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首页> 外文期刊>Applied and Environmental Microbiology >Cloning and constitutive expression of the N-acetylneuraminate lyase gene of Escherichia coli.
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Cloning and constitutive expression of the N-acetylneuraminate lyase gene of Escherichia coli.

机译:大肠杆菌N-乙酰神经氨酸裂解酶基因的克隆和组成性表达。

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The N-acetylneuraminate (NANA) lyase (EC 4.1.3.3) gene from Escherichia coli was self-cloned in E. coli. Transformants were selected by complementation of a NANA lyase-deficient E. coli strain. One clone was found to produce NANA lyase, and it contained a recombinant plasmid, pNAL1, with a 9.0-kilobase HindIII insert. The cloning of the NANA lyase gene resulted in the change from inducible to constitutive production of the enzyme. The level of expression of the NANA lyase gene in E. coli(pNAL1) clones was two- to three-fold higher than that in the fully induced wild-type strains.
机译:将来自大肠杆菌的N-乙酰神经氨酸(NANA)裂解酶(EC 4.1.3.3)基因克隆到大肠杆菌中。通过互补NANA裂解酶缺陷的大肠杆菌菌株来选择转化子。发现一个克隆产生NANA裂解酶,它包含一个重组质粒pNAL1,带有9.0碱基的HindIII插入片段。 NANA裂解酶基因的克隆导致了该酶从诱导型生产到组成型生产的转变。 NANA裂解酶基因在大肠杆菌(pNAL1)克隆中的表达水平比完全诱导的野生型菌株高2-3倍。

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