Evaluation of partially purified cholesterol esterase for clinical assay of cholesterol
Issued Date
1989
Copyright Date
1989
Resource Type
Language
eng
File Type
application/pdf
No. of Pages/File Size
iv, 61 leaves : ill.
Access Rights
open access
Rights
ผลงานนี้เป็นลิขสิทธิ์ของมหาวิทยาลัยมหิดล ขอสงวนไว้สำหรับเพื่อการศึกษาเท่านั้น ต้องอ้างอิงแหล่งที่มา ห้ามดัดแปลงเนื้อหา และห้ามนำไปใช้เพื่อการค้า
Rights Holder(s)
Mahidol University
Bibliographic Citation
Thesis (M.Sc. (Biochemistry))--Mahidol University, 1989
Suggested Citation
Koson Sim Evaluation of partially purified cholesterol esterase for clinical assay of cholesterol. Thesis (M.Sc. (Biochemistry))--Mahidol University, 1989. Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/103297
Title
Evaluation of partially purified cholesterol esterase for clinical assay of cholesterol
Alternative Title(s)
การประเมินคุณค่าของเอนไซม์โคเลสเตอรอลเอสเตอเรสเพื่อใช้ในการวิเคราะห์โคเลสเตอรอลในโรงพยาบาล
Author(s)
Advisor(s)
Abstract
Bhinyo Panijpan ths."Serum cholesterol determination is a routine diagnostic method for arteriosclerosis. The enzymatic determination of cholesterol requires three enzymes, namely, cholesterol esterase, cholesterol oxidase and peroxidase. The objective of this project was to investigate a new source of cholesterol esterase suitable for diagnostic application. Forty five isolates of bacteria and sixteen isolates of moulds were screened for extracellular cholesterol esterase. The isolate that produced the highest yield of the enzyme was selected and was identified as Pseudomonas sp. based on Bergey's manual. The enzyme was partially purified by 2 methods: one method by the combination of DEAE-cellulose column and Sephadex G-200 gel column chromatography, and the other method by calcium chloride precipitation. The purification fold of the enzyme were about 24 and 13 respectively. The specific activity of the partially purified enzyme was about 1.2 unit/mg protein with 75% recovery for both methods of purification. The partially purified enzyme was studied for its physical and biochemical properties, and the results were the followings: molecular weight was about 600,000 daltons by gel filtration, pH optimum 7.0-9.0, temperature optimum 50 degree C, pH stability in the range 5.0-10.0, K(,m) value 3.3x10 (-5) M, stable at 4 degree C and in frozen condition for at least 2 months, the enzyme was able to hydrolyze serum cholesterol esters to the same extent as alkaline hydrolysis. These results suggest that cholesterol esterase from this pseudomonad was potentially suitable for further development in diagnostic application.
Description
Biochemistry (Mahidol University 1989)
Degree Name
Master of Science
Degree Level
Master's degree
Degree Department
Faculty of Science
Degree Discipline
Biochemistry
Degree Grantor(s)
Mahidol University