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Cloning, Prokaryotic Expression and Functional Characterization of NifH Gene from the Associative Nitrogen-Fixing Bacteria Klebsiella Variicola DX120E.
Qin, Ying; Huang, Yu-Yan; Khan, Qaisar; Zhang, Kun-Kun; Guo, Dao-Jun; Yang, Li-Tao; Li, Yang-Rui; Xing, Yong-Xiu.
Afiliação
  • Qin Y; College of Agriculture, Guangxi University, Nanning, China.
  • Huang YY; College of Agriculture, Guangxi University, Nanning, China.
  • Khan Q; College of Agriculture, Guangxi University, Nanning, China.
  • Zhang KK; College of Agriculture, Guangxi University, Nanning, China.
  • Guo DJ; College of Life Sciences and Engineering, Hexi University, Zhangye, China.
  • Yang LT; College of Agriculture, Guangxi University, Nanning, China.
  • Li YR; Guangxi Key Laboratory of Sugarcane Genetic Improvement, Key Laboratory of Sugarcane Biotechnology and Genetic Improvement (Guangxi), Ministry of Agriculture and Rural Affairs, Sugarcane Research Institute of Guangxi Academy of Agricultural Sciences, Sugarcane Research Center of Chinese Academy of A
  • Xing YX; College of Agriculture, Guangxi University, Nanning, China.
Iran J Biotechnol ; 21(3): e3451, 2023 Jul.
Article em En | MEDLINE | ID: mdl-38344705
ABSTRACT

Background:

Biological nitrogen fixation (BNF) is a unique mechanism in which microorganisms utilize the nitrogenase enzyme to catalyze the conversion of atmospheric nitrogen (N2) to ammonia (NH3). Fe protein, encoded by the nifH gene, is an essential component of the nitrogenase in Klebsiella variicola DX120E. However, the function of this gene in regulating nitrogen fixing activity is still unclear.

Objectives:

The objective of this study was to reveal the function of nifH gene in associative nitrogen-fixing bacteria Klebsiella variicola DX120E and micro-sugarcane system by immunoassay and gene editing. Materials and

Methods:

In the current investigation, the nifH gene was cloned in a pET-30a (+) vector and expressed in Escherichia coli. The NifH protein was purified and used to immunize rabbit, and then the serum was collected and purified to obtain rabbit anti-NifH polyclonal antibodies. The CRISPR-Cas9 system was applied to produce nifH mutant strains, and the nitrogen-fixing enzyme activity, gene, and protein expression were analyzed.

Results:

Both in vitro and in vivo NifH proteins were detected by Western blotting, which were 43 and 32 kDa respectively. The expression of nifD and nifK genes was decreased, and nitrogenase activity was reduced in the nifH mutant strain.

Conclusion:

The nifH gene mutant weakened the nitrogenase activity by regulating the expression of Fe protein, which suggests a potential strategy to study the nitrogen fixation-related genes and the interactions between endophytic nitrogen-fixing bacteria and sugarcane.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Iran J Biotechnol Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Iran J Biotechnol Ano de publicação: 2023 Tipo de documento: Article