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Wakil, Biochim. Biophys. Acla 116, 189 (1966). i,p. W. Majcrus, A. W. Albcrts, and P. R. Vagelos, J. Biol. Chem. 240, 618 (1965). ~sp. W. Majerus, A. W. rts, and P. R. Vagelos, Proc. Natl. Acad. Sci. 8. 53~ 410 (1965). ~,. 20 Since the individual reactions of fatty acid synthesis are discussed in subsequent articles, only a few general comments will be made. Examination of Eqs. (2) to (7) indicates that two of them, Eqs. (2) and (3), are simple acyl transfers. It is not surprising that the enzymes catalyzing these reactions, acetyl-CoA-ACP transacylase and malonyl-CoA-ACP transacylase, are sulfhydryl proteins.
In the case of radioactive ACP the fractions may be assayed by measuring radioactivity. ~1 This step is the first in the purification procedure which requires assay. Depending on how the fractions from this column are pooled, the ACP content of the pooled eluate after this step of purification is 160-400 /~g per gram of protein. The pooled fractions may be concentrated either by acid precipitation or by batch elution from a small DEAE-cellulose column. Depending on the purity attained after this step, a second DEAE-cellulose column step may be required.
Larrabee, and G. P. Ailhaud, Federation Proc. 25, 1485 (1966). s F. Lynen, Federation Proc. 20, 941 (1961). *S. J. Wakil and J. Ganguly, J. Am. Chem. Soc. 81, 2597 (1959). ' R . Y. Hsu, G. Wasson, and J. W. Porter, J. Biol. Chem. 240, 3736 (1965). ' R. O. Brady, R. M. Bradley, and E. G. Trams, J. Biol. Chem. 235, 3093 (1960). o D. B. Martin, M. G. Homing, and P. R. Vagelos, J. Biol. Chem. 236, 663 (1961).  SATURATED FATTY ACID BIOSYNTHESIS IN E . coli 39 phosphate > inorganic phosphate. It was suggested that fructose 1,6diphosphate might act as an allosterie activator for the fatty acid synthesizing system in vivo.