Highly Efficient Leaf Base Protoplast Isolation and Transient Expression Systems for Orchids and Other Important Monocot Crops
Versatile protoplast platforms greatly facilitate the development of modern botany. However, efficient protoplast-based systems are still challenging for numerous horticultural plants and crops. Orchids are globally cultivated ornamental and medicinal monocot plants, but few efficient protoplast iso...
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Published in | Frontiers in plant science Vol. 12; p. 626015 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
15.02.2021
|
Subjects | |
Online Access | Get full text |
ISSN | 1664-462X 1664-462X |
DOI | 10.3389/fpls.2021.626015 |
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Summary: | Versatile protoplast platforms greatly facilitate the development of modern botany. However, efficient protoplast-based systems are still challenging for numerous horticultural plants and crops. Orchids are globally cultivated ornamental and medicinal monocot plants, but few efficient protoplast isolation and transient expression systems have been developed. In this study, we established a highly efficient orchid protoplast isolation protocol by selecting suitable source materials and optimizing the enzymatic conditions, which required optimal D-mannitol concentrations (0.4–0.6 M) combined with optimal 1.2% cellulose and 0.6% macerozyme, 5 μM of 2-mercaptoethanol and 6 h digestion. Tissue- and organ-specific protoplasts were successfully isolated from young leaves [∼3.22 × 10
6
/g fresh weight (FW)], flower pedicels (∼5.26 × 10
6
/g FW), and young root tips (∼7.66 × 10
5
/g FW) of
Cymbidium
orchids. This protocol recommends the leaf base tissues (the tender part of young leaves attached to the stem) as better source materials. High yielding viable protoplasts were isolated from the leaf base of
Cymbidium
(∼2.50 × 10
7
/g FW),
Phalaenopsis
(1.83 × 10
7
/g FW),
Paphiopedilum
(1.10 × 10
7
/g FW),
Dendrobium
(8.21 × 10
6
/g FW),
Arundina
(3.78 × 10
6
/g FW) orchids, and other economically important monocot crops including maize (
Zea mays
) (3.25 × 10
7
/g FW) and rice (
Oryza sativa
) (4.31 × 10
7
/g FW), which showed marked advantages over previous mesophyll protoplast isolation protocols. Leaf base protoplasts of
Cymbidium
orchids were used for polyethylene glycol (PEG)-mediated transfection, and a transfection efficiency of more than 80% was achieved. This leaf base protoplast system was applied successfully to analyze the
CsDELLA
-mediated gibberellin signaling in
Cymbidium
orchids. We investigated the subcellular localization of the CsDELLA-green fluorescent protein fusion and analyzed the role of
CsDELLA
in the regulation of gibberellin to flowering-related genes via efficient transient overexpression and gene silencing of
CsDELLA
in
Cymbidium
protoplasts. This protoplast isolation and transient expression system is the most efficient based on the documented results to date. It can be widely used for cellular and molecular studies in orchids and other economically important monocot crops, especially for those lacking an efficient genetic transformation system
in vivo
. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Vladimir Orbovic, University of Florida, United States Reviewed by: Hong-Hwa Chen, National Cheng Kung University, Taiwan; Ali Parsaeimehr, Delaware State University, United States This article was submitted to Technical Advances in Plant Science, a section of the journal Frontiers in Plant Science |
ISSN: | 1664-462X 1664-462X |
DOI: | 10.3389/fpls.2021.626015 |