Staphylococcus aureus
is a human pathogen that forms biofilm on catheters and medical implants. The authors' earlier study established that 1,2,3,4,6-penta-
O
-galloyl-β-D-glucopyranose (PGG) inhibits biofilm formation by
S. aureus
by preventing the initial attachment of the cells to a solid surface and reducing the production of polysaccharide intercellular adhesin (PIA). Our cDNA microarray and MALDI-TOF mass spectrometric studies demonstrate that PGG treatment causes the expression of genes and proteins that are normally expressed under iron-limiting conditions. A chemical assay using ferrozine verifies that PGG is a strong iron chelator that depletes iron from the culture medium. This study finds that adding FeSO
4
to a medium that contains PGG restores the biofilm formation and the production of PIA by
S. aureus
SA113. The requirement of iron for biofilm formation by
S. aureus
SA113 can also be verified using a semi-defined medium, BM, that contains an iron chelating agent, 2, 2′-dipyridyl (2-DP). Similar to the effect of PGG, the addition of 2-DP to BM medium inhibits biofilm formation and adding FeSO
4
to BM medium that contains 2-DP restores biofilm formation. This study reveals an important mechanism of biofilm formation by
S. aureus
SA113.
This paper utilizes the recently defined equivalent noise sheet resistance to study the noise perfonnance of fu ture sub-lOOnm MOSFETs using strain engineering, channel engineering with III -V materials, and quantum well structures for low-noise applications. Experimental results for devices fabricated in UMC's five different CMOS technology nodes and other published data down to 20 nm technology node are demonstrated. Strategies for the future low-noise technologies are also discussed.
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