TY - JOUR
T1 - A novel microsurgery method for intact plant tissue at the single cell level using ArF excimer laser microprojection
AU - Kajiyama, Shin'ichiro
AU - Shoji, Takeshi
AU - Okuda, Shinya
AU - Izumi, Yoshihiro
AU - Fukusaki, Ei Ichiro
AU - Kobayashi, Akio
PY - 2006/2/5
Y1 - 2006/2/5
N2 - A novel microsurgery technique for the partial removal of rigid cell-walls in intact plant tissue is established. Using a size-variable slit, an ArF excimer laser was microprojected on the surface of the targeted cell, and this method enabled the area- and depth-controllable processing of the cortical structure of plant cells including the cuticle and cell wall layer. In epidermal cells of all tested plants, viabilities of more than 90% were retained 24 h after irradiation. Scanning electron microscope (SEM) observation revealed that the cuticle layer of the irradiated region was completely ablated, and the cellulose microfibrils of the secondary cell wall were partially removed; furthermore, 4 days after laser treatment, the regeneration of cell wall fibrils was observed. As a model experiment, the transient expression of synthetic green fluorescent protein (sGFP) was performed by the microinjection of cauliflower mosaic virus (CMV) 35S promoter-derived sGFP gene through an "aperture" in the treated cell surface. Moreover, micron-sized fluorescent beads were successfully introduced by the same method into the onion cells indicating that this method can be used to introduce foreign materials as large as organelles.
AB - A novel microsurgery technique for the partial removal of rigid cell-walls in intact plant tissue is established. Using a size-variable slit, an ArF excimer laser was microprojected on the surface of the targeted cell, and this method enabled the area- and depth-controllable processing of the cortical structure of plant cells including the cuticle and cell wall layer. In epidermal cells of all tested plants, viabilities of more than 90% were retained 24 h after irradiation. Scanning electron microscope (SEM) observation revealed that the cuticle layer of the irradiated region was completely ablated, and the cellulose microfibrils of the secondary cell wall were partially removed; furthermore, 4 days after laser treatment, the regeneration of cell wall fibrils was observed. As a model experiment, the transient expression of synthetic green fluorescent protein (sGFP) was performed by the microinjection of cauliflower mosaic virus (CMV) 35S promoter-derived sGFP gene through an "aperture" in the treated cell surface. Moreover, micron-sized fluorescent beads were successfully introduced by the same method into the onion cells indicating that this method can be used to introduce foreign materials as large as organelles.
UR - http://www.scopus.com/inward/record.url?scp=33645582357&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33645582357&partnerID=8YFLogxK
U2 - 10.1002/bit.20709
DO - 10.1002/bit.20709
M3 - Article
C2 - 16193516
AN - SCOPUS:33645582357
SN - 0006-3592
VL - 93
SP - 325
EP - 331
JO - Biotechnology and Bioengineering
JF - Biotechnology and Bioengineering
IS - 2
ER -