I am sorry to hear of the shadow in your prospects at Caltech for next year. Except for industrial or government openings,
there haven't been many opportunities come to light. Are you interested in these? Universities generally have become very
wary of taking on new staff personnel owing to the prospects of dropping enrollments, and this is particularly acute at state
institutions. I suppose that applications are still being taken for some fellowships, notably another round of PHS. I wish
it were possible to invite you to name this department in such an application, but I am afraid that space reallocations and
remodelling are being delayed in a way that leaves us barely able to meet present commitments. However, if you should become
interested in some such arrangement, especially for early 1952 or later, let me know and I'll keep you posted.
Max was here a couple of months ago and mentioned his qualifications to your kinetic work. He particularly mentioned a few
points in your technique which I did not quite understand--viz. shaking suspensions in flasks with a layer of agar. I hope
your paper (in Genetics in Press?) gives enough detail so that we can try to repeat some of the experiments. I still think
that kinetics, by itself, is a waste of time unless used as a direct guide for more tangible experiments. Have you found any
recombination inhibitors in supernatants of old broth cultures? I can't pretend to understand the s-/ story: what's
the difference between liquid and agar? You say that s-/ x s- gives all s-/. How about s- x s- under the same conditions?
By the way, you could have saved some trouble with your K-12 s-/ by using streptomycin-minimal and crossing W1177 (which Dulbecco
has, I think). It's perfectly all right to give out the cultures you mentioned, but I'd like to keep track of who
has them. Who has any use for W-1205! Also, I notice that Ryan "published" Y-9 as 679-680-meth (in MGB). To the best
of my recollection, this does better with pab than meth. But it's a lousy mutant, and its only interest is that it was
the first mutant to be isolated by limiting enrichment. I am interested to hear so much activity with bacteria at Caltech
-- is phage petering out?
Most of my own time is spent on routine picking out of new fertile strains (about a dozen from over three hundred screened),
and in cleaning up (the data, not the interpretation) of heterzygote behaviour. Esther is working on the segregation of lambda,
and similar genetics. Norton Zinder has a couple of Salmonella mutant stocks whaich are perfectly stable, and give very high
yields of prototrophs when mixed, but the unselected so far tested have not shown very many new combinations. Are you coming
east for the SAB meeting in Chicago (on May 30) or OSH (June 8-15)? Lots of jobs are picked up that way.