الفهرس 
introduction
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Abstract
To sum up, this study was done on the two genes ribC and parN.
ribC was heterologously expressed in E. coli and produced functional 2-
deoxy-scyllo-inosose synthase. Thus, the function of the gene was
verified. Also, the produced enzyme can be used to convert glucose-6-
phosphate into 2-deoxy-scyllo-inosose (DOI) which is an important
compound. 001 can be easily converted into valuable benzenoid
compounds such as catechol and hydroquinone, or into cyclitols used for
drug synthesis, by simple chemical reactions.
The present work shows the possibility of heterologous
production of functional 2-deoxy-scyllo-inosose from Streptomyces
ribosidificus in E. coli.
ribC and parN were successfully cloned into the shuttle vector
pUWL20 I PW creating the recombinant plasmids pUWRC and pUWPN,
respectively. The gene ribC was transformed into S. ribosidificus, i.e. the
gene was duplicated.
Chapter VI
VI. Summary & Conclusion