Co-expression of nitrogenase proteins in cotton (Gossypium hirsutum L.).

Chemical nitrogen fertilizer can maintain crop productivity, but overuse of chemical nitrogen fertilizers leads to economic costs and environmental pollution. One approach to reduce use of nitrogen fertilizers is to transfer nitrogenase biosynthetic pathway to non-legume plants. Fe protein encoded b...

Full description

Saved in:
Bibliographic Details
Main Authors: Yimin Shang, Wenfang Guo, Xiaomeng Liu, Lei Ma, Dehu Liu, Sanfeng Chen
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2023-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0290556
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1846129491736264704
author Yimin Shang
Wenfang Guo
Xiaomeng Liu
Lei Ma
Dehu Liu
Sanfeng Chen
author_facet Yimin Shang
Wenfang Guo
Xiaomeng Liu
Lei Ma
Dehu Liu
Sanfeng Chen
author_sort Yimin Shang
collection DOAJ
description Chemical nitrogen fertilizer can maintain crop productivity, but overuse of chemical nitrogen fertilizers leads to economic costs and environmental pollution. One approach to reduce use of nitrogen fertilizers is to transfer nitrogenase biosynthetic pathway to non-legume plants. Fe protein encoded by nifH and MoFe protein encoded by nifD and nifK are two structural components of nitrogenase. NifB encoded by nifB is a critical maturase that catalyzes the first committed step in the biosynthesis of nitrogenase FeMo-cofactor that binds and reduces N2. Expression of the nifB, nifH, nifD and nifK is essential to generate plants that are able to fix atmospheric N2. In this study, the four genes (nifB, nifH, nifD and nifK) from Paenibacillu polymyxaWLY78 were assembled in plant expression vector pCAMBIA1301 via Cre/LoxP recombination system, yielding the recombinant expression vector pCAMBIA1301-nifBHDK. Then, the four nif genes carried in the expression vector were co-introduced into upland cotton R15 using Agrobacterium tumefaciens-mediated transformation. Homozygous transgenic cotton lines B2, B5 and B17 of T3 generation were selected by PCR and RT-PCR. qRT-PCR showed that nifB, nifH, nifD and nifK were co-expressed in the transgenic cottons at similar levels. Western blotting analysis demonstrated that NifB, NifH, NifD and NifK were co-produced in the transgenic cottons. Co-expression of the four critical Nif proteins (NifB, NifH, NifD and NifK) in cottons represents an important step in engineering nitrogenase biosynthetic pathway to non-legume plants.
format Article
id doaj-art-c041b5c08ee54e0f9c2816c58969c71b
institution Kabale University
issn 1932-6203
language English
publishDate 2023-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj-art-c041b5c08ee54e0f9c2816c58969c71b2024-12-10T05:31:53ZengPublic Library of Science (PLoS)PLoS ONE1932-62032023-01-01188e029055610.1371/journal.pone.0290556Co-expression of nitrogenase proteins in cotton (Gossypium hirsutum L.).Yimin ShangWenfang GuoXiaomeng LiuLei MaDehu LiuSanfeng ChenChemical nitrogen fertilizer can maintain crop productivity, but overuse of chemical nitrogen fertilizers leads to economic costs and environmental pollution. One approach to reduce use of nitrogen fertilizers is to transfer nitrogenase biosynthetic pathway to non-legume plants. Fe protein encoded by nifH and MoFe protein encoded by nifD and nifK are two structural components of nitrogenase. NifB encoded by nifB is a critical maturase that catalyzes the first committed step in the biosynthesis of nitrogenase FeMo-cofactor that binds and reduces N2. Expression of the nifB, nifH, nifD and nifK is essential to generate plants that are able to fix atmospheric N2. In this study, the four genes (nifB, nifH, nifD and nifK) from Paenibacillu polymyxaWLY78 were assembled in plant expression vector pCAMBIA1301 via Cre/LoxP recombination system, yielding the recombinant expression vector pCAMBIA1301-nifBHDK. Then, the four nif genes carried in the expression vector were co-introduced into upland cotton R15 using Agrobacterium tumefaciens-mediated transformation. Homozygous transgenic cotton lines B2, B5 and B17 of T3 generation were selected by PCR and RT-PCR. qRT-PCR showed that nifB, nifH, nifD and nifK were co-expressed in the transgenic cottons at similar levels. Western blotting analysis demonstrated that NifB, NifH, NifD and NifK were co-produced in the transgenic cottons. Co-expression of the four critical Nif proteins (NifB, NifH, NifD and NifK) in cottons represents an important step in engineering nitrogenase biosynthetic pathway to non-legume plants.https://doi.org/10.1371/journal.pone.0290556
spellingShingle Yimin Shang
Wenfang Guo
Xiaomeng Liu
Lei Ma
Dehu Liu
Sanfeng Chen
Co-expression of nitrogenase proteins in cotton (Gossypium hirsutum L.).
PLoS ONE
title Co-expression of nitrogenase proteins in cotton (Gossypium hirsutum L.).
title_full Co-expression of nitrogenase proteins in cotton (Gossypium hirsutum L.).
title_fullStr Co-expression of nitrogenase proteins in cotton (Gossypium hirsutum L.).
title_full_unstemmed Co-expression of nitrogenase proteins in cotton (Gossypium hirsutum L.).
title_short Co-expression of nitrogenase proteins in cotton (Gossypium hirsutum L.).
title_sort co expression of nitrogenase proteins in cotton gossypium hirsutum l
url https://doi.org/10.1371/journal.pone.0290556
work_keys_str_mv AT yiminshang coexpressionofnitrogenaseproteinsincottongossypiumhirsutuml
AT wenfangguo coexpressionofnitrogenaseproteinsincottongossypiumhirsutuml
AT xiaomengliu coexpressionofnitrogenaseproteinsincottongossypiumhirsutuml
AT leima coexpressionofnitrogenaseproteinsincottongossypiumhirsutuml
AT dehuliu coexpressionofnitrogenaseproteinsincottongossypiumhirsutuml
AT sanfengchen coexpressionofnitrogenaseproteinsincottongossypiumhirsutuml