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棘白菌素 B 生物合成基因簇中宿主毒性 EcdB 转录因子蛋白的功能表征。

Functional characterization of host toxic EcdB transcription factor protein of echinocandin B biosynthetic gene cluster.

机构信息

Department of Biotechnology, Central University of South Bihar, Panchanpur, Gaya, India.

National Institute of Plant Genome Research, Aruna Asaf Ali Marg, New Delhi, India.

出版信息

Biotechnol Appl Biochem. 2019 Jul;66(4):626-633. doi: 10.1002/bab.1763. Epub 2019 Jul 10.

Abstract

The ecdB is a transcription factor, located in the echinocandin B biosynthetic gene cluster of Emericella rugulosa NRRL11440. Here, we validated the ecdB mRNA sequence for functional expression and to explore the role of EcdB protein in the echinocandin B regulation. The sequence alignment study revealed that the ecdB coding sequence was found 75 bp shorter than the reference mRNA sequence. This coding sequence encodes for EcdB protein and comprises three conserved domains; DNA binding domain (DBD), coiled-coil domain, and signature middle homology region. The full-length and DBD (truncated) DNA sequences were expressed in Escherichia coli BL21(DE3) under different tested conditions. The expression of EcdB protein was found to be toxic, which curbs the cell growth. In contrast to truncated protein (GST:EcdB1-54), the full-length (GST:EcdB) protein was expressed at very low titer and not detectable in SDS-PAGE under the varying isopropyl β-d-1-thiogalactopyranoside (IPTG), temperature, and media conditions. However, GST:EcdB1-54 was successfully purified under standard conditions (0.5 mM IPTG at 0.5OD) with 33 kDa expected size. The functionality of GST:EcdB1-54 was attained by electrophoretic mobility shift assay study as a clear band shifting showed with ecdA promoter. Taken together, we conclude that EcdB interacts with the ecdA promoter that reflected to require for echinocandin B regulation.

摘要

ecdB 是一种转录因子,位于 rugulosa NRRL11440 中棘白菌素 B 生物合成基因簇中。在这里,我们验证了 ecdB mRNA 序列的功能表达,并探索了 EcdB 蛋白在棘白菌素 B 调节中的作用。序列比对研究表明,ecdB 编码序列比参考 mRNA 序列短 75bp。该编码序列编码 EcdB 蛋白,包含三个保守结构域;DNA 结合域(DBD)、卷曲螺旋域和特征中间同源区。全长和 DBD(截断)DNA 序列在不同测试条件下在大肠杆菌 BL21(DE3)中表达。发现 EcdB 蛋白的表达具有毒性,会抑制细胞生长。与截断蛋白(GST:EcdB1-54)相比,全长(GST:EcdB)蛋白在变化的异丙基 β-d-1-硫代半乳糖吡喃糖苷(IPTG)、温度和培养基条件下以非常低的效价表达,并且在 SDS-PAGE 中不可检测。然而,GST:EcdB1-54 在标准条件(0.5mM IPTG 在 0.5OD 下)下成功纯化,预期大小为 33kDa。通过电泳迁移率变动分析研究获得了 GST:EcdB1-54 的功能,因为清楚地显示了与 ecdA 启动子的带迁移。综上所述,我们得出结论,EcdB 与 ecdA 启动子相互作用,这反映了对棘白菌素 B 调节的要求。

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