A novel bifunctional endo-/exo-type cellulase from an anaerobic ruminal bacterium |
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Authors: | Kyong-Cheol Ko Yunjon Han Jong Hyun Choi Geun-Joong Kim Seung-Goo Lee Jae Jun Song |
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Affiliation: | (1) Microbe-based Fusion Technology Research Center, KRIBB, 1404 Sinjeong-dong, Jeongeup, Jeonbuk, 580-185, Republic of Korea;(2) Department of Biological Sciences, College of Natural Sciences, Chonnam National University, 300 Yong-Bong Dong, Buk-Gu, Gwangju, 500-757, Republic of Korea;(3) Industrial Biotechnology and Bioenergy Research Center, KRIBB, Daejeon, 305-806, Republic of Korea; |
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Abstract: | An anaerobic microorganism termed AN-C16-KBRB was isolated from the bovine rumen and demonstrated cellulolytic activity on a NB agar plate containing azo-carboxymethyl cellulose. The 16S rRNA gene of the strain was 98% similar to that of Clostridiaceae bacterium SK082 (AB298754) as the highest homology. A novel celEdx16 gene encoding a bifunctional endo-/exocellulase (CelEdx16) was cloned by the shotgun method from AN-C16-KBRB, and the enzyme was characterized. The celEdx16 gene had an open reading frame of 1,104-base pairs, which encoded 367 amino acids to yield a protein of molecular mass 40.4 kDa. The amino acid sequence was 53% identical to that of an endoglucanase from Clostridium thermocellum. CelEdx16 was overexpressed in Escherichia coli and purified using Ni-NTA affinity chromatography. The specific endocellulase and exocellulase activities of CelEdx16 were 15.9 and 3.6 × 10−2 U mg−1, respectively. The Michaelis–Menten constant (K m values) and the maximal reaction velocities (V max values) of CelEdx16 were 47.1 μM and 9.6 × 10−3 μmole min−1 when endocellulase activity was measured and 106.3 μM and 2.1 × 10−5 μmole min−1 when exocellulase activity was assessed. CelEdx16 was optimally active at pH 5.0 and 40°C. |
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