TY - CHAP
T1 - Isolation and Regeneration of Wheat Mesophyll Protoplasts: Using a Short Protocol
AU - Dedicova, Beata
AU - Olsson, Niklas
AU - Ivarson, Emelie
AU - Hofvander, Per
PY - 2025
Y1 - 2025
N2 - Plant protoplasts serve as valuable tools for studying the fundamental properties and functions of cells. For example, protoplasts have been used to analyze cell organelles, the cell cycle, and cell wall deposition. Another application involves protoplast fusion to create somaclonal hybrids and facilitate genetic modifications. Additionally, plant protoplasts are successfully utilized in experiments aimed at mitigating heavy metal toxicity, plant stress, and perception responses, as well as robust expression screening systems for recalcitrant species. Protoplasts from various plant species have become essential in genome editing technologies, with their application established in numerous laboratories today. Here, we present a reproducible and concise method for isolating wheat mesophyll protoplasts from two spring varieties, Canon and Alderon, derived from in vitro seedlings. A cell counter and fluorescent staining were employed to determine the concentration and viability of freshly isolated wheat protoplasts. A modified culture medium initiated the first cell divisions of one wheat genotype within 8 days after the protoplasts were placed in the culture.
AB - Plant protoplasts serve as valuable tools for studying the fundamental properties and functions of cells. For example, protoplasts have been used to analyze cell organelles, the cell cycle, and cell wall deposition. Another application involves protoplast fusion to create somaclonal hybrids and facilitate genetic modifications. Additionally, plant protoplasts are successfully utilized in experiments aimed at mitigating heavy metal toxicity, plant stress, and perception responses, as well as robust expression screening systems for recalcitrant species. Protoplasts from various plant species have become essential in genome editing technologies, with their application established in numerous laboratories today. Here, we present a reproducible and concise method for isolating wheat mesophyll protoplasts from two spring varieties, Canon and Alderon, derived from in vitro seedlings. A cell counter and fluorescent staining were employed to determine the concentration and viability of freshly isolated wheat protoplasts. A modified culture medium initiated the first cell divisions of one wheat genotype within 8 days after the protoplasts were placed in the culture.
UR - https://res.slu.se/id/publ/720dbc89-f571-4f46-a0f7-c964942b1d1f
U2 - 10.5772/intechopen.1012268
DO - 10.5772/intechopen.1012268
M3 - Book chapter
SN - 978-1-83635-650-9
SN - 978-1-83635-649-3
VL - 71
T3 - Biochemistry
BT - Cell Culture Technologies – Primary Cell Isolation, Growth and Analysi
PB - Intech Open
ER -