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Scanning probe microscopy studies of...

Hurth, Cedric Michael.

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Scanning probe microscopy studies of active enzymes at solid surfaces.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Scanning probe microscopy studies of active enzymes at solid surfaces./
作者:	Hurth, Cedric Michael.
面頁冊數:	227 p.
附註:	Source: Dissertation Abstracts International, Volume: 67-04, Section: B, page: 2017.
Contained By:	Dissertation Abstracts International67-04B.
標題:	Chemistry, Analytical. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3215475
ISBN:	9780542649844

Scanning probe microscopy studies of active enzymes at solid surfaces.
Hurth, Cedric Michael.

Scanning probe microscopy studies of active enzymes at solid surfaces. - 227 p.

Source: Dissertation Abstracts International, Volume: 67-04, Section: B, page: 2017.

Thesis (Ph.D.)--The University of Texas at Austin, 2006.

This work is a study of active enzymes by several scanning probe microscopies in order to extract mechanical, electrochemical and electrical properties. It is divided into three parts. Atomic Force Microscopy (AFM) studies of yeast 3-phosphoglycerate kinase (PGK) ex situ and in situ is coupled to UV-visible spectrophotometry to compare the enzyme activity of the immobilized enzyme to that of the free enzyme. Glucose Oxidase and the decomposition of hydrogen peroxide are studied by Scanning Electrochemical Microscopy (SECM) to extract heterogeneous rate constant. Finally, Scanning Electrochemical Potential Microscopy (SECPM) is studied from an instrumentation-based point of view because it could be of use in the future.

ISBN: 9780542649844Subjects--Topical Terms:

586156
Chemistry, Analytical.

Scanning probe microscopy studies of active enzymes at solid surfaces.
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520 $a This work is a study of active enzymes by several scanning probe microscopies in order to extract mechanical, electrochemical and electrical properties. It is divided into three parts. Atomic Force Microscopy (AFM) studies of yeast 3-phosphoglycerate kinase (PGK) ex situ and in situ is coupled to UV-visible spectrophotometry to compare the enzyme activity of the immobilized enzyme to that of the free enzyme. Glucose Oxidase and the decomposition of hydrogen peroxide are studied by Scanning Electrochemical Microscopy (SECM) to extract heterogeneous rate constant. Finally, Scanning Electrochemical Potential Microscopy (SECPM) is studied from an instrumentation-based point of view because it could be of use in the future.
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