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Characterization of Cellulose-Degrading Bacteria Isolated from Soil and the Optimization of Their Culture Conditions for Cellulase Production. | LitMetric

AI Article Synopsis

  • Researchers isolated six cellulose-degrading bacteria from soil samples at Kingfisher Lake and the University of Manitoba, identified as different species including Paenarthrobacter sp. and Bacillus sp.
  • The cellulase production of these bacteria was optimized by adjusting environmental conditions like pH, temperature, and substrate concentration, resulting in significant enzyme activity.
  • Sucrose was found to greatly enhance cellulase activity, supporting the potential use of these bacteria as biocatalysts for converting cellulose into glucose in industrial applications.

Article Abstract

The characterization of bacteria with hydrolytic potential significantly contributes to the industries. Six cellulose-degrading bacteria were isolated from mixture soil samples collected at Kingfisher Lake and the University of Manitoba campus by Congo red method using carboxymethyl cellulose agar medium and identified as Paenarthrobacter sp. MKAL1, Hymenobacter sp. MKAL2, Mycobacterium sp. MKAL3, Stenotrophomonas sp. MKAL4, Chryseobacterium sp. MKAL5, and Bacillus sp. MKAL6. Their cellulase production was optimized by controlling different environmental and nutritional factors such as pH, temperature, incubation period, substrate concentration, nitrogen, and carbon sources using the dinitrosalicylic acid and response surface methods. Except for Paenarthrobacter sp. MKAL1, all strains are motile. Only Bacillus sp. MKAL6 was non-salt-tolerant and showed gelatinase activity. Sucrose enhanced higher cellulase activity of 78.87 ± 4.71 to 190.30 ± 6.42 U/mL in these strains at their optimum pH (5-6) and temperature (35-40 °C). The molecular weights of these cellulases were about 25 kDa. These bacterial strains could be promising biocatalysts for converting cellulose into glucose for industrial purposes.

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Source
http://dx.doi.org/10.1007/s12010-022-04002-7DOI Listing

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