In an attempt to examine the specific metabolic relationship between the alkane substrates and lipid products the pattern of formation of cellular lipid, especially fatty acids, has been studied in the coursu of incubation of cells of C. rugosa with n-alkanes in mineral medium. cis:^, Ci8:i, Ci6:i and Ci6:o fatty acids were the major products formed, irrespective of the odd or even chain length of the alkane used as substrate. These unsaturated fatty acids reached a maximum in the stationary phase. In the case of cells grown on odd-chain n-alkanes (from C,, t o C,,), the proportion of odd-chain cellular fatty acids was markedly high, reaching 77 -88y0 in the n-pent& decane and heptadecane-grown cells. The resulting acids are then metabolized by 8-oxidation or inserted directly or after elongation with C,-units into the cellular fatty acids. The total lipid content of n-alkane (n-C,o-C!20) grown cells in the stationary phase was 16.3-19.0y0 of the dry cell weight, which was about three times as much as that of glucose-grown cells. The chain length of alkane substrates had a significant effect on the lipid content. Ergosterol production from n-hexadecane was twice higher than that from glucose.Fatty acids and fatty acid esters are the most significant direct products of n-alkane metabolism in microorganisms. Hence, numerous reports have appeared describing qualitative and quantitative aspects of cellular lipids in microorganisms grown on n-alkane in an attempt t o obtain the specific metabolic relationship between the alkane substrates and lipid products (DAVIS 1964, DUNLAP and PERRY 1967, NYNS et al. 1968, MISHINA et al. 1973, HUG and BIECHTER 1973, PATRIK and DUGAN 1974.Quality and quantity of cellular fatty acids formed from n-alkanes, however, are greatly influenced by the type of organism and alkane substrate. Since 1956, we have studied the microbial assimilation mechanism of hydrocarbons. We have described the initial oxidation of decane by Candida rugosa JFlOl (IIDA and IIZUKA 1971). I n 1974 we reported the biosynthesis of extracellular monosaccharides from hydrocarbon and the structure of cell wall mannan of n-alkane-grown cells (IIDA and FINNERTY 1974a, b). More recently, we reported on the microbodiea of the hydrocarbon-assimilating yeast, C. rugosa (TANAKA and IIDA 1977).This investigation details the nature and diversity of fatty acids derived from C. rugosa growing a t the expense of a homologous series of odd and even n-alkanes as sole carbon and energy source.
Materials and methodsCultivation: The organism used was Candida rugosa JFlO1, which was grown in an inorganic salt medium (pH 7.2) (IIDA and FINNERTY 1974a) containing 1% (v/v) hydrocarbon or 1% (w/v) glucose and sodium acetate. The incubation was carried out a t 27 "C in a 500 ml conical flask containing 100 ml medium on a rotary shaker (220 rpm). The 12 straight-chain n-alkanes used were 99% pure and purchased from Tokyo Chemical Co., Ltd.Assay of cellular fatty acids: The whole cells were collected a t the exponential phase and the Statio...