现代农业科技
現代農業科技
현대농업과기
XIANDAIHUA NONGYE
2012年
10期
41-44,46
,共5页
徐雯映%彭子强%朱晓明%郑荣威%伍志权
徐雯映%彭子彊%硃曉明%鄭榮威%伍誌權
서문영%팽자강%주효명%정영위%오지권
酵母蔗糖酶%金属离子%修饰酶%动力学%光谱分析
酵母蔗糖酶%金屬離子%脩飾酶%動力學%光譜分析
효모자당매%금속리자%수식매%동역학%광보분석
yeast intervase%metal ion%modified enzyme%kinetics analysis%spectrum analysis
以不同浓度EDTA、Mn2+.Zn2+和Fe2+为效应物,以蔗糖为底物,研究EDTA和金属离子对酵母蔗糖酶(Yeastinvertase)天然酶和修饰酶催化活性的影响。结果表明:EDTA对天然酶和修饰酶均有抑制作用。Mn2+对天然酶和修饰酶有激活作用;Zn2+和Fe2+对天然酶有抑制作用.对修饰酶有激活作用。动力学分析显示,经5mmol/LEDTA、Mn2+.Zn2+和Fe2+处理后,天然酶和修饰酶的Km和Vmax值均发生变化。光谱分析显示.经不同浓度EDTA和Fe2+处理后,天然酶和修饰酶的构型构象发生变化;经不同浓度Mn2+和Zn2+处理后,天然酶和修饰酶的构型构象基本上没有发生变化。
以不同濃度EDTA、Mn2+.Zn2+和Fe2+為效應物,以蔗糖為底物,研究EDTA和金屬離子對酵母蔗糖酶(Yeastinvertase)天然酶和脩飾酶催化活性的影響。結果錶明:EDTA對天然酶和脩飾酶均有抑製作用。Mn2+對天然酶和脩飾酶有激活作用;Zn2+和Fe2+對天然酶有抑製作用.對脩飾酶有激活作用。動力學分析顯示,經5mmol/LEDTA、Mn2+.Zn2+和Fe2+處理後,天然酶和脩飾酶的Km和Vmax值均髮生變化。光譜分析顯示.經不同濃度EDTA和Fe2+處理後,天然酶和脩飾酶的構型構象髮生變化;經不同濃度Mn2+和Zn2+處理後,天然酶和脩飾酶的構型構象基本上沒有髮生變化。
이불동농도EDTA、Mn2+.Zn2+화Fe2+위효응물,이자당위저물,연구EDTA화금속리자대효모자당매(Yeastinvertase)천연매화수식매최화활성적영향。결과표명:EDTA대천연매화수식매균유억제작용。Mn2+대천연매화수식매유격활작용;Zn2+화Fe2+대천연매유억제작용.대수식매유격활작용。동역학분석현시,경5mmol/LEDTA、Mn2+.Zn2+화Fe2+처리후,천연매화수식매적Km화Vmax치균발생변화。광보분석현시.경불동농도EDTA화Fe2+처리후,천연매화수식매적구형구상발생변화;경불동농도Mn2+화Zn2+처리후,천연매화수식매적구형구상기본상몰유발생변화。
EDTA and different metal ions were used as effectors,and sucrose as substrate in order to study the effects of EDTA and different metal ions on enzyme specific activity of yeast invertase and its modified enzyme.The metal ions included Mn2+,Zn2+ and Fe2+.The results showed that the treatment of EDTA restrained the activity of natural enzyme and modified enzyme.Mn2+ activated the activity of natural enzyme and its modified enzyme. Zn2+ and Fe2+ activated the activity of modified enzyme but restrained natural enzyme.Kinetic analysis showed that the value of Km and Vmax changed after the treatment of 5 mmol/L EDTA and different metal ions.The spectral analysis showed that the configuration and conformation of natural enzyme and modified enzyme were changed after the treatment of EDTA and Fe2+.However, after the treatment of Mn2. and Zn2+,the configuration and conformation of natural enzyme and modified enzyme did not change.