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First physical plans. I am teaching summer session at the University of Washington from June 19 - - July 19, and plan thereafter
to spend a little time climbing in the Grand Tetons with a couple of friends. However, I should get back to Berkeley during
the first week of August. This program is conditional on my still being a member of the U.C. faculty at that time, which
is by no means certain. I've been well to the front of the battle with the Regents over the loyalty oath issue, and this
political problem had taken a large part of my time during the post academic year. The settlement finally attained is one
of which I deeply disapprove, and I haven't made up my mind whether is accept it and stay or go elsewhere. If the latter,
I'll probably be busy moving at the end of the summer. So I can't promise anything definite at present.
Have you heard from our housing bureau yet? They have your name listed, and should be beginning to some through with rental
possibilities. If you don't receive any information from them during the next couple of weeks let me know, and I'll
see what can be done in the way of direct action (ad. in the local paper).
Are you planning to go to the SAB meetings? I'll be there, and will probably know more clearly by then about my own future.
Second, scientific matters. With reference to your query re. paper II, I suspect that rapidly-dried cells are still in large
measure viable, but we have
never determined this, since our interest at that time was to get cells that would not behave like living ones, and could
thus be used to study the various individual step-reactions. This is something that derives systematic study but hasn't
yet received it. My work has been pretty much at a standstill for the last 7-8 months as a result of heavy teaching and loyalty
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I don't know what to make of your K-12 mutant which forms a constitutive galactosidose ; particularly its substantive
responses seem most prevention. On the other hand, the finding that K-12 on rich media can be "pre-adapted" in the
absence of scientific substitutes doesn't frighten me too much. It could mean that precursors and available energy are
present so abundantly that the adaptive bug is reduced to the point of no longer being experimentally observable. This is
the orthodox explanation, of course. There is naturally the alternative that the enzymes are actually produced in the absence
of the specific substrate. It might be instructive to find out whether the presence of INP has any effect on the rate of attack
when added before the specific substitute. If the former explanation is correct, there might be a detectable rate-difference
over a period of 60 minutes or so between treated and untreated cells. If the latter, there should be none.
Am very busy just now, so will write no more. I hope you'll be in Baltimore so that we can talk over some of these matters.