Screening and molecular identification of hypercellulase and xylanase-producing microorganisms for bioethanol production

uThe present study projects the baseline work for bioconversion of pine needles to second generation biofuel, which deals mainly with screening, molecular identification and optimization of process parameters for cellulase and xylanase production. In total, 89 hydrolytic enzymes producing isolates were isolated from the soils and ten potential enzyme producers (seven for cellulase and three for xylanase) were subjected to secondary screening by inducing physical and chemical mutation. The wild and mutant strains of hypercellulase producers N-12 and Kd(1) were identified as Bacillus stratosphericus N-12 and Bacillus altitudinis Kd(1) using 16S rRNA technique. The fungal isolates RF1 and F2 were identified on the basis of 5.8 rRNA ITS technique and identified as Rhizopus oryzae, RF1 and Rhizopus delemar, F2 respectively. The mutant strains B. stratosphericus N-12 (M) and B. altitudinis Kd(1) (M) are highly stable till 10 generations. Cellulase activity increased from 3.230 to 5.983 IU, i.e. 85.23% increase in cellulase activity was achieved. Xylanase production increased from 51.32 to 95.25 IU with 85.60% increase in production. Solid-state fermentation was also performed by potential fungal strains, i.e. R. delemar F2 and R. oryzae RF1 using pine needles as the substrate.

Automated summary

The study focused on screening, molecular identification, and optimization of process parameters for cellulase and xylanase production from pine needles. Mutant strains with increased enzyme production were identified and used for solid-state fermentation, showing promising results in biofuel production.