Title: 硫胱胺基酸氧化與酚亞硫酸基轉移酵素穩定性關係之探討
Effects of Cysteine Oxidation on the Stability of Phenol Sulfotransferase
Authors: 劉思秀
Liu, Szu- Hsiu
楊裕雄
Yuh-Shyong Yang
生物科技學系
Keywords: 酚亞硫酸基轉移酵素;硫胱胺基酸;氧化還原;穩定性;Phenol sulfotransferase;Cysteine;Oxidation;Stability
Issue Date: 1997
Abstract: 酚亞硫酸基轉移酵素是一個解毒酵素,在生物體內主要負責亞硫酸基
的轉移,具有相當重要的功能。此酵素內含五個cysteine,這些cysteine
在酵素中所扮演的角色目前並不清楚。我們利用各種物理和化學方式對野
生株及cysteine突變株進行研究,希望能了解當單一個cysteine突變為
serine時,對酵素的活性是否有影響,並且希望能找出使酵素更穩定的方
法,以利未來進行此與酵素有關之研究。實驗結果發現:(1)在氧化還原
實驗中,將酚亞硫酸基轉移酵素以氧化劑處理,野生株及突變株之酵素同
樣會受氧化劑影響,而且在酵素氧化的過程中可以明顯觀察到:酚亞硫酸
基轉移酵素的b型酵素會先改變活性,a型酵素的活性則維持一段時間才變
化;以GSH及DTT兩種不同還原劑去處理野生株以及突變株,發現還原劑對
不同酵素的影響相同,且不同還原劑對酵素活性會有不同的影響。(2)在
酵素穩定性實驗中,以nucleotides、 glycerol、EDTA、sucrose保護野
生株及突變株酵素,發現這些試劑都能穩定酵素,而且將酵素放置在含
有100 mM Bis-Tris propane (pH 7.0),1 mM DTT,1 mM EDTA,10 %
(v/v) glycerol , 125 mM sucrose , 0.5 mM adenosine的4℃環境中,
會使酵素活性維持三星期以上。
Phenol sulfotransferase, a member of the enzyme of
detoxification, plays a very important role in biological
system. There are five cysteine residues in phenol
sulfotransferase, but their function is not clear. To understand
the effects of cysteine on the enzyme activity, we used various
physical or chemical methods to treat wild type and cysteine
mutants of phenol sulfotransferase. The results indicate the
following. (1) Oxidation of wild type and mutants by GSSG
affecttheir enzymatic activity. During the process of oxidation,
we observedthat the b-form phenol sulfotransferase responded
quickly with changes in the activity profile upon incubation
with oxidation. The activityof the a-form enzyme was changed
after a longer incubation period. However incubation with
different reducing reagents, these enzymes have different
effects. (2) We used a variety of compounds, such as
nucleotides, glycerol, EDTA and sucrose, to stabilize the wild
type and mutant phenol sulfotransferase. These regents protect
these enzymes from oxidation. We found that the enzyme is stable
for at least three weeks under the incubation conduction : 100
mM Bis-tris-propane at pH 7.0, 1 mM EDTA, 10% (v/v) glycerol,
125 mM sucrose, 0.5 mM adenosine at 4℃.
URI: http://140.113.39.130/cdrfb3/record/nctu/#NT860111007
http://hdl.handle.net/11536/62586
Appears in Collections:Thesis