Quantitative proteomics analysis reveals an important role of the transcriptional regulator UidR in the bacterial biofilm formation of .

INTRODUCTION

Bacterial biofilm is a well-known characteristic that plays important roles in diverse physiological functions, whereas the current intrinsic regulatory mechanism of its formation is still largely unknown.

METHODS

In the present study, a label-free based quantitative proteomics technology was conducted to compare the differentially expressed proteins (DEPs) between and the wild-type strain in the biofilm state.

RESULTS

The results showed that the deletion of gene uidR encoding a TetR transcriptional regulator significantly increased the biofilm formation in . And there was a total of 220 DEPs, including 120 up-regulated proteins and 100 down-regulated proteins between and the wild-type strain based on the quantitative proteomics. Bioinformatics analysis suggested that may affect bacterial biofilm formation by regulating some related proteins in glyoxylic acid and dicarboxylic acid pathway. The expressions of selected proteins involved in this pathway were further confirmed by q-PCR assay, and the results was in accordance with the quantitative proteomics data. Moreover, the deletion of four genes ( and ) related to the glyoxylic acid and dicarboxylic acid pathway lead to a significant decrease in the biofilm formation.

DISCUSSION

Thus, the results indicated that involved in the regulatory of bacterial biofilm formation, and it may provide a potential target for the drug development and a new clue for the prevention of pathogenic in the future.