1
Philip Handler, ed., Biology and the Future of Man, (New York: Oxford
University Press, 1970), p. 187.
2
Ibid., p. 45.
3
Ibid., p. 48.
4
Wernher von Braun, quoted in Associated Press dispatch in The Cleveland Plain Dealer
of July 19, 1969, p. 5.
5
Harold J. Morowitz, Biological Self-Replicating Systems,
Progress in Theoretical Biology, ed. Fred M. Snell (New York: Academic Press, 1967),
Vol. 1, pp. 35 ff.
6
The speed of replication of DNA is inconceivably fast, ranging apparently to 750 or
1,000 nucleotides per second added to each strand for each growing point in some cases.
The duplication process involves a growing point complex consisting of proteins and perhaps
RNA. Several reports indicate the growing point may be closely associated with the
cell membrane. Investigation proceeds at a furious pace, and anything we record is
therefore subject to revision as more knowledge of the process is revealed by research.
Robert E. Bird and co-workers report that bacterial replication generally involves a
bidirectional fork, with movement of the fork in opposite directions simultaneously at the same
velocity. (Origin and Sequence of Chromosome Replication in Escherichia coli,
Journal of Molecular Biology, Vol. 70, 1972, pp. 549, 563.) Roger Y. Stanier, et al.,
describe multiple forks, apparently occurring when two daughter DNA double-helix molecules
begin replicating before the original forks have completed their cyclemaking possible
a cell division time of twenty minutes. (The Microbial World, 3rd ed. [Englewood
Cliffs, N.J.: Prentice-Hall, Inc., 1970], pp. 294 ff., 374 ff.). The circular DNA
molecule in the bacterium Escherichia coli has perhaps five million nucleotide pairs.
Its usual cell division time under good conditions is forty minutes without multiple forks.
If this involves bidirectional movement of the fork, the number of nucleotides added
per strand per fork movement would be just over 1,000, for each of the two
forks moving apart from each other. E. coli can replicate in twenty
minutes, but at this speed, multiple forks may be involved.
John Cairns reported a replication speed requiring 15,000 turns per minute
in unwinding the double helix. (The Bacterial Chromosome, Scientific American,
Vol. 214, [January 1966], p. 42.) For unwinding, it is now thought that
enzymes make nicks in one side of the helix. As the fork moves along, one strand
is polymerized continuously in the same direction as fork movement. The other
strand is apparently formed in the opposite direction in short fragments, later
to be joined into a complete circular daughter molecule. Many mysteries remain
in this amazing process. (This, or some such process, is necessary because
nucleotides join only onto the 3' end of a new forming strand. In the DNA double
helix, the strands are polarized oppositely to each other, with the 5' end of one
strand across from the 3' end of the other.)
7
Morowitz, personal communication, November, 1970.
8
Morowitz, personal communication, November, 1970.
9
Considering the human genome (DNA per cell) as three billion nucleotide pairs averaging
1,200 per gene.
10
Harold J. Morowitz, Energy Flow in Biology (New York: Academic Press,
1968),pp.12ff.
11
Philip Handler, ed., Biology and the Future of Man, p. 168.
12
This figure is based on a ratio of 115/10,000 phosphorus atoms to silicon atoms (ibid.),
and on the radius and mean density used earlier on page 118.
Dr. George Preston, of the California Institute of Technologys Hale Observatories,
has pointed out that one should not now put undue confidence in tables of cosmic abundance.
There are many uncertainties and variables. The universe is not static in this regard.
Elements are constantly being formed from other elements in the interior of stars.
These elements may then be scattered by supernova explosions. A small percentage of
certain classes of stars now indicate unexpected proportions of some elements on their surfaces,
including phosphorus. Interior composition is uncertain.
(George Preston, California Institute of Technology, personal telephone conversation, December, 1971.)
For our purpose, however, the figure used above is reliable enough. Chance will fail
this test by such a margin that it would not matter if the number of phosphorus atoms had to
be changed, regardless of extent.
13
Eight trillion per second in each set! That is 1081 per second for all the sets.
14
Marshall W. Nirenberg, National Institutes of Health, personal telephone
conversation, October, 1971.
15
Philip C. Hanawalt, Stanford University, personal telephone conversation,
November, 1971.
