Biomedical subjects
Publications and source records attributed to V D Kuznetsov.
Melanoid pigments are synthesized de novo when a mesophilic Streptomyces galbus Frommer culture is grown at an elevated temperature (42--47 degrees C). The pigments are accumulated in the mycelium walls whose thickness increases twofold.
Culture 78 was proposed as a neotype of Streptomyces ruber. It was isolated from the soils of the Baikal region and was closest, in its taxonomic properties, to the original description of the species [13] whose representative had been lost. Cultures from different microbial collections designated as S. ruber were shown to be unlike the original description. The neotype had the following taxononic properties: the cell wall of type I; spiral sporophores with extended spirals having 2-3 coils; oval spores with a smooth envelope; greyish pink aerial and dark-red substrate mycelia; a red pigment not passing into the medium; slow gelatin liquefaction and milk peptonization; weak starch hydrolysis; assimilation of glucose, xylose, rammose, fructose, and inositol; weak growth on arabinose, raffinose and mannitol, but not on sucrose; no formation of melanoid pigments; synthesis of riboflavin and prodigiosin pigments; inhibition of Gram-positive bacterial and acid-resistant mycobacterial growth; no inhibition of yeast and fungal growth. The culture was sensitive to streptomycin, neomycin, gentamycin, monomycin, tetracycline,erythromycin, oleandomycin, lincomycin, ristomycin, levomycetin, polymyxin and fusidin, but resistant in penicillin. The population was composed of six variants [3]: main, faded, asporogenic red, asporogenic yellow, asporogenic white and nocardia-like. The latter two were not capable of riboflavin and prodigiosin formation. The asporogenic yellow variant was a monosynthetic organism: it formed riboflavin, but could not synthesize prodigiosin. The neotype of S. ruber 78 is deposited withthe national Collection of Microorganisms (the reference number is VKM A-611).
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The culture of Streptomyces galbus ISP-5089 has a yellow-green colour caused by the accumulation of actinomycin X when it is grown in synthetic media at 28 degrees C; the colour turns dark-brown at 42 degrees C due to the synthesis of melanoid pigments. The population composition does not undergo any noticeable changes in that case, an no specific melanin-synthesizing mutants appear as a result of autoselection . The biosynthesis of actinomycin X (at 28 degrees C) and melanoid pigments (at 42 degrees C) is regulated by temperature. At 42 degrees C, L-DOPA oxidase is synthesized and laccase is activated; these two enzymes are involved in the synthesis of melanoid pigments. The organism does not has tyrosinase. The synthesis of melanoid pigments, when the mesophilic culture of S. galbus ISP-5089 is grown in the regime of superoptimal temperatures (42 to 47 degrees C), may be considered as a protective ecological reaction of the organism to unfavourable conditions of the environment.
The effect of inhibiting and stimulating agents on the biosynthesis of secondary metabolites (actinomycin X and melanoid pigments) was studied in Streptomyces galbus as a function of the growth temperature. D-Valine was shown to inhibit actinomycin synthesis and to stimulate production of melanoid pigments. Tryptophan stimulated the synthesis of both actinomycin and melanoid pigments. The temperature of growth was found to regulate the biosynthesis of secondary metabolites by the culture. The organism synthesized actinomycin at 28 degrees C, but it switched to the production of melanoid pigments at 42 degrees C. This may be considered as a protective reaction of the organism to an increase in the temperature of the environment and in UV radiation which is possible under natural conditions as a consequence of temperature elevation. The paper presents a hypothetical scheme for the regulation of biosynthesis of actinomycin and melanoid pigments by temperature. According to the scheme, the culture synthesizes secondary metabolites from tryptophan to hydroxykynurenine via a general pathway which is then bifurcated: at 28 degrees C--through methylhydroxyanthranilic acid to actinocin to actinomycin; at 42 degrees C--through hydroxyanthranilic acid, o-aminophenol, pyrocatechol, and possibly, o-benzoquinone, to melanin.