• 한국환경과학회지
• /
• 제15권12호
• /
• pp.1109-1117
• /
• 2006

To investigate the influence of the mesophyll cells on stomatal opening in response to white light, the segments of isolated epidermis were transferred on partly exposed mesophyll cells of a leaf and stomatal apertures were measured. Transferring the isolated epidermis on partly exposed mesophyll cells of a leaf caused a marked increase on stomatal apertures while stomata in isolated epidermis incubated in MES buffer hardly opened. Mesophyll infiltration with photosynthetic inhibitors (DCMU, DCCD, $NaN_3$) was performed to elucidate the correlation between stomatal apertures and the degree of photosynthetic activity. It was found that transferring the isolated epidermis on partly exposed mesophyll cells of a leaf caused an increase of stomatal apertures depending on the degree of photosynthetic activities. In $NaN_3$ infiltrated leaf discs, transferring the fresh isolated epidermis on partly exposed mesophyll cells of a leaf showed no significant effect, but a slight increase on stomatal apertures. Isolated epidermis alone did not respond to the light properly, but if it was closely contacted with mesophyil cells, the stomata regained the ability of the light response. Therefore, it could be suggested that stomatai apertures were related with the degree of photosynthetic activity in the mesophyll cells.

• 한국환경과학회지
• /
• 제17권2호
• /
• pp.163-170
• /
• 2008

Protoplasts of Panax ginseng C. A. Meyer and Aralia continentalis K. (Araliaceae) were isolated from callus cells and mesophyll cells, respectively. The maximum yield of protoplasts isolated from callus cells of P. ginseng were obtained by incubation for 3 hrs in the enzyme mixture of 0.5% macerozyme, 1.5% cellulase, and 0.5 M mannitol as an osmoticum. In the case of mesophyll cells of A. continentalis, the highest yield of protoplasts were obtained by incubation for 5 hrs in the enzyme mixture of 1% macerozyme, 2% cellulase, and 0.6 M mannitol. A polyethylene glycol (PEG) treatment induced an intergeneric fusion of the protoplasts. The fusion products, that is, heterokaryocytes were obtained by treatment of 50% PEG containing 0.05 M Ca salts.

• Journal of Plant Biology
• /
• 제39권2호
• /
• pp.99-105
• /
• 1996

Immunocytochemistry utilizes the specificity of the antigen-antibody reaction to localize specific antigens in cells or cellular organelles. Here we report the use of monoclonal antibodies, in conjunction with gold-labeled second antibodies to study the ultrastructural localization and tissue distribution of the Mr 98, 000 anionic peroxidase and other wall antigens. The antibody specific for this wall peroxidase, mWP3, labeled mainly the cell wall area. At the tissue level, the Mr 98, 000 peroxidase is located predominantly in the leaf mesophyll, internal coleoptile and sieve elements, but not in the root, as assayed with these procedures. The coleoptile walls were less heavily stained than the walls of leaf mesophyll cells. At the subcellular level, it is localized mainly in intercellular regions of the cell walls. A similar staining pattern was revealed by mWP19, one of anti-$\beta$ glucosidase antibody, though it looked less heavily stained than one with mWP3. In order to serve as a control wall staining using IgM monoclonal antibodies, mWP18 was used. Most of the label is localized over wall regions of cells of the young leaf mesophyll and coleoptile.

• 한국전자현미경학회:학술대회논문집
• /
• 한국현미경학회 2001년도 제32차 춘계학술대회
• /
• pp.25-25
• /
• 2001

• 환경생물
• /
• 제23권3호
• /
• pp.221-227
• /
• 2005

The effects of light and $CO_2$ on the electrophysiological characteristics of guard cells in the intact leaf and isolated epidermis have been investigated. Fast hyperpolarization of guard cell apoplastic PD in the intact leaf was recorded reaching up to around 7 mV and 20 mV in response to light and $CO_2$. Whenever the experiments were attempted with isolated epidermis, there was no response to light and $CO_2$. In order to determine the influence of the mesophyll cells, the apoplastic PD of guard cells in isolated epidermis was measured in the presence of the mesophyll supernatant or the control medium. The apoplastic PD in isolated epidermis was hyperpolarized to -7mV, changing from -22mV to -29mV at 40 min. But, when isolated epidermis was incubated with the supernatant from mesophyll cells incubated in the light, the apoplastic PD in isolated epidermis was hyperpolarized to -19 mV, changing from -22 mV to -40.5 mV. $CO_2$ also caused a change of 0.1 to 0.3 pH unit in the intact leaf. However, this change was absent in isolated epidermis. A vibrating probe was used to detect the change in electrical currents at the surface of excised intact leaves and isolated epidermis. The reading of excised intact leaves in the dark was $0.5\muA\;cm^{-2},$ remaining steady until illuminated. Light increased the current on the surface of excised leaves to about $0.8\muA\;cm^{-2},$. However, light had no effect in the current on the surface of isolated epidermis. Apoplastic pH changes across the stomatal complex in response to light and dark were measured both in the intact leaves and isolated epidermis over the same time period using pH micro-electrodes. The guard cell wall of intact leaf was acidified to 2.5 pH unit, falling from pH 7.5 to pH 5.0 in the first 10 min. in the light. At the same time the guard cell wall pH of isolated epidermis fell from pH 7.5 to pH 7.0 at 10 min. The guard cell wall pH of isolated epidermis incubated in the mesophyll supernatant fell from pH 7.6 to pH 6.7 at 10 min. Likewise, It could be imagined that an electrical signal, chemicals and hormones propagated from the mesophyll in response to light and $CO_2$ could control a fast stomatal response.

