Biomedical Engineering Reference
In-Depth Information
2.16.
Contrast the advantages and disadvantages of chemically defined and complex media.
2.17.
You are asked to develop a medium for production of an antibiotic. The antibiotic is to
be made in large amounts (ten 100,000 L fermenters) and is relatively inexpensive. The
host cell is a soil isolate of a fungal species, and the nutritional requirements for rapid
growth are uncertain. Will you try to develop a defined or complex medium? Why?
2.18.
You wish to produce a high-value protein using recombinant DNA technology. Would
you try to develop a chemical-defined medium or a complex medium? Why?
2.19.
Explain what semiconservative replication means.
2.20.
Give characteristic dimensions for each of these cells: E. coli, yeast (S. cerevisiae), liver
cell (hepatocyte), plant cell.
2.21.
What are the differences in the cell envelope structure between gram-negative and
gram-positive bacteria? These differences become important if you wish to genetically
engineer bacteria to excrete proteins into the extracellular fluid.
2.22.
True or False:
a.
An organism that can grow using oxygen as an electron acceptor and can also grow
and metabolize in the absence of oxygen is called facultative.
b.
Yeasts are prokaryotes.
c.
A bacteriophage is a virus that infects bacteria.
d.
When you supplement growth media with amino acids, you should use the
D
-form.
2.23.
Summarize the argument that all chemical energy sources are derived from solar
energy. What is a reasonable definition of renewable and nonrenewable energy
sources?
2.24.
What is the difference between cellulose and hemicelluloses? What are the similarities
and differences between starch, cellulose and fructan?
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