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A novel recombinant chlorophyllase from cyanobacterium Cyanothece sp. ATCC 51142 for the production of bacteriochlorophyllide a.
Chou, Yi-Li; Lee, Ya-Lin; Yen, Chih-Chung; Chen, Long-Fang O; Lee, Li-Chiun; Shaw, Jei-Fu.
  • Chou YL; Institute of Biotechnology, National Cheng Kung University, Tainan, Taiwan.
  • Lee YL; Institute of Plant and Microbial Biology, Academia Sinica, Taipei, Taiwan.
  • Yen CC; Biotechnology Division, Taiwan Agricultural Research Institute, Taichung, Taiwan.
  • Chen LF; Department of Biological Science and Technology, I-Shou University, Kaohsiung, Taiwan.
  • Lee LC; Institute of Plant and Microbial Biology, Academia Sinica, Taipei, Taiwan.
  • Shaw JF; Department of Nutrition, I-Shou University, Kaohsiung, Taiwan.
Biotechnol Appl Biochem ; 63(3): 371-7, 2016 May.
Article en En | MEDLINE | ID: mdl-25828734
ABSTRACT
Bacteriopheophorbide a (BPheid a) is used as a precursor for bacteriochlorin a (BCA), which can be used for photodynamic therapy in both in vitro and in vivo biochemical applications. This study successfully isolated and expressed a photosynthetic bacterium (Cyanothece sp. ATCC 51142) chlorophyllase called CyanoCLH, which can be used as a biocatalyst for the production of a BCA precursor by degrading bacteriochlorophyll a (BChl a). Substrate specificity and enzyme kinetic analyses were performed and the results verified that the recombinant CyanoCLH preferred hydrolyzing BChl a to produce bacteriochlorophyllide a (BChlide a), which can be converted to BPheid a by removing magnesium ion. The recombinant CyanoCLH was cloned and expressed in Escherichia coli BL-21 (DE3), and its molecular weight was 54.7 kDa. The deduced amino acid sequence of the recombinant CyanoCLH comprised a unique lipase-motif GHSLG, which differs from the GHSRG sequence of other plants and lacks a histidine of the typical and conserved catalytic triad Ser-Asp-His. The recombinant CyanoCLH was subjected to biochemical analyses, and the results indicated that its optimal pH and temperature were 7.0 and 60 °C, respectively.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas Recombinantes / Hidrolasas de Éster Carboxílico / Bacterioclorofila A / Cyanothece Idioma: En Año: 2016 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas Recombinantes / Hidrolasas de Éster Carboxílico / Bacterioclorofila A / Cyanothece Idioma: En Año: 2016 Tipo del documento: Article