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Effective method for discriminating between oral bacterial and human alkaline phosphatase activity
Y Shibata1, Y Yamashita, H Miyazaki
1Department of Preventive Dentistry, Kyushu Dental College, Japan.
Oral Microbiology and Immunology
|February 1, 1994
Summary
Alkaline phosphatase (ALPase) activity in oral bacteria can be distinguished from human ALPase using sodium dodecyl sulfate (SDS). This method helps identify whether ALPase in gingival fluid originates from bacteria or a host response in periodontitis.
Area of Science:
- Microbiology
- Biochemistry
- Periodontology
Background:
- Alkaline phosphatase (ALPase) is an enzyme found in both oral bacteria and human tissues.
- Distinguishing the source of ALPase in gingival crevicular fluid is crucial for understanding periodontal disease.
- Bacterial and mammalian ALPase isoenzymes may exhibit different sensitivities to inhibitors.
Purpose of the Study:
- To quantitatively compare ALPase activity in various oral bacteria.
- To differentiate bacterial ALPase from mammalian ALPase using sodium dodecyl sulfate (SDS).
- To determine the origin of ALPase in gingival crevicular fluid in periodontitis patients.
Main Methods:
- Quantitative comparison of ALPase activity in different oral bacterial species.
- Assessing the effect of 1% sodium dodecyl sulfate (SDS) on bacterial and mammalian ALPase activity.
- Analyzing ALPase activity in gingival crevicular fluid from periodontitis patients.
Main Results:
- High ALPase activity was detected in periodontal bacteria: *Porphyromonas gingivalis*, *Prevotella intermedia*, and *Capnocytophaga sputigena*.
- Bacterial ALPase activity was significantly inhibited by 1% SDS, while mammalian ALPase isoenzymes were not.
- Gingival crevicular fluid from periodontitis patients showed a combination of SDS-sensitive (bacterial) and SDS-resistant (host) ALPase activities.
Conclusions:
- The SDS-based ALPase assay can effectively distinguish between bacterial and host-derived ALPase.
- ALPase activity in gingival crevicular fluid during periodontitis originates from both bacterial and host sources.
- This assay provides a valuable tool for diagnosing and understanding periodontal disease progression.