Rollin Hotchkiss

Rollin Douglas Hotchkiss (September 8, 1911 – December 12, 2004) was an American biochemist who helped to establish the role of DNA as the genetic material and contributed to the isolation and purification of the first antibiotics. His work on bacterial transformation helped lay the groundwork for the field of molecular genetics. Education Hotchkiss was born in South Britain, Connecticut. The son of factory workers, he attended Yale University after scoring the highest in the nation on an achievement test. Hotchkiss earned a B.S. in chemistry in 1932, and remained at Yale for a Ph.D. in organic chemistry. After completing his doctoral work in 1935, Hotchkiss became a fellow of the Rockefeller Institute of Medical Research, where he would remain until retirement in 1982. Research career At the Rockefeller Institute, Hotchkiss initially worked as an assistant to Oswald Avery and Walter Goebel, and was encouraged to learn more biology at a summer courses at the Marine Biological Laboratory. His early work isolating and synthesizing derivatives of glucoronic acid led to the identification of one of the specific polysaccharides in the capsule of type III pneumococci. Hotchkiss spent the 1937-1938 academic year in the lab of Heinz Holter and Kaj Linderstrøm-Lang at Carlsberg Laboratory learning protein analysis techniques. In 1938, he began collaborating with René Dubos to isolate and study antibiotics produced by soil bacteria. Their work on gramicidin and tyrocidine led to the first commercial antibiotics, and with Fritz Lipmann they found that the antibiotics include D-amino acids. During the late 1930s, Hotchkiss was also strongly critical of the Bergann–Niemann hypothesis of protein structure, the proposal by fellow Rockefeller biochemists Max Bergmann and Carl Niemann that protein structures always consist of multiples of 288 amino acids. (This would also be a feature of Dorothy Wrinch's cyclol hypothesis of protein structure).