- 1) Ibears, J. I., Lozano, I., Perdigones, F., and Jimenez, J., Dynamics of ‘flor’ yeast populations during the biological ageing of sherry wines. Am. J. Enol. Vitic., 48, 75–79 (1997).
- 2) Zara, S., Farris, G. A., Budroni, M., and Bakalinsky, A. T., HSP12 is essential for biofilm formation by a Sardinian wine strain of S. cerevisiae. Yeast, 19, 269–276 (2002).
- 3) Cantarelli, C., and Martini, A., On the pellicle formation by ‘flor’ yeasts. Antonie van Leeuwenhoek. Suppl. Yeast Sympos., 35, F35–F36 (1969).
- 4) Iimura, Y., Hara, S., and Otsuka, K., Cell surface hydrophobicity as pellicle formation factor in a film strain of Saccharomyces. Agric. Biol. Chem., 44, 1215–1222 (1980).
- 5) Iimura, Y., Hara, S., and Otsuka, K., Fatty acids as hydrophobic substance on cell surface of film strain of Saccharomyces. Agric. Biol. Chem., 44, 1223–1229 (1980).
- 6) Ishigami, M., Nakagawa, Y., Hayakawa, M., and Iimura, Y., FLO11 is essential for flor formation caused by the C-terminal deletion of NRG1 in Saccharomyces cerevisiae. FEMS Microbiol. Lett., 237, 425–430 (2004).
- 7) Zara, S., Bakalinsky, A. T., Zara, G., Pirino, G., Demontis, M. A., and Budroni, M., FLO11-based model for air-liquid interfacial biofilm formation by Saccharomyces cerevisiae. Appl. Environ. Microbiol., 71, 2934–2939 (2005).
- 8) Sambrook, J., Fritsch, E. F., and Maniatis, T., Molecular cloning: a laboratory manual, 2nd ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor (1989).
- 9) Rose, M., Winston, F., and Hieter, P., Methods in yeast genetics: a laboratory manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor (1990).
- 10) Brachmann, C. B., Davies, A., Cost, G. J., Caputo, E., Li, J., Hieter, P., and Boeke, J. D., Designer deletion strain derived from Saccharomyces cerevisiae S288C: a useful set of strains and plasmids for PCR-mediated gene disruption and other applications. Yeast, 14, 115–132 (1998).
- 11) Yamazaki, T., Kaneko, Y., Harashima, S., and Oshima, Y., Correlation between sulfur dioxide tolerance of a wine yeast strain of Saccharomyces cerevisiae and its chromosome XVI mobility in pulsed-field gradient gel electrophoresis. J. Brew. Soc. Jpn., 91, 640–643 (1995).
- 12) Wach, A., PCR-synthesis of marker cassettes with long flanking homology regions for gene disruptions in S. cerevisiae. Yeast, 12, 259–265 (1996).
- 13) Goldstein, A. L., and McCusker, J. H., Three new dominant drug resistance for gene disruption in Saccharomyces cerevisiae. Yeast, 15, 1541–1553 (1999).
- 14) Misu, K., Fujimura-Kamada, K., Ueda, T., Nakano, A., Katoh, H., and Tanaka, K., Cdc50p, a conserved endosomal membrane protein, controls polarized growth in Saccharomyces cerevisiae. Mol. Biol. Cell, 14, 730–747 (2003).
- 15) Gietz, R. D., and Woods, R. A., High efficiency transformation with lithium acetate. In “Molecular Genetics of Yeast, A Practical Approach,” ed. Johnson, J. R., IRL Press, Oxford, pp. 121–134 (1994).
- 16) Ito, H., Fukuda, Y., Murata, K., and Kimura, A., Transformation of intact yeast cells treated with alkali cations. J. Bacteriol., 153, 163–168 (1983).
- 17) Hereford, L., Fahrner, K., Woodford, J., Jr., Rosbash, M., and Kaback, D. B., Isolation of yeast histone genes H2A and H2B. Cell, 18, 1261–1271 (1979).
- 18) Elder, R. T., Loh, E. Y., and Davis, R. W., RNA from the yeast transposable element Ty1 has both ends in the direct repeats, a structure similar to retrovirus RNA. Proc. Natl. Acad. Sci. USA, 80, 2432–2436 (1983).
- 19) Park, S. H., Kho, S. S., Chun, J. H., Hwang, H. J., and Kang, H. S., Nrg1 is a transcriptional repressor for glucose repression of STA1 gene expression in Saccharomyces cerevisiae. Mol. Cell. Biol., 19, 2044–2050 (1999).
- 20) Vyas, V. K., Kuchin, S., and Carlson, M., Interaction of the repressors Nrg1 and Nrg2 with the Snf1 protein kinase in Saccharomyces cerevisiae. Genetics, 158, 563–572 (2001).
- 21) Zhou, H., and Winston, F., NRG1 is required for glucose repression of the SUC2 and GAL genes of Saccharomyces cerevisiae. BMC Genet., 2, 5 (2001).
- 22) Lo, W. S., and Dranginis, A. M., FLO11, a yeast gene related to the STA genes, encodes a novel cell surface flocculin. J. Bacteriol., 178, 7144–7151 (1996).
Full access
FLO11 Is the Primary Factor in Flor Formation Caused by Cell Surface Hydrophobicity in Wild-Type Flor Yeast
Reprints and Corporate Permissions
Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?
To request a reprint or corporate permissions for this article, please click on the relevant link below:
Academic Permissions
Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?
Obtain permissions instantly via Rightslink by clicking on the button below:
If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.
Related research
People also read lists articles that other readers of this article have read.
Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.
Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.