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91.
A Novel Class of Herbicides (Specific Inhibitors of Imidazoleglycerol Phosphate Dehydratase) 总被引:4,自引:2,他引:2
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Mori I Fonne-Pfister R Matsunaga S Tada S Kimura Y Iwasaki G Mano J Hatano M Nakano T Koizumi S Scheidegger A Hayakawa K Ohta D 《Plant physiology》1995,107(3):719-723
A new mode of herbicidal action was established by finding specific inhibitors of imidazoleglycerol phosphate dehydratase, an enzyme of histidine (His) biosynthesis. Three triazole phosphonates inhibited the reaction of the enzyme with Ki values of 40 [plus or minus] 6.5, 10 [plus or minus] 1.6, and 8.5 [plus or minus] 1.4 nM, respectively, and were highly cytotoxic to cultured plant cells. This effect was completely reversed by the addition of His, proving that the cytotoxicity was primarily caused by the inhibition of His biosynthesis. These inhibitors showed wide-spectrum, postemergent herbicidal activity at application rates ranging from 0.05 to 2 kg/ha. 相似文献
92.
93.
Naoko Sakihama Izumi Nishimura Shigehiro Obata Masateru Shin 《Photosynthesis research》1995,46(1-2):323-328
When 35%-acetone extract of spinach chloroplasts was separated by SDS-PAGE, ferredoxin-NADP reductase (FNR) appeared as a single band at a molecular mass of 35 kDa. After the polypeptides on the SDS-PAGE plate were electroblotted onto PVDF membrane, the FNR band was cut out and analyzed for N-terminal structure in a gas-phase protein sequencer. Two different FNR peptides were identified: one with glutamine at its N-terminus (Gln-FNR) and the other with -pyroglutamic acid (tFNR) fraction was extracted from chloroplasts with their loosely bound FNR (lFNR) fraction removed in advance. The tFNR fraction contained Gln-FNR only. The Gln-FNR could be highly purified by affinity chromatography using a ferredoxin column. The purified Gln-FNR was digested with arginyl endopeptidase for peptide mapping and partial sequence analysis. Primary structure of Gln-FNR differed from that of lFNR
loosely bound FNR
-
tFNR
tightly bound FNR
- -pyroglutamic acid at N-terminus 相似文献
94.
Masaru Nakano Keizo Hosokawa Tomo Oomiya Saburo Yamamura 《Plant Cell, Tissue and Organ Culture》1995,41(3):221-227
A protoplast-to-plant system was developed in Gentiana using a gellan gum-embedding culture. Viable protoplasts could be routinely isolated from in vitro-grown plantlets, and they were embedded in 0.2% gellan gum-solidified B5 medium containing 2 mg l-1 NAA, 0.1 mg l-1 TDZ, 0.1 M sucrose and 0.4 M mannitol. Weekly addition of fresh liquid medium was essential for preventing cell browning. Colony growth was promoted by lowering mannitol concentration of the culture media after one month, and visible colonies were produced after 2 months of culture. Shoot regeneration from protoplast-derived calluses was stimulated by 1 to 10 mg l-1 TDZ in combination with 0.1 mg l-1 NAA. Protoplast-derived plants were recovered following rooting of the shoots in plant growth regulator-free medium and they were successfully transferred to soil.Abbreviations BA
benzylaminopurine
- FDA
fluorescein diacetate
- FW
fresh weight
- MES
2-N-morpholinoethane sulfonic acid
- NAA
-naphthaleneacetic acid
- TDZ
N-1,2,3-thiadiazol-5-yl-N-phenylurea (also called thidiazuron) 相似文献
95.
96.
97.
T. Ito Naoko Udaka Yoshiaki Inayama Hitoshi Kitamura Masayoshi Kanisawa 《Histochemistry and cell biology》1997,109(1):67-73
We have examined the distribution of calcium-binding proteins (CaBPs) in adult and fetal lungs of Syrian golden hamsters
(Mesocricetus auratus) using immunostaining with confocal laser microscopy and electron microscopy. Single and grouped (neuroepithelial body; NEB)
endocrine cells were distributed from bronchi to alveolar ducts in the adult lung. Serial frozen sections immunostained for
CaBPs in combination with immunostaining for endocrine markers such as calcitonin gene-related peptide, serotonin, PGP9.5,
and synaptophysin revealed that positive immunostaining for calbindin-D28K (CB-D28K) was seen in single endocrine cells and NEBs. However, other so-called EF-hand family CaBPs, parvalbumin and calretinin,
were not detected. Electron microscopically, positive immunoreaction for CB-D28K was mainly in the organelle-free cytoplasmic
matrix of endocrine cells, and partly in nuclei and associated with secretory granules and endoplasmic reticulum. In fetal
developing lungs, endocrine cells appeared first on gestational day 13, and they were positive for all the endocrine markers
used. However, pulmonary endocrine cells were positively immunostained for CB-D28K from gestational days 15 and 16 onward.
