首页> 外文OA文献 >Expression of the genes coding for the xylanase Xys1 and the cellulase Cel1 from the straw-decomposing Streptomyces halstedii JM8 cloned into the amino-acid producer Brevibacterium lactofermentum ATCC13869
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Expression of the genes coding for the xylanase Xys1 and the cellulase Cel1 from the straw-decomposing Streptomyces halstedii JM8 cloned into the amino-acid producer Brevibacterium lactofermentum ATCC13869

机译:分解为氨基酸生产者的短杆菌Streptomyces halstedii JM8中编码木聚糖酶Xys1和纤维素酶Cel1的基因的表达克隆到氨基酸生产者乳铁短杆菌ATCC13869中

摘要

The xylanase ( xysA) and the cellulase ( celA1) genes from Streptomyces halstedii JM8 were cloned into Escherichia coli/ Brevibacterium lactofermentum shuttle vectors and successfully expressed in both hosts when placed downstream from the kanamycin resistance promoter (Pkan) from Tn 5 but not when under the control of their own promoters. Xylanase was secreted into the culture media of B. lactofermentum by removal of the same leader peptide as is removed in S. halstedii. The main difference between the production of xylanase by Streptomyces and corynebacteria was the low level of processing of the mature extracellular xylanase by B. lactofermentum, probably due to the lack of protease activity in this microorganism.
机译:将哈氏链霉菌JM8的木聚糖酶(xysA)和纤维素酶(celA1)基因克隆到大肠杆菌/乳铁短杆菌穿梭载体中,并在两个宿主中成功表达,当它们位于Tn 5的卡那霉素抗性启动子(Pkan)的下游时,但不能在宿主中表达自己的发起人的控制。通过去除与在哈氏链球菌中去除的相同的前导肽,木聚糖酶被分泌到乳铁芽孢杆菌的培养基中。链霉菌和棒状杆菌产生木聚糖酶之间的主要区别是乳铁芽孢杆菌对成熟细胞外木聚糖酶的加工水平较低,这可能是由于该微生物缺乏蛋白酶活性所致。

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