首页 | 本学科首页   官方微博 | 高级检索  
   检索      


Mutagenic analysis of putative domain II and surface residues in mosquitocidal Bacillus thuringiensis Cry19Aa toxin
Authors:Jong Yul Roh  Manoj S Nair  Xinyan Sylvia Liu  & Donald H Dean
Institution:Institute of Microbiology, Technische Universität Braunschweig, Braunschweig, Germany;;Helmholtz-Centre for Infection Research, Division of Structural Biology, Braunschweig, Germany;and;Helmholtz-Centre for Infection Research, Division of Microbiology, Braunschweig, Germany
Abstract:The growing resistance against antibiotics demands the search for alternative treatment strategies. Photodynamic therapy is a promising candidate. The natural intermediate of chlorophyll biosynthesis, protochlorophyllide, was produced, purified and tested as a novel photosensitizer for the inactivation of five model organisms including Staphylococcus aureus, Listeria monocytogenes and Yersinia pseudotuberculosis , all responsible for serious clinical infections. When microorganisms were exposed to white light from a tungsten filament lamp (0.1 mW cm−2), Gram-positive S. aureus, L. monocytogenes and Bacillus subtilis were photochemically inactivated at concentrations of 0.5 mg L−1 protochlorophyllide. Transmission electron microscopy revealed a disordered septum formation during cell division and the partial loss of the cytoplasmic cell contents. Gram-negative Y. pseudotuberculosis and Escherichia coli were found to be insensitive to protochlorophyllide treatment due to the permeability barrier of the outer membrane. However, the two bacteria were rendered susceptible to eradication by protochlorophyllide (10 mg L−1) upon addition of polymyxin B nonapeptide at 50 and 20 mg L−1, respectively. The release of DNA and a detrimental rearrangement of the cytoplasm were observed.
Keywords:photodynamic therapy  protochlorophyllide              Staphylococcus aureus                        Yersinia pseudotuberculosis                        Listeria monocytogenes
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号