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  5. Capturing More Light: Phycobilisome Characterization for Increased Hydrogen Production Efficiency
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Capturing More Light: Phycobilisome Characterization for Increased Hydrogen Production Efficiency

Date Issued
May 1, 2012
Author(s)
Willard, Paul Abraham
Advisor(s)
Barry D. Bruce
Additional Advisor(s)
Paul Frymier, Eric Boder
Abstract

Alternative energy and biofuels are a growing area of research. The demand for more and clean energy is ever increasing, but the current technology is inefficient, expensive, and incapable of meeting the demands of the current market. Hydrogen is a potential future fuel, as it is both clean and renewable, but its formation through conventional means is costly and inefficient. Photosynthesis can be utilized for the formation of hydrogen, which can then serve as a convenient and renewable biofuel. Photosynthetic hydrogen evolution is observed in vitro, but the current photosystem design is not very versatile and optimized to use all incident light it may receive from the sun. Manipulating the photosynthetic machinery by adding phycobilisomes, light-absorbing antennae, to the in vitro system, can potentially boost the absorption and utilization of light available to this system.


To make use of phycobilisomes in this system, a careful look at the structural stability and dissociation pathway of the complex into smaller pieces is pursued to isolate the desired phycobilisome rod component. These rod components are ideal for utilization because of their natural ability to transfer energy to the photosystem, but the organisms from which they are isolated do not preferentially produce them. In addition, a mechanism by which phycobilisome rods can attach to the designed hydrogen evolving system and the completed preparative molecular biology work is presented.

Subjects

Phycobilisome

Dissociation

Hydrogen Evolution

Photosystem I

Fusion Protein

Disciplines
Biochemical and Biomolecular Engineering
Biochemistry
Degree
Master of Science
Major
Chemical Engineering
File(s)
Thumbnail Image
Name

Thesis_Final_PaulW.pdf

Size

20.27 MB

Format

Adobe PDF

Checksum (MD5)

df704a79dba8ab79facded7888c5636f

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