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应用果聚糖蔗糖酶(Levansucrase)系统使MuIFN-α-7基因在枯草芽孢杆菌中表达
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作者 陈玉梅 《生物技术通报》 CAS CSCD 1990年第5期78-78,共1页
用寡核苷酸位点定向诱变法除去基因的信号肽序列,然后将这个基因克隆于蛋白质分泌载体质粒pC194中。
关键词 基因克隆 枯草芽孢杆菌 levansucrase MuIFN-α-7 果聚糖 载体质粒 蔗糖酶 启动子 定向诱变 信号肽序列
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Enhancing levan biosynthesis by destroying the strongly acidic environment caused by membrane-bound glucose dehydrogenase(mGDH)in Gluconobacter sp.MP2116
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作者 Junjie Tian Shumin Wei +1 位作者 Wenxing Liang Guangyuan Wang 《Synthetic and Systems Biotechnology》 2025年第1期68-75,共8页
Levan produced by Gluconobacter spp.has great potential in biotechnological applications.However,Gluconobacter spp.can synthesize organic acids during fermentation,resulting in environmental acidification.Few studies ... Levan produced by Gluconobacter spp.has great potential in biotechnological applications.However,Gluconobacter spp.can synthesize organic acids during fermentation,resulting in environmental acidification.Few studies have focused on the effects of environmental acidification on levan synthesis.This study revealed that the organic acids,mainly gluconic acid(GA)and 2-keto-gluconic acid(2KGA)secreted by Gluconobacter sp.MP2116 created a highly acidic environment(pH<3)that inhibited levan biosynthesis.The levansucrase derived from strain MP2116 had high enzyme activity at pH 4.0~pH 6.5.When the ambient pH was less than 3,the enzyme activity decreased by 67%.Knocking out the mgdh gene of membrane-bound glucose dehydrogenase(mGDH)in the GA and 2KGA synthesis pathway in strain MP2116 eliminated the inhibitory effect of high acid levels on levansucrase function.As a result,the levan yield increased from 7.4 g/l(wild-type)to 18.8 g/l(Δmgdh)during fermentation without pH control.This study provides a new strategy for improving levan production by preventing the inhibition of polysaccharide synthesis by environmental acidification. 展开更多
关键词 LEVAN levansucrase ACIDIFICATION Membrane-bound glucose dehydrogenase
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