期刊
BIOCELL
卷 46, 期 9, 页码 2123-2131出版社
TECH SCIENCE PRESS
DOI: 10.32604/biocell.2022.020229
关键词
NbNAC1 transcription factor; Nicotiana benthamiana; Prokaryotic expression; Purification; Antibodies
类别
资金
- National Natural Science Foundation of China [31500209]
- Natural Science Foundation of Jiangsu Province of China [BK20201431]
- Agricultural science and technology independent innovation Foundation of Jiangsu Province of China [CX (20) 3128]
- Open Project Program of Joint International Research Laboratory of Agriculture
- Ministry of Education of China, Yangzhou University [JILARKF202006]
- Qing Lan Project of Yangzhou University
- Yangzhou University of High-end Talent Support Program
The NAC superfamily is a large plant-specific family of transcription factors, and recent studies have shown that NAC1 plays an important role in plant response to biotic and abiotic stimuli. In this study, researchers focused on developing a prokaryotic expression system to produce the NbNAC1 protein in Escherichia coli and preparing its polyclonal antibody. They successfully expressed and purified the NbNAC1 protein using two different expression vectors, and chose the His-tagged NbNAC1 protein for immunization to generate a highly specific anti-NbNAC1 polyclonal antibody.
The NAC (NAM, ATAF, and CUC) superfamily is one of the largest plant-specific families containing transcription factors. An increasing number of studies suggest that NAC1 is involved in plants response to different biotic and abiotic stimulis. Nicotiana benthamiana is a widely used system for evaluating plant-pathogen interactions. In order to study the biochemical function of NbNAC1, NbNAC1 protein and antibody are essential. Therefore, we focused on developing a prokaryotic expression system for producing the Nicotiana benthamiana NbNAC1 protein of in Escherichia coli and the preparation of its polyclonal antibody. Firstly, we constructed two different molecular weight prokaryotic expression vectors: pGE vector with GST tag (pGEX4T-1-NbNAC1) and pET expression vector with His tag (pET28a-NbNAC1). The NbNAC1 protein can be successfully expressed in both vectors. The His-tagged NbNAC1 proteins are insoluble, while the GST-tagged NbNAC1 proteins are partially soluble. We then successfully purified and enriched both proteins. The His-tagged NbNAC1 was chosen to immunize rabbits owing to an unknown protein accompanying the GST-tagged NbNAC1. The anti-NbNAC1 polyclonal antibody had good specificity and could be used in subsequent protein-related studies.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据