Sugar beet is a suitable source for cellulases-producing bacteria and actinomycetes

F. Fahmy, A. Zohri, G. Mohamed, E. Hafez
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Abstract

Introduction Sugar beet is considered the second source of sugar production in the world, but ‎it becomes the first source in Egypt and several other countries all over the ‎world. The present study aimed to convert the agro-industrial beet pulp that ‎consists of cellulosic material into fermentable sugars as a friendly source of ‎energy. The cellulases producing bacteria and actinomycetes are associated with ‎beets' pulps and roots. The study also aimed to optimize the conditions of ‎cellulases production, e.g., incubation time, temperature and pH. One hundred ‎and two isolates of bacteria and actinomycetes were isolated from these samples ‎and then screened to determine their potency to produce cellulases. Seven isolates ‎were recorded as high producers (two from rhizospheres, one from endophytes, ‎and four from the beet pulp). These seven isolates were classified according to ‎morphological and biochemical tests as S11 (Streptomyces), S31 (Streptomyces), ‎S45 (Bacillus), and S72 (Bacillus), S73 (Streptomyces), S85 (Streptococcus) and ‎S88 (Bacillus). Optimization for the incubation period, temperature, and pH ‎showed that activities of the highest three tested isolates S11, S45, and S88 were ‎0.73, 0.17, and 0.54 U/ml after two days of the incubation period. These levels ‎increased to 1.33, 0.24 and 0.76 U/ml on the fourth incubation day at different ‎temperatures and pH degrees. According to the results, it is recommended to use ‎bacteria (Streptomyces), which is sample No. S11 isolated from the rhizosphere ‎soil of beetroots was the high producer of cellulases at 50°C and pH 7.‎
甜菜是生产纤维素酶的细菌和放线菌的合适来源
甜菜被认为是世界上糖生产的第二来源,但它成为埃及和世界上其他几个国家的第一来源。本研究旨在将由纤维素物质组成的农用工业甜菜果肉转化为可发酵糖,作为一种友好的能量来源。产生细菌和放线菌的纤维素酶与甜菜的果肉和根有关。本研究还旨在优化纤维素酶的生产条件,如培养时间、温度和ph。从这些样品中分离出100株和2株细菌和放线菌,并对其进行筛选,以确定其生产纤维素酶的效力。7株菌株被记录为高产菌株(2株来自根际,1株来自内生菌,4株来自甜菜果肉)。经形态学和生化鉴定,7株分离菌株分别为S11(链霉菌)、S31(链霉菌)、S45(芽孢杆菌)和S72(芽孢杆菌)、S73(链霉菌)、S85(链球菌)和S88(芽孢杆菌)。结果表明,菌株S11、S45和S88在培养2 d后活性最高,分别为0.73、0.17和0.54 U/ml。在不同温度和pH值条件下,培养第4天,这些水平分别增加到1.33、0.24和0.76 U/ml。根据实验结果,建议采用链霉菌(Streptomyces)为样品编号。从甜菜根根际土壤中分离得到的S11在50°C和pH为7时高产纤维素酶
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