Isolation and Identification of Agarose-degrading Bacterium, Pseudoalteromonas sp. GNUM08122

This study's aim was to isolate microorganisms producing agarase with a high activity, with possible applications in improving the performance of the pretreatment processes for bioethanol production. Marine algaes were collected from the south coast of Korea, from which three kinds of microorga...

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Published inKorean Journal of Microbiology and Biotechnology Vol. 40; no. 1
Main Authors Kim, Y.N., Gyeongsang National University, Jinju, Republic of Korea, Jeong, Y.K., Gyeongsang National University, Tongyeong, Republic of Korea, Kim, M.C., Gyeongsang National University, Tongyeong, Republic of Korea, Kim, S.B., Gyeongsang National University, Jinju, Republic of Korea, Chang, Y.K., Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea, Chi, W.J., Myongji University, Yongin, Republic of Korea, Hong, S.K., Myongji University, Yongin, Republic of Korea, Kim, C.J., Gyeongsang National University, Jinju, Republic of Korea
Format Journal Article
LanguageKorean
Published 01.03.2012
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Summary:This study's aim was to isolate microorganisms producing agarase with a high activity, with possible applications in improving the performance of the pretreatment processes for bioethanol production. Marine algaes were collected from the south coast of Korea, from which three kinds of microorganisms were isolated. After a 4-day culture of these strains at 25℃, crude enzymes were obtained from culture supernatant or cell-free extract by ammonium sulfate precipitation and membrane dialysis. Agarase activity was observed in these crude enzymes. Notably higher specific activity was observed in the crude enzyme obtained from the culture supernatant rather than that from the cell-free extract. This indicates that a secreted enzyme has a much greater activity than a cellular enzyme. Crude enzymes from the GNUM08122 strain were inferred to have α-agarase activity because release of p-nitrophenol was observed, possibly due to the cleavage of p-nitrophenyl-α-D-galactopyranoside. The 16S rRNA sequence of GNUM08122 showed a close relationship to Pseudoalteromonas issachenkonii KMM 3549 (99.8%) and Pseudoalteromonas tetraodonis IMA 14160 (99.7%), which led us to assign it to the genus Pseudoalteromonas. Biochemical and physiological study revealed that this strain can grow well at 40℃ under a wide range of pH (pH 4~8) in high-salt conditions (10% NaCl).
Bibliography:A50
ISSN:1598-642X
DOI:10.4014/kjmb.1112.12002