Open Access. Powered by Scholars. Published by Universities.®
- Keyword
- Publication
- Publication Type
Articles 1 - 3 of 3
Full-Text Articles in Organisms
An Analysis Of Two Tests For Diesel Contamination In The Environment When Considering The Impact On Hydrocarbon Degrading Bacteria, Chris Wedding
An Analysis Of Two Tests For Diesel Contamination In The Environment When Considering The Impact On Hydrocarbon Degrading Bacteria, Chris Wedding
Mahurin Honors College Capstone Experience/Thesis Projects
No abstract provided.
Metal-Resistance Genetically Engineered Bacteria, Sylvia Daunert, Donna Scott, Sridhar Ramanathan
Metal-Resistance Genetically Engineered Bacteria, Sylvia Daunert, Donna Scott, Sridhar Ramanathan
KWRRI Research Reports
Bacterial-based electrochemical and optical sensing systems that respond in a highly selective and sensitive manner to antimonite and arsenite have been developed. This was accomplished by using genetically engineered bacteria bearing one of two plasmids constructed for our studies. The first plasmid, pBGD23, contains the operator/promoter region (O/P) and the gene of the ArsR protein from the ars operon upstream from the β-galactosidase gene. In the absence of antimonite/arsenite, ArsR binds to the 0/P site and prevents the transcription of the genes for ArsR and β-galactosidase, thus blocking expression of these proteins. When antimonite or arsenite is present in the …
In Vitro Plaque Formation On Orthodontic Resin Sealants, Leland W. Pack
In Vitro Plaque Formation On Orthodontic Resin Sealants, Leland W. Pack
Loma Linda University Electronic Theses, Dissertations & Projects
The purpose of this study was to examine in vitro plaque formation on sealant coated enamel. The plaque growth on different types of sealants placed on enamel was compared to each other and to an unsealed enamel control. The antimicrobial properties of sealants were also studied.
Sealant coated bovine enamel disks were immersed in a S. mutans culture medium for four days. The amount of bacterial plaque formation was quantified by removing the deposit, suspending it in solution with subsequent serial dilution. Aliquots of the dilutions were then spread on blood agar plates and incubated for 48 hours. The number …