Genetic Approach for the Fast Discovery of Phenazine Producing Bacteria
نویسندگان
چکیده
A fast and efficient approach was established to identify bacteria possessing the potential to biosynthesize phenazines, which are of special interest regarding their antimicrobial activities. Sequences of phzE genes, which are part of the phenazine biosynthetic pathway, were used to design one universal primer system and to analyze the ability of bacteria to produce phenazine. Diverse bacteria from different marine habitats and belonging to six major phylogenetic lines were investigated. Bacteria exhibiting phzE gene fragments affiliated to Firmicutes, Alpha- and Gammaproteobacteria, and Actinobacteria. Thus, these are the first primers for amplifying gene fragments from Firmicutes and Alphaproteobacteria. The genetic potential for phenazine production was shown for four type strains belonging to the genera Streptomyces and Pseudomonas as well as for 13 environmental isolates from marine habitats. For the first time, the genetic ability of phenazine biosynthesis was verified by analyzing the metabolite pattern of all PCR-positive strains via HPLC-UV/MS. Phenazine production was demonstrated for the type strains known to produce endophenazines, 2-hydroxy-phenazine, phenazine-1-carboxylic acid, phenazine-1,6-dicarboxylic acid, and chlororaphin as well as for members of marine Actinobacteria. Interestingly, a number of unidentified phenazines possibly represent new phenazine structures.
منابع مشابه
The forgotten role of methenamine to prevent recurrent urinary tract infection: urgency for reuse 100 years after discovery
In conclusion, UTI is a globally distributed disease with emergence of multidrug-resistant bacteria; thus, new drug discovery or activation of previously used drugs is an urgent issue. Methenamine has been suggested as a beneficial agent for the UTI prevention as it works as a urinary antiseptic by safely producing formaldehyde to prevent bacterial growth while avoiding bacterial resistance...
متن کاملScreening of Alginate Lyase-Producing Bacteria and Optimization of Media Compositions for Extracellular Alginate Lyase Production
Background: Alginate is a linear polysaccharide consisting of guluronate (polyG) and mannuronate (polyM) subunits. Methods: In the initial screening of alginate-degrading bacteria from soil, 10 isolates were able to grow on minimal medium containing alginate. The optimization of cell growth and alginate lyase (algL) production was carried out by the addition of 0.8% alginate and 0.2-0.3 M NaCl ...
متن کاملThe Introduction of a Heuristic Mutation Operator to Strengthen the Discovery Component of XCS
The extended classifier systems (XCS) by producing a set of rules is (classifier) trying to solve learning problems as online. XCS is a rather complex combination of genetic algorithm and reinforcement learning that using genetic algorithm tries to discover the encouraging rules and value them by reinforcement learning. Among the important factors in the performance of XCS is the possibility to...
متن کاملThe Introduction of a Heuristic Mutation Operator to Strengthen the Discovery Component of XCS
The extended classifier systems (XCS) by producing a set of rules is (classifier) trying to solve learning problems as online. XCS is a rather complex combination of genetic algorithm and reinforcement learning that using genetic algorithm tries to discover the encouraging rules and value them by reinforcement learning. Among the important factors in the performance of XCS is the possibility to...
متن کاملIsolation and molecular identification of bacteria producing alkaline phosphatase enzyme from environmental sources
Alkaline phosphatase (ortho phosphate, monoester hydrolase phosphoinositide E. C. 3.1.3.1) is a non-specific metalloproteinase enzyme that is located inside periplasmic space of bacteria. This enzyme is used to measure freshwater sediment in genetic engineering for cleaning water. Isolation and molecular identification of the bacteria producing alkaline phosphatase and comparison of its product...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره 9 شماره
صفحات -
تاریخ انتشار 2011