CHARACTERISATION OF AN ANTARCTIC YEAST, Glaciozyma antarctica PI12

Authors

  • Teoh Chul Peng Biotechnology Research Institute, Universiti Malaysia Sabah, Kota Kinabalu, Sabah, Malaysia
  • Koh Soon Peng Biotechnology Research Institute, Universiti Malaysia Sabah, Kota Kinabalu, Sabah, Malaysia
  • Clemente Michael Wong Vui Ling Biotechnology Research Institute, Universiti Malaysia Sabah, Kota Kinabalu, Sabah, Malaysia

DOI:

https://doi.org/10.51200/bijb.v1i.2154

Keywords:

cell morphologies, bipolar budding, yeast chain, quiescence state, hydrolytic enzyme, Antarctic yeast, Glaciozyma spp, enzyme activities, psychrophiles

Abstract

Glaciozyma antarctica PI12 is a psychrophilic yeast isolated from Antarctica. It has an optimal growth in yeast peptone dextrose (YPD) and yeast mould (YM) broth media but not in potato dextrose (PD) broth medium. Early phase G. antarctica PI12 cells had elongated-shape and became oval-shaped as they aged. G. antarctica PI12 exhibited bipolar budding and formed a chain of cells during the lag and early exponential phases. The number of chains decreased as the yeast aged. It appeared mainly as a single cell at the stationary phase, and a small number of them still produced buds. Some cells at the stationary phase entered the quiescence state (G0) as a longterm survival strategy. The G. antarctica PI12 cell size decreased when they entered the stationary phase. G. antarctica PI12 was found to produce hydrolytic enzymes, chitinase, cellulase, mannanase, and xylanase. A higher glucose concentration of 2% in the PD agar medium inhibited the activities of chitinase but not the cellulase, mananase and xylanase.

References

Alias, N., Mazian, A., Salleh, A. B., Basri, M., & Rahman, R. N. Z. R. A. (2014). Molecular cloning and optimization for high level expression of cold-adapted serine protease from Antarctic yeast Glaciozyma antarctica PI12. Enzyme Research, (2014), 1 – 20.

Boo, S. Y., Wong, C. M. V. L., Rodrigeus, K. F., Najimudin, N., Murad, A. M. A., & Mahadi, N. M. (2013). Thermal stress responses in Antarctica yeasts, Glaciozyma antarctica PI12, characterized by real-time quantitative PCR. Polar Biology, 36, 381 – 389.

Brenchley, J. E. (1996). Psychrophilic microorganisms and their cold-active enzymes. Journal of Industrial Microbiology, 17 (5 – 6), 432 – 437.

Carrasco, M., Rozas, J. M., Baahona, S., Alcalno, J., Cifuentes, V., & Beaze, M. (2012). Diversity and extracellular enzymatic activities of yeasts isolated from King George Island, the sub- Antarctic region. BMC Microbiology, 12, 251.

Connell, L., Redman, R., Craig, S., Scorzetti, G., Iszard, M., & Rodriguez, R. (2008). Diversity of soil yeasts isolated from South Victoria Land, Antarctica. Microbial Ecology, 56 (3), 448 – 459.

Donachie, S. P. (1995). Ecophysiological description of marine bacteria from Admiralty Bay (Antarctica), and the digestive tracts of selected Euphausiidae (Doctoral Thesis). Polish Academy Sciences, Warsaw.

Fell, J. W., Statzell, A. C., Hunter, I. L., & Phaff, H. J. (1969). Leucosporidium gen. n., the heterobasidiomycetous stage of several yeasts of the genus Candida. Antonie van Leeuwenhoek, 35 (1), 433 – 462.

Feller, G., & Gerday, C. (1997). Psychrophilic enzymes: Molecular basis of cold adaptation. Cellular and Molecular Life Sciences CMLS, 53 (10), 830 – 841.

Firdaus, R. M., Hashim, N. H. F., Bharudin, I., Bakar, M. F. A., Huang, K. K., Alias, H., … Tay, L. J. (2018). The Glaciozyma antarctica genome reveals an array of systems that provide sustained responses towards temperature variations in a persistently cold habitat. PloS One, 13 (1).

Galdieri, L., Mehrotra, S., Yu, S., & Vancura, A. (2010). Transcriptional regulation in yeast during diauxic shift and stationary phase. Omics: A Journal of Integrative Biology, 14 (6), 629 – 638.

Golubev, V. I., Blagodatskya, V. M., Manukian, A. R., & Liss, O. L. (1981). The yeast floras of peat (in Russia). Izvestila Akademii Nauk SSSR, Serila Biologicheskaia, 181 – 187.

Gray J. V., Petsko, G. A., Johnston, G. C., Ringe, D., Singer, R. A., & Werner-Washburne, M. (2004). “Sleeping Beauty”: Quiescence in Saccharomyces cerevisiae. Microbiology and Molecular Biology Review, 68 (2), 187 – 206.

Johnston, G. C., Pringle, J. R., & Hartwell, L. H. (1977). Coordination of growth with cell division in the yeast Saccharomyces cerevisiae. Experimental Cell Research, 105 (1) 79 – 98.

Koh, J. S. P., Wong, C. M. V. L., Najimudin, N., & Mahadi, N. M. (2019). Gene expression patterns of Glaciozyma antarctica PI12 in response to cold, and freeze stress. Polar Science, 20, 45 – 54.

Kockova-Kratochvilova, A., Wegener, K. A., & Ondrusova, D. (1972). Ein-Beitrag zur okologie der Hefen aus Nordost-Mecklenburg. Mycopathologia Et Mycologia Applicata, 48, 191 – 212.

Lodish, H., Berk, A., Zipursky, S. L., Matsudaira, P., Baltimore, D., & Darnell, J. (2000). Molecular cell biology (4th edition). New York: W. H. Freeman.

Powell, C. D., Zandcyke, S. M. V., Quain, D. E., & Smart, K. A. (2000). Replicative ageing and senescence in Saccharomyces cerevisiae and the impact on brewing fermentations. Microbiology, 146, 1023 – 1034.

Pueschel, M. (2013). SEM-Specimen preparation and techniques. Retrieved from http://australianmuseum.net.au/Specimen-preparation-and-techniques.

Ramli, A. N., Mahadi, N. M., Rabu, A., Murad, A. M., Bakar, F. D., & Illias, R. M. (2011). Molecular cloning, expression and biochemical characterisation of a cold-adapted novel recombinant chitinase from Glaciozyma antarctica PI12. Microbial Cell Factories, 10 (1), 94.

Published

2020-12-23

How to Cite

Teoh Chul Peng, Koh Soon Peng, & Clemente Michael Wong Vui Ling. (2020). CHARACTERISATION OF AN ANTARCTIC YEAST, Glaciozyma antarctica PI12. Borneo International Journal of Biotechnology (BIJB), 1, 89–102. https://doi.org/10.51200/bijb.v1i.2154
Total Views: 515 | Total Downloads: 433