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NOTE] Detection of a Unique Fibrinolytic Enzyme in Aeromonas sp. JH1
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Research Support, Non-U.S. Gov't
NOTE] Detection of a Unique Fibrinolytic Enzyme in Aeromonas sp. JH1
Han-Young Cho 1, Min Jeong Seo 2,3,4, Jeong Uck Park 4, Byoung Won Kang 4, Gi-Young Kim 5, Woo Hong Joo 6, Young-Choon Lee 2,3,4, Yong Kee Jeong 2,3,4
Journal of Microbiology 2011;49(6):1018-1021
DOI: https://doi.org/10.1007/s12275-011-1376-7
Published online: December 28, 2011
1Industrial Bio-materials Research Center, Korea Research Institute of Bioscience and Biotechnology, Yusung, Daejeon 305-600, Republic of Korea, 2Department of Biotechnology, Dong-A University, Busan 604-714, Republic of Korea, 3Department of Medical Bioscience, Dong-A University, Busan 604-714, Republic of Korea, 4Medi-Farm Industrialization Research Center, Dong-A University, Busan 604-714, Republic of Korea, 5Laboratory of Immunobiology, Department of Marine Life Sciences, Jeju National University, Jeju 690-756, Republic of Korea, 6Department of Biology, Changwon National University, Kyungnam 641-713, Republic of Korea1Industrial Bio-materials Research Center, Korea Research Institute of Bioscience and Biotechnology, Yusung, Daejeon 305-600, Republic of Korea, 2Department of Biotechnology, Dong-A University, Busan 604-714, Republic of Korea, 3Department of Medical Bioscience, Dong-A University, Busan 604-714, Republic of Korea, 4Medi-Farm Industrialization Research Center, Dong-A University, Busan 604-714, Republic of Korea, 5Laboratory of Immunobiology, Department of Marine Life Sciences, Jeju National University, Jeju 690-756, Republic of Korea, 6Department of Biology, Changwon National University, Kyungnam 641-713, Republic of Korea
Corresponding author:  Yong Kee Jeong , Tel: +82-51-200-7557, 
Received: 1 August 2011   • Accepted: 2 November 2011
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A fibrinolytic enzyme was found in a Gram-negative bacterium, Aeromonas sp. JH1. SDS-PAGE and fibrinzymography showed that it was a 36 kDa, monomeric protein. Of note, the enzyme was highly specific for fibrinogen molecules and the hydrolysis rate of fibrinogen subunits was highest for α, β, and γ chains in that order. The first 15 amino acids of N-terminal sequence were X-D-A-T-G-P-G-G-N-V-X-T-G-K-Y, which was distinguishable from other fibrinolytic enzymes. The optimum pH and temperature of the enzyme were approximately 8.0 and 40°C, respectively. Therefore, these results provide a fibrinolytic enzyme with potent thrombolytic activity from the Aeromonas genus.

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    NOTE] Detection of a Unique Fibrinolytic Enzyme in Aeromonas sp. JH1
    J. Microbiol. 2011;49(6):1018-1021.   Published online December 28, 2011
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