16
Joseph Ilan, The Role of tRNA in Translational Control of Specific mRNA During
Insect Metamorphosis, Symposia on Quantitative Biology (Long Island, N,Y.:
Cold Spring Harbor Laboratory, 1970), pp. 787-791.
17
C. Thomas Caskey, Arthur Beaudet, and Marshall W. Nirenberg, RNA Codons and Protein
Synthesis, Journal of Molecular Biology, Vol. 37 (1968), pp. 99-118.
18
For discussion of substitution limits, see footnote 9 in chapter 6, p. 100.
Substituting one amino acid for another is thought to be usually lethal or
deleterious. Since there are evidently some substitutions that can at least be
tolerated if limited to about one substitution per chain on the average, not in the
active site, we are again figuring it with chance getting the advantage.
19
Warren Weaver, Lady Luck, Theory of Probability (Garden City, New York: Doubleday, 1963), p. 111.
20
Ibid., pp. 235, 236.
21
Irving Adler, Probability and Statistics for Everyman (New York: John Day
Co., 1963), p. 13.
22
It might be mentioned that the probability of at least one usable gene is even less than the
impossibly remote chance we calculated. There is a rule called Poissons formula
which can be used when the number of tries is very large and the probability very small.
If the probability is, on the average, one in a huge number, actually one would have a 37%
probability, rounded, that not even one would occur in that number of trials. There would
also be a 37% chance of exactly one, 18% chance of exactly two occurring, 6% chance of three,
and 1% chance of four, and a small fraction of a percent for five. (Émile Borel,
Probabilities and Life (New York: [Dover Publications, 1962], pp. 73, 74.)
This formula arises from the fact that in any series of tries, you will not always get exactly
the average expected result, but sometimes more, sometimes less. For example, in drawing
from ten numbered coins, the average probability is to get the number one once in ten draws.
If a person does several different series of ten draws each, he will find that in some series
he does not get the number one at all, and in some he obtains it twice or even three times.
If, instead of a 1/10 probability, the number is quite large, like 1 chance in 10,000 or 100,000,
then the expected percent of the series with zero, one, two, and three times can be calculated by
use of Poissons formula. It involves a mathematical symbol, e, which is 2.718....
If the average probability is one in a number like, for example, 105, the chance of
getting none at all in a given series is 1/e, which is 36.788...%. The same formula
tells the chance of getting exactly one. For the chance of getting two or more, the formula
becomes 1/e2! or 1/e3!, etc. (e3! is 2.718 x 3 x 2 x l). We have
checked this out in experiments involving large numbers and it proved true.
With the size of the odds we have found for one gene, even dividing it by five would make little
difference, since it would reduce it less than one zero [i.e., less than one order of magnitude].
23
André de Cayeux, Three Billion Years of Life (New York; Stein and Day,
1969), p. 208.
24
George Wald, The Origin of Life, Scientific American (August, 1954),
p.48.
25
Joseph L. Henson, Bob Jones University, personal correspondence, December, 1971.
26
The ratio of 1/10236 is the probability, and 10147 is the number of
years it would take, as calculated on p. 160.
27
Kenneth K. Landes, Geotimes, Vol. III (March, 1959), p, 19.
28
Dr, Morowitz has described the interesting fact that a degree of order is sometimes produced
by energy flow, (Morowitz, Energy Flow in Biology.) The extent of such naturally
produced order is quite different from the degree of order required for the simplest living
thing. As an example of order from energy flow, we might consider the wind bringing a
degree of order in autumn leaves. The limitations of order produced in this manner are
clearly quite confining, in the absence of intelligent planning, regardless of the amount of
energy flow.
29
Émile Borel, Elements of the Theory of Probability (Englewood Cliffs, N.J.: Prentice-Hall,
Inc., 1965), p. 57.
30
Émile Borel, Probabilities and Life (New York: Dover Publications, 1962), p. 28.
Regarding Borels use of the minus exponent, the reader may recall that this means the
same as writing the number as a fraction with the figure 1 on top. 10-50 is the
same as 1/1050 or 1 chance in a figure with 50 zeroes.
31
Hebrews 1:3 NEB
32
John 7:17 NEB
33
Hebrews 1:2