Amino acids are considered to be the most easily assimilable metabolites. Like other organisms, fungi also utilize the majority of the amino acids as such in their amino acid pool. Recent evidences, however, indicate conversion of amino acids into ammonia before their utilization by fungi. This conversion depends upon the oxidative deamination of amino acids by oxidases which are the flavoproteins. In the present work an attempt has been made to determine the comparative efficiency and rate of consumption of some of the common ammo acids. The pathway of assimilation, however, has not been studied. The following amino acids were employed: Glycine, DL-valine, DL-a-alanine, DLphenylalanine, L-aspartic acid, L-glutamic acid, L-asparagin, L-histidine, L(-)-cystine, DL-methionine, DL-serine, DL-lysine and L( + )arginine.
Materials and MethodsThe three organisms Pestalotia paiiciseta Sacc, Botryodiplodia theobromae Pav. and Colletotrichum gloeosporioides Penz., isolated from leaf spots of Nephelium litchi Camb. (PRASAD 1962), were used in the present investigations. Inoculations were made by GARRETT'S (1936) agar disc method from 7-12 days old cultures. Chemicals supplied by E.Merck or B.D.H. were used and all media were prepared in double distilled water. Glasswares exclusively of Pyrex make were used for distillation. 25 ml of sterilized media contained in 150 ml Erlenmeyer flasks served as nutrient in each case. Different amino acids were substituted singly for 3.5 g of KNOg/litre of modified ASTHANA and HAWKER'S medium A containing 10 g of glucose. All the inoculated flasks were incubated simultaneously at room temperature. The mean laboratory temperature during the period of incubation was 23 °C. pH of all media was adjusted to 6.0 as this pH was found to be the most suitable for growth of all the three pathogens. The dry weights of fungal mats of three different ages i.e. after 5, 10 and 15 days served as quantitative measure of growth. Three replicates were used for each series and their average has been taken as standard value. The dry weight results were statistically analysed. One set of 15 flasks of eadi treatment was separated for diromatographic analysis to detect the presence of various ammo acids. Circular paper chromatographie technique described by RANJAN et al. (1955) was used for this purpose. Butanol-acetic acid-water (4:1:5) was used as solvent, while 0.01 g ninhydrin dissolved in n-butanol served as spray reagent.