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An efficient protocol for perennial ryegrass mesophyll protoplast isolation and transformation, and its application on interaction study between LpNOL and LpNYC1.

Identifieur interne : 001528 ( Main/Exploration ); précédent : 001527; suivant : 001529

An efficient protocol for perennial ryegrass mesophyll protoplast isolation and transformation, and its application on interaction study between LpNOL and LpNYC1.

Auteurs : Guohui Yu [République populaire de Chine] ; Qiang Cheng [République populaire de Chine] ; Zheni Xie [République populaire de Chine] ; Bin Xu [République populaire de Chine] ; Bingru Huang [États-Unis] ; Bingyu Zhao [États-Unis]

Source :

RBID : pubmed:28592987

Abstract

BACKGROUND

Perennial ryegrass (

RESULTS

In this report, a highly efficient protoplast isolation (5.6 × 10

CONCLUSION

This efficient protoplast isolation and transformation protocol is sufficient for studies on protein subcellular localization and protein-protein interaction, and shall be suitable for many other molecular biology applications where the mesophyll protoplast system is desirable in perennial ryegrass.


DOI: 10.1186/s13007-017-0196-0
PubMed: 28592987
PubMed Central: PMC5460552


Affiliations:


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<b>BACKGROUND</b>
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<b>RESULTS</b>
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<p>In this report, a highly efficient protoplast isolation (5.6 × 10</p>
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<b>CONCLUSION</b>
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<p>This efficient protoplast isolation and transformation protocol is sufficient for studies on protein subcellular localization and protein-protein interaction, and shall be suitable for many other molecular biology applications where the mesophyll protoplast system is desirable in perennial ryegrass.</p>
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<Day>29</Day>
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<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Perennial ryegrass (
<i>Lolium perenne</i>
L.) is an important temperate grass used for turf and forage purposes. With the increasing accumulation of genomic and transcriptomic data of perennial ryegrass, an efficient protoplast and transient gene expression protocol is highly desirable for in vivo gene functional studies in its homologous system.</AbstractText>
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<sup>7</sup>
protoplasts per gram of leaf material) and transient expression (plasmid transformation efficiency at 55.2%) was developed and the detailed protocol presented. Using this protocol, the subcellular locations of two ryegrass proteins were visualized in chloroplasts and nuclei, respectively, and protein-protein interaction between two chlorophyll catabolic enzymes (LpNOL and LpNYC1) was recorded in its homologous system for the first time.</AbstractText>
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