Abstract

Thermophilic microorganisms and their enzymes have been utilized in various industrial applications. In this work, we isolated and characterized thermophilic anaerobic bacteria with the cellulose and hemicellulose degrading activities from a tropical dry deciduous forest in northern Thailand. Out of 502 isolated thermophilic anaerobic soil bacteria, 6 isolates, identified as Thermoanaerobacterium sp., displayed an ability to utilize a wide range of oligosaccharides and lignocellulosic substrates. The isolates exhibited significant cellulase and xylanase activities at high temperature (65°C). Among all isolates, Thermoanaerobacterium sp. strain R63 exhibited remarkable hydrolytic properties with the highest cellulase and xylanase activities at 1.15 U/mg and 6.17 U/mg, respectively. Extracellular extract of Thermoanaerobacterium sp. strain R63 was thermostable with an optimal temperature at 65°C and could exhibit enzymatic activities on pH range 5.0–9.0. Our findings suggest promising applications of these thermoanaerobic bacteria and their potent enzymes for industrial purposes.

Highlights

  • Tropical dry deciduous forest could provide a library of thermophilic microorganisms that could be a great reservoir of thermostable enzymes of industrial significance

  • A total number of 502 thermophilic anaerobic bacteria were obtained from soil samples collected from three different sites of tropical dry deciduous forest in Nan province

  • Thermophilic cellulose and hemicellulose degrading bacterium from tropical forest soil isolates in this study except for R53, exhibited significant cellulase activity that could improve biomass degradation efficiency through a biological process

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Summary

Introduction

Novel thermophilic enzymes were screened from rare environmental conditions of the tropical dry deciduous forest in Thailand for their cellulose and hemicellulose degrading abilities. Thermophilic cellulose and hemicellulose degrading bacterium from tropical forest soil between the halo zone and the bacterial colony diameter. Bacterial isolates were enriched in T6 medium supplemented with 1% glucose for 24 h.

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