过在1%葡萄糖和10%果胶培养基上产生多戊酰脲酶来获得最高的多糖尿酸酶活性。

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