下載電子全文宣告This thesis is authorized to indicate in-campus access at one year and off-campus not accessible
You can not download at the moment.
Your IP address is 22.214.171.124
The defense date of the thesis is 2005-03-31
The current date is 2018-06-18
This thesis will be accessible at off-campus not accessible
URN etd-0331105-144525 Statistics This thesis had been viewed 2116 times. Download 23 times. Author Hui-Min Lin Author's Email Address No Public. Department Bioengineering Year 2004 Semester 1 Degree Master Type of Document Master's Thesis Language English Page Count 141 Title STUDY ON THE PHA BIOSYNTHESIS IN HALOPHILIC Haloferax mediterranei Keyword PHA halophilic Haloferax mediterranei Haloferax mediterranei halophilic PHA Abstract This study is focus on the variation of activities for PHA synthase and PHA depolymerase as well as the PHA biosynthesis in the fermentation of haliphilic Haloferax mediterranei.
H. mediterranei was cultured in shacking culture with the glucose, extructed bran/starch, or n-butanic acid as carbon sources. Above 0.1 % n-butanic acid would inhibited the growth of H. mediterranei. The extructed bran/starch was the most favorable carbon source for this bacterial growth and it had higher activity of PHA synthase but lower of PHA depolymerase. In the fermentation of continuous feeding-batch controlled by pH-stat, the activity curves for PHA synthase and PHA depolymerase were similar to the growth curve but delayed for a few hours. Using liquid culture as starter for the fermentation of continuous feeding- batch, it took 50 hrs to the maximum of cell dry weight and was only the half of time by using the suspension of colony from plate. It also had higher activity of PHA synthase than activity of PHA depolymerase. However, the CDW, PHA amount, and PHA content were lower. It showed that the biosynthesis of PHA was related to the bacterial physiologic state and PHA-related enzymes were expressed at late exponential phase.
It was failure to merge the peptide sequences of PHB granule bound proteins obtained from the sequencing results by Q-TOF. The PHB relative enzymes had been partially purified, but the recovery of these enzymes activities were very low after ultracentrifugaion due to their unstability in purification procedure. It is necessary to study the enzyme stability in future.
Advisor Committee Ming-Tse Lin - advisor
none - co-chair
none - co-chair
Files Date of Defense 2004-01-26 Date of Submission 2005-03-31