I would like to congratulate you on your paper, the subject matter of which, and the discussion, I thought excellent. You
have obviously done much more work than I have. I don't know whether this is due to your greater inate [sic] energy or
to your having technical assistance! Reading your paper made me realize the deficiencies in my own and led me to think that
perhaps I have been rather unwise to attempt to theorize at this early stage. Actually I have now cut out all my phage analogies
which Wollman tells me are unsound. As regards your paper, I thought most of the editorial and referees' criticisms fair
and valid. I think that it would have been impossible for the general reader to read and understand without a great deal
of effort. I have now finished revising it and think I have done it with some success. All I have actually done is to classify
parts of it under headings where I thought [ . . . ] helped, altered the construction of a considerable number of long sentences,
added a few explanations where I thought the technological description was too difficult for the uninitiated reader and changed
a few rather "unenglish" phrases. I hope you will not mind my taking these liberties with your paper but in fact
I think you will find it in no way radically altered. I have typed it with triple spacing so that you can re-alter it as
you wish. I will send it to the editor for approval and will bring it to Italy with me, together with the annotated original.
It is hardly worth sending it by post at this stage. You must not thank me. I enjoyed doing
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it because it made me read and absorb your views much more closely and deeply that I would otherwise have done. About Table
2. The trouble here is that the reader has to remember what A means and B means, in addition to 1, 2, 3, 4, 5, 6, (in terms
of TLB,, F + LGMXA) before he can start to appreciate the significance of the actual data. It would help a lot if the six
columns could be headed with particulars of the actual math, thus:
No. of prototrophs showing various arrangements of Lac, Gal, Mal, Xyl, Ara markers from crosses:
Key at bottom, thus -- L = Lactose
G = Galactose
X = Xylose ec.
+ = sugar fermented.
- = absence of fermentation.
And is there any need to have the LGMXA patterns arranged to read head-to-tail for column 4, 5, 6? It seems to me much simpler
to read right across all seven columns. This makes comparison easy without affecting any of the information presented. You
may have some special point to make by the "head-to-tail" system, but I don't see it.
I feel that the major criticism which can be made against my own work -- a very valid one -- is that it has been mainly concerned
with only two strains. But unless one is in the fortunate position of being able to hand out various aspects of the problem
to students, as I gather Lederberg can (not to speak of his wife!), it is a nice point whether to make as much progress as
possible with one system or to consolidate your position in depth as you go along, which may prove tedious and slow. I have
done only one significant
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experiment recently but it may interest you to hear of it now as I prepare to mention it at Palloza[?]. I reasoned that if
the futility of F+ x F+ crosses is due to the occurrence of F- cells (? F-phenocopies or simply due to temporary loss of F)
in F+ clones, individual F+ x F+ contacts actually being sterile, item[?] treatment of an F+ suspension with G[?]M should
render it pure F+, so that F+/smt x F+ crosses should behave like F+ x F- crosses so far as segregation phenomena are concerned.
Here is the result of an experiment.
No. of prototrophs having phenotype:
I regard this as valid evidence which, when taken in conjunction with the somewhat similar but less dramatic effect of UV
on either parent in F+ x F+ crosses (about which I wrote you via J.L.), becomes good evidence.
Oh! one other thing. I have been very interested in your F- phenocopy story but haven't tried to confirm it in curated[?]
cultures yet. However I did find that when I [ . . . ] well washed 24 hr. agar cultures of 58/F+ and W/F- the prototroph
count was about 100 times less than with young brash[?] cultures. I thought this might be due to your F- phenocopy and it
turns out to be
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so. I crossed a washed 24 hr. agar suspension of 58/F+ with a washed young broth[?] culture of W/F- and of W/F+. The rates
for both crosses were low but that with W/F+ was about twice as great as with W/F-. Testing the markers of prototrophs showed
that with W/F+, 58 had behaved almost unchangingly on F-, but the prototrophs developing with W/F-, and their markers, showed
that 58 still had a good deal of F+ activity. This F- phenocopy is a very peculiar business.