July 13, 1951. Dear Stan: I hope the new set of 58-161 and W1177 arrived ok. If you've still kept them, I wonder if you would be willing to send me some sete of your Aerobacter mtants that you said were not crossable, Norton Zinder has gotten some leads on the mechanism of recombination in Salmonella that I'd like to follow up in other related groups of bacteria, and your mterial would save some time. If you'd rather hold on to it to follow it up yourself, just say go: it'll be perfectly all right with me. What I should like to have where possible is a wild type strain plus two non-overlapping double mitants from it. I have the impression that you have made up such seta in a number of distinct strains. Do you remember the problem you started to work out in the lab here~ making mitants in other coli strains for cross teste’? By crossing "-]177 with wild types on minimal streptomycin agar (S$ T-L- x 8° T+L+, selecting for S° T+L+) we have been able to save most of the work, and have isolated about 25 new strains (out of 750 tests) $hag will oroas with K-12, They seem to be of all different antigenic types, and there is no obvious pattern so far with which to recognize a cross-fertile strain without testing it directly. I'm hoping to have a postdoctoral fealow come in and do the iamnogenetiés. If you haven'’ heard about it already, and are still working on isolating mutants of other genetic work, we've developed a new technique that saves a tremendous amount of work for some needs. It involves using sterilized velvet or velveteen dises to print bacterial colonies from one plate to an unlimited series of others. The velvets are mounted on a wooden cylinder, nap up, with the help of q circular hoop. Then, a plateful of colonies is brought down on the velvet, transferring them to its flat surface. This can then be used to print a series of other plates (EMB different sugars} complete and minimal medium; et@.) One general applic tion has been to show that phage- (and, we hope also drug-) resistant mitants occur in preexisting clones in films of bacterial growth on agar plates. Transferring the films to successive phage-coated plates results in a large portion of congruent resistants, which can only mean that resistant clones had been theref to begin with. This may help to @lear up that vexatious problem of ixkwmml directed ys. selected mittations to resistance, in words of few syllables. I have Always had trouble teaching this, especially to students who have had quite some bacteriology before. Sincerely, Joshua Lederberg