Combined Assembly and Targeted Integration of Multigene for Nitrogenase Biosynthetic Pathway in .

ACS Synth Biol

State Key Laboratory for Agrobiotechnology, College of Biological Sciences and Key Laboratory of Soil Microbiology of Agriculture Ministry , China Agricultural University, Beijing , P. R. China.

Published: August 2019

Biological nitrogen fixation, a process unique to diazotrophic prokaryote, is catalyzed by the nitrogenase complex. There has been a long-standing interest in reconstituting a nitrogenase biosynthetic pathway in a eukaryotic host with the final aim of developing N-fixing cereal crops. In this study, we report that a nitrogenase biosynthetic pathway (∼38 kb containing 15 genes) was assembled in two individual one-step methods via assembly and integrated at δ and sites in chromosome. Of the 15 genes, 11 genes (, , , , , , , , , , ) were from WLY78 and 4 genes (, , , ) were from The 15-gene nitrogenase biosynthetic pathway was correctly assembled and transcribed in the recombinant The NifDK tetramer with an identical molecular weight as that of was formed in yeast and the expressed NifH exhibited the activity of Fe protein. This study demonstrates that it will be possible to produce active nitrogenase in eukaryotic hosts.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acssynbio.9b00060DOI Listing

Publication Analysis

Top Keywords

nitrogenase biosynthetic
16
biosynthetic pathway
16
nitrogenase
6
combined assembly
4
assembly targeted
4
targeted integration
4
integration multigene
4
multigene nitrogenase
4
biosynthetic
4
pathway
4

Similar Publications

GmbZIP4a/b Positively Regulate Nodule Number by Affecting Cytokinin Biosynthesis in .

Int J Mol Sci

December 2024

Guangdong Provincial Key Laboratory of Plant Adaptation and Molecular Design, Innovative Center of Molecular Genetics and Evolution, School of Life Sciences, Guangzhou University, Guangzhou 510006, China.

Legumes have the capability to form nodules that facilitate symbiotic nitrogen fixation (SNF) with rhizobia. Given the substantial energy consumption during the process of SNF, legumes need to optimize nodule number in response to everchanging environmental scenarios. The TGACG BINDING FACTOR1/4 (TGA1/4) are key players in the basal immune response of plants.

View Article and Find Full Text PDF

The archaeal class is widely and abundantly distributed in anoxic habitats. Metagenomic studies have suggested that they are mixotrophic, capable of CO fixation and heterotrophic growth, and involved in acetogenesis and lignin degradation. We analyzed 35 metagenome-assembled genomes (MAGs), including the first complete circularized MAG (cMAG) of the Bathy-6 subgroup, from the metagenomes of three full-scale pulp and paper mill anaerobic digesters and three laboratory methanogenic enrichment cultures maintained on pre-treated poplar.

View Article and Find Full Text PDF

A microaerobically induced small heat shock protein contributes to / symbiosis and interacts with a wide range of bacteroid proteins.

Appl Environ Microbiol

December 2024

Centro de Biotecnología y Genómica de Plantas, Universidad Politécnica de Madrid - Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA/CSIC), Madrid, Spain.

During the establishment of the symbiosis with legume plants, rhizobia are exposed to hostile physical and chemical microenvironments to which adaptations are required. Stress response proteins including small heat shock proteins (sHSPs) were previously shown to be differentially regulated in bacteroids induced by bv. viciae UPM791 in different hosts.

View Article and Find Full Text PDF
Article Synopsis
  • This study explores the construction of synthetic phototrophic microbial consortia for sustainable bioenergy, highlighting the challenges in regulation and efficiency.
  • It successfully engineered a community utilizing specific strains, allowing for the production of biohydrogen and fatty acids while fixing nitrogen and carbon dioxide.
  • Key findings indicate that circadian illumination and infrared light enhance H and fatty acid production by regulating metabolic activities and protein expression related to nitrogen fixation and photosynthesis.
View Article and Find Full Text PDF

NifEN: a versatile player in nitrogenase assembly, catalysis and evolution.

J Biol Inorg Chem

December 2024

Department of Molecular Biology and Biochemistry, University of California, Irvine, CA, 92697-3900, USA.

The Mo-nitrogenase catalyzes the reduction of N to NH at the cofactor of its catalytic NifDK component. NifEN shares considerable homology with NifDK in primary sequence, tertiary structure and associated metallocenters. Better known for its biosynthetic function to convert an all-iron precursor (L-cluster; [FeSC]) to a mature cofactor (M-cluster; [(R-homocitrate) MoFeSC]), NifEN also mimics NifDK in catalyzing substrate reduction at ambient conditions.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!