Biomedical Engineering Reference
In-Depth Information
Madigan, M.T., Martinko, J.M., Parker, J., 1997. Brock Biology of Microorganisms, 8th ed., Prentice Hall, Upper Saddle
River, NJ.
Moran, L.A., Scrimgeour, K.G., Horton, H.R., Ochs, R.S., Rawn, J.D., 1994. Biochemistry, 2nd ed., Prentice Hall,
Upper Saddle River, NJ.
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Stephanopoulos, G.N., Aristidou, A.A., Nielsen, J., 1998. Metabolic Engineering: Principles and Methodologies.
Academic Press: San Diego, CA.
Vonhippel, P.H., 1998. An Integrated Model of the Transcription Complex in Elongation, Termination and Editing,
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PROBLEMS
10.1. Why is mRNA so unstable in most bacteria (half-life of about 1 min)? In many higher
organisms, mRNA half-lives are much longer (
1 h). Why?
10.2. What would be the consequence of one base deletion at the beginning of the message
for a protein?
10.3. S.B. Lee and J.E. Bailey (“Genetically structured models for lac promoter-operator
function in the E. coli chromosome and in multicopy plasmids: lac promoter function”,
Biotechnology & Bioengineering, 26: 1381 e 1389, 1984) modeled the lac-operon by
including binding of the repressor to a nonspecific binding site in the chromosome (X d ).
Neglecting the binding of inducer to the repressor-operator complex, the equilibria are
given by
>
K 1 E r ð
E r þ m
S L 4
S L Þ m
(P10.3-1)
K 2 E o E r
E O þ
E r 4
(P10.3-2)
S L Þ m K 3 E O E r ð
E O þ
E r ð
S L Þ m
(P10.3-3)
K 4 X d E r
X d þ
E r
(P10.3-4)
4
K 5 X d E r ð
X d þ
E r ð
S L Þ m 4
S L Þ m
(P10.3-5)
(a) assuming [X d ] T z
[X d ], show
S L T ð1 þ K 5 ½X d T Þ
½
E O
1 þ K 4 ½X d T þ K 1 ½
E O T ¼
(P10.3-6)
S L T ð1 þ K 5 ½X d T ÞþK 2 ½
½
1 þ K 4 ½X d T þ K 1 ½
E r T
where K's are equilibrium constants.
(b) Let K 1 ¼
10 7 mol 1 l, K 2 ¼
10 12 mol 1 l, K 3 ¼
10 9 mol 1 l, K 4 ¼
10 3 mol 1 l,
2
2
10 9 mol 1 l, and [X d ] T ¼
10 2 mol/l and [E r ] T ¼
10 8 mol/l. Plot
K 5 ¼
1.5
4
2
the value of the free to total operator ratio (with m
¼
4), both from Eqn (P10.3-6)
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