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首页> 外文期刊>Journal of Applied Phycology >A duplicated carbonic anhydrase 1 (DCA1) promoter mediates the nitrate reductase gene switch of Dunaliella salina
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A duplicated carbonic anhydrase 1 (DCA1) promoter mediates the nitrate reductase gene switch of Dunaliella salina

机译:重复的碳酸酐酶1(DCA1)启动子介导了杜氏盐藻的硝酸还原酶基因开关

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The unicellular Dunaliella salina, the most extremely halotolerant eukaryote, is able to survive in salt concentrations from 0.05 to 5 M NaCl, whose halotolerant property encouraged us to develop salt-inducible promoters for research on transgenic bioreactors. A duplicated carbonic anhydrase 1 (DCA1) promoter from D. salina has been identified to drive the inducible expression of the bar gene under the induction of different NaCl concentrations. The purpose of this study was to identify whether the DCA1 promoter could drive and modulate the expression of the nitrate reductase (NR) gene in NR-deficient mutants of D. salina. Here, the wild-type NR gene under the control of the DCA1 promoter was transformed into the NR-deficient mutant (J1) of D. salina by electroporation, and the complemented transformant T1-J1 was screened by nitrate, in which NR activity was restored up to 48% of the wild-type (WT) cells. Different from the natural NR gene switch in WT cells where NR activity disappeared in ammonium medium, NR activity was detected in the T1-J1 cells despite changes of the nitrogen sources. Furthermore, both the NR transcripts and NR activity were increased with rising NaCl concentration from 0.5 to 2.0 M in the T1-J1 cells but not in the WT cells. These findings strongly support that the DCA1 promoter not only drives the inducible expression of the NR gene effectively, but also mediates lost of the natural NR gene switch in D. salina.
机译:单细胞杜氏盐藻,最耐盐的真核生物,能够在0.05至5 M NaCl的盐浓度下生存,其盐耐特性鼓励我们开发用于盐诱导的启动子,用于转基因生物反应器的研究。已经鉴定出来自盐生小球藻的重复碳酸酐酶1(DCA1)启动子,以在不同NaCl浓度的诱导下驱动bar基因的可诱导表达。这项研究的目的是要确定DCA1启动子是否可以驱动和调节盐沼D. salina突变体中硝酸还原酶(NR)基因的表达。在这里,在DCA1启动子控制下的野生型NR基因通过电穿孔转化为盐藻的NR缺失突变体(J1),并用硝酸盐筛选了互补的转化体T1-J1,其中NR活性为恢复了多达48%的野生型(WT)细胞。与野生型细胞中的天然NR基因转换不同,在铵盐培养基中NR活性消失了,尽管氮源发生了变化,在T1-J1细胞中仍检测到了NR活性。此外,在T1-J1细胞中,随着NaCl浓度从0.5M增加到2.0M,NR转录物和NR活性均增加,而在WT细胞中则不。这些发现强烈支持DCA1启动子不仅有效地驱动NR基因的可诱导表达,而且介导了盐藻中天然NR基因开关的丢失。

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