Abstract
DNA
crown cells (artificial cells), in which the outside of the membrane is covered
with DNA, can be readily synthesized in vitro using sphingosine
(Sph)-DNA-adenosine mixtures to produce synthetic DNA crown cells. As these DNA
crown cells can proliferate within egg whites, many kinds of synthetic DNA
crown cells and DNA crown cells can be prepared using DNA from a variety of
donors. Though the methods for synthesis are well established, how synthetic
DNA crown cells are able to proliferate in egg whites remain unclear. Previous
studies have demonstrated that assemblies of synthetic DNA (E. coli) crown
cells were formed in response to the inorganic substances contained in egg
white, and that modified synthetic DNA crown cells were produced within such
assemblies. Moreover, the cells in these assemblies were not released after the
addition of monolaurin. Rather, the assembly formed crystal-like substances and
the cells disappeared. In the present study, it was examined whether cells were
regenerated with two monolaurin treatments. Here, it was described that cells
were produced from the assembly of synthetic DNA (E. coli) crown cells which
form crystal-like substances with stimulation by monolaurin twice. The cell
proliferation experiments were carried out as follows:
a)
Synthetic DNA (E. coli) crown cells were incubated for 18 hours at 37℃ and these cells formed
assemblies.
b)Monolaurin
was added to the assemblies and the mixtures were incubated for 36 hours at 37℃.
c)
The assemblies then transformed into crystal-like substances.
d)Monolaurin
was added to these reconstructed synthetic DNA (E. coli) crown cells and the
mixtures were incubated for 20–40 minutes at 37℃, which
is when cell proliferation was observed.
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