L-lysine α-oxidase
(LO) is one of a few microbial enzymes with therapeutic potential in certain
cancers. The enzyme has been determined in several bacteria and fungi. Its
production is mainly regulated by carbon sources and oxygen. . Thus, the aim of
this study was to determine the nutritional requirements and effect of oxygen
concentration on the production of LO in P. aeruginosa, and in their
recombinants using a highly efficient oxygen uptake system, the Vitreoscilla
hemoglobin. This study concerns the effect of a higher oxygen uptake provided
by a recombinant system, the Vitreoscilla
hemoglobin, on the production of LO in Pseudomonas
aeruginosa. The results showed that
the recombinant bacterium expressing Vitreoscilla
hemoglobin gene (vgb) had distinct
L-lysine activity from the host strain under both carbon catabolite repression
and no repression conditions. In a rich medium supplemented with glucose, the
recombinant strain showed 20-40 % higher L-lysine activity than the host
strain. This difference was even more significant in the medium with no glucose
supplement, where the recombinant strain showed almost 2-fold higher enzyme
activity throughout the incubation. The results sometime were contradictory in
terms of the effect of carbon source (mainly glucose) and oxygen on the
production of this enzyme.
| Primary Language | English |
|---|---|
| Journal Section | Research Article |
| Authors | |
| Submission Date | March 8, 2018 |
| Publication Date | September 19, 2018 |
| Published in Issue | Year 2018 Volume: 13 Issue: 2 |