• 생명과학회지
• /
• 제7권4호
• /
• pp.282-288
• /
• 1997

To obtain a basic information on the development of Genus Viola, ultrastructure and electrofusion process between the two protoplasts from wild Viola callus cells and pansy mesophyll cells were observed with a scanning electron microscopy(SEM) and transmission electron microscopy(TEM). In the ultrastructural observation of wild viola callus protoplasts and pansy mesophyll protoplasts using SEM, their cell walls were removed completely. A knob-like formation was observed on the enlarge surface of viola callus protoplasts. On the surface of pansy mesophyll protoplasts net-like chloroplasts were observed. In SEM observation of pansy mesophyll protoplasts, chloroplasts devoid of membrane were observed on the surface the protoplasts. Pearl chain was formed by applying AC field of 200 V/cm at 1.0 MHz for 43 sec. The lysis of plasma membranes and fusion process occurred by applying a 1,600 V/cm DC pulse twice for 1 sec. After 1-2 hours of a DC pulse application, it was observed that the two protoplasts were fused completely into one cell. In TEM observation of the fused cell, many small vacuoles were located in the fusion area of the two protoplasts. Indeed, two distinct regions were observed during fusing process; in one region, a nucleus was found, while in the other region, both nucleus and nucleous were found.

• 한국식물학회:학술대회논문집
• /
• 한국식물학회 1993년도 제7회 식물생명공학 심포지움 식물 세포 분화의 분자적 접근 Seventh Symposium on Plant Biotechnology -Approach to Plant Cell Differentiation-
• /
• pp.149-155
• /
• 1993

• KSBB Journal
• /
• 제5권1호
• /
• pp.43-47
• /
• 1990

약난초는 내장산 이남에서만 자생하는 상록성 난으로 관상용 뿐 아니라 점질이 높은 구경은 약용(점활제)으로써 이용가치가 높은 중요한 자원식물중의 하나이다. 본 연구에서는 이와같은 약난초의 다량증식을 위하여 몇 가지 실험을 하여 다음과 같은 결과를 었다. Green pod를 이용하여 미숙종자를 개체로 유도시키는 것은 그 유도율이 낮았고 생장점을 이용, 캘러스를 유도하여 PLB를 형성시켜 개체로 유도하는 것이 용이하였다. 그러나 미숙종자의 이용도 배지조건등의 개량으로 가능하리라 사료된다. 캘러스의 형성은 Hyponex배지에 2.4-D(2mg/l)와 Kinetin(1mg/l)을 첨가하였을 때 높았다. 한편 업육조직 및 배양세포로부터 분리시킨 원형질체는 70%이상의 생존력을 나타내었고 형광현미경 관찰을 통하여 세포벽의 재생을 확인하였다. 이와 같은 실험결과는 자생란의 다량증식 뿐 아니라 잡종난 식물체를 유도하는 제반 실험에 응용될 수 있는 기초 자료가 될 수 있으리라 사료된다.

• The Plant Pathology Journal
• /
• 제31권3호
• /
• pp.299-304
• /
• 2015

Interaction of the the rust fungus Puccinia miscanthi with the biofuel plant Miscanthus sinensis during the teliospore phase was investigated by light and electron microscopy. P. miscanthi telia were oval-shaped and present on both the adaxial and abaxial leaf surfaces. Teliospores were brown, one-septate (two-celled), and had pedicels attached to one end. Transmission electron microscopy revealed numerous electron-translucent lipid globules in the cytoplasm of teliospores. Extensive cell wall dissolution around hyphae was not observed in the host tissues beneath the telia. Hyphae were found between mesophyll cells in the leaf tissues as well as in host cells. Intracellular hyphae, possibly haustoria, possessed electron-dense fungal cell walls encased by an electron-transparent fibrillar extrahaustorial sheath that had an electron-dense extrahaustorial membrane. The infected host cells appeared to maintain their membrane-bound structures such as nuclei and chloroplasts. These results suggest that the rust fungus maintains its biotrophic phase with most mesophyll cells of M. sinensis. Such a nutritional mode would permit the rust fungus to obtain food reserves for transient growth in the course of host alteration.

• Journal of Plant Biotechnology
• /
• 제34권3호
• /
• pp.271-275
• /
• 2007

엽록체 형질전환된 식물체를 얻으려면 먼저 세포수준에서 모든 엽록체가 형질전환되어야 하는데, 세포내에는 많은 수의 엽록체가 존재하므로, 엽록체 형질전환 벡터가 전이되어 형질전환된 엽록체는 선발배지에서 선택적으로 분열을 계속하고 형질전환되지 않은 엽록체들은 분열을 하지 못하게 되어, 결국 해당 세포내의 모든 엽록체가 형질전환된 상태에 이르게 된다. 따라서 만일 해당 세포내에 엽록체의 수가 적으면 그만큼 효율적으로 엽록체 형질전환을 할 수 있을 것이다. 본 연구에서는 담배의 FtsZ 유전자를 핵형질전환법으로 과잉 발현시킴으로써 엽록체의 분열이 저해되어 엽육세포내에 거대한 엽록체 3-5개를 가진 담배식물체의 엽육조직을 이용하여, 엽록체 형질전환을 한 결과, 엽록체 형질전환 빈도가 약 40% 증가되었다.