In summary, our observations suggest that CB-D28K is a useful marker for endocrine cells of the lung, and CB-D28K could function
as a mediator of endocrine stimulation or calcium homeostasis in pulmonary endocrine cells.
Accepted: 17 June 1997 相似文献
98.
Immunocytochemical localization of thrombomodulin in the aqueous humor passage of the rat eye 总被引:1,自引:1,他引:0
T. Daimon Mutsuyoshi Kazama Yukari Miyajima Masahiko Nakano 《Histochemistry and cell biology》1997,108(2):121-131
This report describes the distribution and localization of thrombomodulin (TM) in the rat eye by light and electron microscopic
immunocytochemistry. In addition to the endothelium of the entire vasculature, TM was found on the non-vascular structures
lining the cavities of the posterior and anterior chambers and the limbus. TM was localized on the basal, lateral, and apical
plasma membranes of the inner and outer ciliary epithelium, and the posterior iris epithelium in which there was no polarized
expression of TM. In the anterior chamber, TM was localized on the luminal surface of the corneal endothelium, but was negative
on the anterior border layer of the iris, which is composed of a discontinuous layer of fibroblasts and collagen fibers. Thus,
TM was present at sites of cell-to-cell contact. TM was also present on the endothelia of the trabecular meshwork and the
Schlemm’s canal in the limbus. TM was localized not only on the luminal plasma membrane, but also on the cytoplasmic giant
vacuoles in the endothelial cells of the Schlemm’s canal. These findings extend the importance of anticoagulant mechanisms
to the systems of secretion, circulation, and drainage of the aqueous humor.
Accepted: 18 March 1997 相似文献
99.
Koichiro Suzuki Kenji Kanazawa Kyoko Higuchi Naoko K. Nishizawa Satoshi Mori 《Biometals》1997,10(2):77-84
In a previous paper we reported that an acidic 36 kDa peptide is the most strongly induced peptide among several peptides induced by Fe deficiency in barley roots. In this paper, polyclonal antibodies were raised against the 36 kDa peptide. This peptide appeared in the roots of all the graminaceous species tested (barley, rye, wheat, oat, maize, sorghum and rice) in response to Fe deficiency. More of the peptide was found in the roots of graminaceous species which secrete higher amounts of mugineic acids (MAs) under Fe deficient nutrition status. Induction of the 36 kDa peptide was first observed on the third day of Fe deficiency, rising to a maximum value on the seventh day. The trend has a positive correlation with secretion of MAs during Fe deficiency. Further, resupply of Fe resulted in a decrease in peptide production on the second day, reaching a control level on the seventh day. The rate of decrease in peptide production was observed to be slower than that of MA secretion. Other nutrient stresses such as B excess, B deficiency, Cu excess, Cu deficiency, Mn excess, Mn deficiency, Zn excess and Zn deficiency induced far less of the peptide. The specific expression of the 36 kDa peptide in roots of graminaceous species under Fe deficiency suggested the positive association of the peptide with a specific Fe deficiency tolerance mechanism in graminaceous plants. 相似文献
100.
Minoru Yonezawa Masahiro Takahata Naoko Banzawa Nobuyuki Matsubara Yasuo Watanabe Hirokazu Narita 《Microbiology and immunology》1995,39(4):243-247
Artificial mutations of Gyrase A protein (GyrA) in Escherichia coli by site-directed mutagenesis were generated to analyze quinolone-resistant mechanisms. By genetic analysis of gyrA genes in a gyrA temperature sensitive (Ts) background, exchange of Ser at the NH2-terminal 83rd position of GyrA to Trp, Leu, Phe, Tyr, Ala, Val, and Ile caused bacterial resistance to the quinolones, while exchange to Gly, Asn, Lys, Arg and Asp did not confer resistance. These results indicate that it is the most important for the 83rd amino acid residue to be hydrophobic in expressing the phenotype of resistance to the quinolones. These findings also suggest that the hydroxyl group of Ser would not play a major role in the quinolone-gyrase interaction and Ser83 would not interact directly with other amino acid residues. 相似文献