4.7 Article

The administration of l-cysteine and l-arginine inhibits biofilm formation in wild-type biofilm-forming yeast by modulating FLO11 gene expression

Journal

APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
Volume 103, Issue 18, Pages 7675-7685

Publisher

SPRINGER
DOI: 10.1007/s00253-019-09996-5

Keywords

Flor yeast; Adhesion to plastic; Phenotype microarray; Real-time PCR; FLO11

Funding

  1. Sardinia Regional Government through research grant (Regional Operational Program of the European Social Fund (ROP ESF))
  2. [10.5.12-C.U.P. J86C18000270002]

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Microbial biofilms are undesired in food manufacturing, drinking water distribution systems, and clinical realms. Yeast biofilms are particularly problematic because of the strong capacity of yeast cells to adhere to abiotic surfaces, cells, and tissues. Novel approaches have been developed over recent years to prevent the establishment of microbial biofilms, such as through the use of small molecules with inhibiting and dispersing properties. Here, we studied the inhibitory activity of 11 different amino acids on the biofilm formation ability of three wild-type Saccharomyces cerevisiae strains and the reference strain n-ary sumation 1278b. Subsequent evaluation of different concentrations of the two most effective amino acids, namely, arginine and cysteine, revealed that they acted in different ways. Arginine prevented biofilm formation by reducing FLO11 gene expression; its addition did not affect cell viability and was even found to enhance cell metabolism (vitality marker) as determined by phenotype microarray (PM) analysis. On the contrary, the addition of cysteine reduced both cell viability and vitality as well as FLO11 expression. Thus, the use of cysteine and arginine as agents against biofilm formation can be diversified depending on the most desired action towards yeast growth.

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