Efficiency of Phosphemide Employment at Increasing the Productivity of the Candida maltosa Tm-12 Strain

Tyumen State University Herald. Natural Resource Use and Ecology


Release:

2018, Vol. 4. №3

Title: 
Efficiency of Phosphemide Employment at Increasing the Productivity of the Candida maltosa Tm-12 Strain


For citation: Pak I. V., Trofimov O. V., Weisfeld L. I., Rustamov R. D., Skvortsova K. V. 2018. “Efficiency of Phosphemide Employment at Increasing the Productivity of the Candida maltosa Tm-12 Strain”. Tyumen State University Herald. Natural Resource Use and Ecology, vol. 4, no 3, pp. 69-80. DOI: 10.21684/2411-7927-2018-4-3-69-80

About the authors:

Irina V. Pak, Dr. Sci. (Biol.), Professor, Head of the Department of Ecology and Genetics, University of Tyumen; pakiv57@mail.ru

Oleg V. Trofimov, Cand. Sci. (Biol.), Assistant Professor, Department of Ecology and Genetics, University of Tyumen; oleg_v_trofimov@mail.ru

Larisa I. Weisfeld, Ph. D., Senior Researcher, N. M  Emanuel Institute of Biochemical Physics of the Russian Academy of Sciences (Moscow); liv11@yandex.ru

Rizvan D. Rustamov, Postgraduate Student, Department of Ecology and Genetics, University of Tyumen; kafedraekogen@mail.ru

Ksenia V. Skvortsova, Postgraduate Student, Department of Ecology and Genetics, University of Tyumen; kafedraekogen@mail.ru

Abstract:

A new way of increasing the productivity of the Candida maltosa Tm-12 yeast strain using phosphemide was invented. Phosphemide was developed at the All-Union Scientific Research Chemical-Pharmaceutical Institute and proposed as a cytostatic agent that suppresses the proliferation of tumor cells. Its mutagenic effect was demonstrated on the cultures of human and mouse fibroblasts, and on several plant species. The impact of various concentrations of phosphemide (0.1; 0.01; 0.001, and 0.0001%) on the Candida maltosa Tm-12 yeasts was examined. The research showed that the studied concentrations of phosphemide affect both the number and sizes of building up colonies. An effective phosphemide concentration providing 1,08 more increase in biomass than in the control was established. It was also shown that the studied concentrations of phosphemide bear no effect on the Candida maltosa Tm-12 protein composition.

References:

  1. Weisfeld L. I. 1965. “Cytogenetic Effect of Phosphazine on Human and Mouse Cells in Culture”. Russian Journal of Genetics, no 4, pp. 85-92.
  2. Russian National Collection of Industrial Microorganisms of the State Research Institute of Genetics and Selection of Industrial Microorganisms (“Genetika”). 2012. Passport of the Strain Candida maltosа Тм-12 (VKPM Y-612). 16 April. Moscow.
  3. Rapoport I. A 1977. “Dual Genetic Stimulation Induced by Supermutagens”. In: Mutational Selection, pp. 230-242. Moscow: Nauka Publishers.
  4. Chernov V. A. 1964. Employment of Cytotoxin Substances in the Chemotherapy of Malignant Tumors. Moscow: Meditsina.
  5. Aoyagi H., Katakura Y., Iwasaki A. 2016. “Production of Secretory Cutinase by Recombinant Saccharomyces cerevisiae Protoplasts”. Springer Plus, no 5, p. 160.
  6. Aruna A., Nagavalli M., Girijashankar V., Ponamgi S. P.D., Swathisree V., Venkateswar Rao L. 2015. “Direct Bioethanol Production by Amylolytic Yeast Candida albicans”. Letters in Applied Microbiology, vol. 65, no 3, pp. 229-236.
  7. Bome N. A., Bome A. Y., Ripberger E. I. 2015. “Ecological and Genetic Potential of Soft Spring Wheat in Conditions of the Northern Zauralye”. In: Biological Systems, Biodiversity, and Stability of Plant Communities, pp. 345-359. New Jersey: Apple Academic Press.
  8. Geiger M. R., Gibbons W. R., West T. P. 2014. “A Thermostable Candida molischiana Mutant Capable of Ethanol Production at Elevated Temperatures”. Journal of Pure and Applied Microbiology, vol. 8, no 2, pp. 1743-1748.
  9. Hara A., Ueda M., Misawa S., Matsui T., Furuhashi K., Tanaka A. 2000. “A Mutated Hygromycin Resistance Gene is Functional in the n-Alkane-Assimilating Yeast Candida tropicalis”. Archives of Microbiology, vol. 173, no 3, pp. 187-192. DOI: 10.1007/s002039900125
  10. Jung S., Park S. 2008. “Improving the expression of the Yield of Candida antarctica Lipase B in Escherichia coli by Mutagenesis’. Biotechnology Letters, vol. 30, no 4, pp. 717-722.
  11. Laemmli U. K. 1970. “Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4”. Nature, no 227, pp. 680-685.
  12. Oakley B. R., Kirsch D. R., Morris N. R. 1980. “A Simplified Ultrasensitive Silver Stain for Detecting Proteins in Polyacrylamide Gels”. Analytical Biochemistry, vol. 105, no 1, pp. 361-363.
  13. Radha Krishna E., Shamsher Kumar P., Veerendra Kumar B. 2011. “Strain of Selected Strain Bacillus subtilis (MTCC No.10619) for Enhanced Production of Antimicrobial Metabolites”. Journal of Microbiology and Biotechnology Research, vol. 1, no 3, pp. 32-38.
  14. Tamakawa H., Ikushima S., Yoshida S. 2012. “Efficient Production of l-Lactic Acid from Xylose by a Recombinant Candida utilis Strain”. Journal of Bioscience and Bioengineering, vol. 113, no 1, pp. 73-75.
  15. Weisfeld L. I. 2014. “About Cytogenetic Mechanism of Chemical Mutagenesis”. In: Opalko A. I., Weisfeld L. I., Bekuzarova S. A., Bome N. A., Zaikov G. E. (eds.). Ecological Consequences of Increasing Crop Productivity. Plant Breeding and Biotic Diversity, pp. 259-269. Toronto; New Jersey: Apple Academic Press.