EVALUATION OF THE EFFECT OF GLUCOSE AND CARBOXYMETHYLCELLULOSE ON THE ENDOGLUCANASE PRODUCTION BY Bacillus spp.

MARTÍNEZ, EZEQUIEL M; GUINDÁN, CAROLOS J; MANFREDI, ADRIANA PAOLA; PEROTTI, NORA INÉS; MARTINEZ, M. ALEJANDRA

Rosario

Congreso; IX Congreso Argentino de la Sociedad de Microbiología General; 2013

SAMIGE (Sociedad de Microbiología General)

The production of bioethanol from the abundant and renewable lignocellulosic biomass has risen as a promising approach in the recent years. Cellulose, the most common natural renewable biopolymer, is degraded by the hydrolytic action of a multicomponent enzyme system which represents the key step for such biomass conversion. This enzymatic hydrolysis requires the synergistic action of exoglucanases, endoglucanases and b-glucosidases. As a whole, cellulases contribute the 8% of the worldwide industrial enzyme demands, which are expected to increase by 100% within 2014. As a source of novel cellulases, Bacteria are considered a valuable source of enzymes due to their high growth rate and their diverse endowment of glycoside hydrolases. Hence, we evaluated a collection of cellulase producing bacteria isolated from guts of phytophagous insects. As a result, two isolates were selected due to their high endoglucanases production. These isolates were named as AR03 and AR408 and taxonomically identified as Bacillus spp. by means of the 16S rRNA gene sequences analysis. A limiting factor in the production of enzymes in our study was the low biomass obtained in mineral media with cellulose as the sole carbon source. Thus, we used a modified peptone broth based on a commercial culture media in order to increase the microbial growth. Then, the media components were evaluated by using a systematic approach through factorial design with the statistical software MINITAB® (14.12.0), in order to assess the most useful conditions for enzyme production. Once achieved a good bacterial growth, we tested glucose and carboxymethylcellulose (CMC), individually and combined, as substrates for the production of endoglucanases. The enzymatic activity was quantified by determining reducing sugars released with the 3,5-Dinitrosalicylic acid (DNS) reagent. Despite the fact that the two isolates studied were closely related as Bacillus species, they displayed a different behavior. AR03 produced the highest enzymatic activity using CMC (1.15 U/mL), but also showed a significant ability to produce endoglucanases using media with glucose and in the absence of CMC, reaching activities over 0.50 U/mL. On the other hand, AR408 produced endoglucanases only in the presence of CMC in the culture medium.