Thesis-PDF - IAP/TU Wien
Thesis-PDF - IAP/TU Wien
Thesis-PDF - IAP/TU Wien
You also want an ePaper? Increase the reach of your titles
YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.
Chapter 7<br />
Outlook<br />
The Atomic Force Microscope (AFM) has proven to be a valuable tool for investigation<br />
of biomaterials at the small scale. In this work the single celled alga Euglena<br />
gracilis was investigated in the light of being a bionanotechnological system accommodating<br />
a wealth of functional units within only small volume. A method<br />
for AFM data acquisition of the alga Euglena gracilis was developed and further<br />
investigation can build upon this approach.<br />
As this work is only a beginning of the AFM study of this alga, it focused on its<br />
morphology, on how to obtain first image data of Euglena’s pellicle and some of its<br />
functional cell organelles with potential for technical applications. This undertaking<br />
can be seen as an ignition part in the investigation of algal materials exhibiting<br />
molecular precision achitecture and complexity inherent to living systems.<br />
While the data obtained on whole cells as well as cell organelles provided<br />
essentially morphological data and proved the feasibility of such studies by means<br />
of AFM, other analytical characterization methods, e.g AFM force spectroscopy,<br />
are now possible on these and similar algae by making use of the preparation<br />
method developed herein. Since AFM yields information about the sample as well<br />
as it allows manipulation on the micro and nanoscale, future research attempts<br />
along these lines seem encouraging.<br />
The exact nature of the novel features found, i.e. the indentations in the<br />
center of pellicular strips, should be further analyzed, especially with regards to the<br />
sample preparation techniques used. Equally interesting, AFM force spectroscopy<br />
shall characterize the mucus material ejected by mucus excretion pellicle pores.<br />
Further, elucidation about the three-dimensional structure of the photoreceptor<br />
was attempted with this work, however, the fraction of crystalline parts<br />
contained too few photoreceptors to be found with the AFM tip, since crystalloid<br />
bodies, paramylon grains and not completely removed cell material amounted for a<br />
large portion of the fraction. Possible future approaches comprise the development<br />
of a preparation technique for a solution containing a plentitude of photoreceptors.<br />
92