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31.
Masahiro Fukaya Kenji Tayama Hajime Okumura Hiroshi Masai Takeshi Uozumi Teruhiko Beppu 《Bioscience, biotechnology, and biochemistry》2013,77(7):2091-2097
An improved method for transformation of derivative strains of A. aceti subsp. aceti No. 1023 with plasmid DNA has been developed. Addition of polyethylene glycol or dimethylsulfoxide increased the transformation efficiency by a factor of about ten. In the presence of PEG 4,000, various transformation conditions were examined. Cells were also made transformation competent by treatment with other divalent cations than Ca2+ . The pH of the buffer did not affect the efficiency significantly. The growth phase influenced the efficiency. Mutants showing high competence were derived by treatment with N-methyl-N′-nitro-N-nitrosoguanidine. By the improved method using the highly transformable mutants, a transformation efficiency of approximately 105 transformants per γg plasmid DNA was achieved. 相似文献
32.
Mauseth James D. Uozumi Yoriko Plemons Brandon J. Landrum James V. 《Journal of plant research》1995,108(4):517-526
Wide-band tracheids are a specialized tracheid type in which an annular or helical secondary wall projects deeply into the
cell lumen. They are short, wide and spindle-shaped, and their bandlike secondary walls cover little of the primary wall,
leaving most of it available for water diffusion. Wide-band tracheids appear to store and conduct water while preventing the
spread of embolisms. They may be the most abundant tracheary element in the xylem, but they are always accompanied by at least
a few vessels. Typically, fibers are absent wherever wide-band tracheids are present. Wide-band tracheids occur in the primary
and secondary xylem of succulent stems, leaves and roots in genera of all three subfamilies of Cactaceae but were not found
in the relictual genusPereskia, which lacks succulent tissues. In the large subfamily Cactoideae, wide-band tracheids occur only in derived members, and
wide-band tracheids of North American Cactoideae are narrower and are aligned in a more orderly radial pattern than those
of South American Cactoideae. Wide-band tracheids probably arose at least three times in Cactaceae. 相似文献
33.
Reinhard Pinontoan Takashi Yuasa† ‡ Marinela I. Anderca Takashi Matsuoka Nobuyuki Uozumi Hitoshi Mori Shoshi Muto 《Journal of phycology》2000,36(3):545-552
A cDNA clone encoding a Ca2 +-dependent protein kinase (DtCPK1) with a calculated molecular mass of 65,746 Da was isolated by sequential immuno- and hybridization-screening from a cDNA library of the halotolerant green alga, Dunaliella tertiolecta Butcher (Chlorophyceae). Primary structure analysis of DtCPK1 revealed a long variable domain preceding a catalytic domain, an autoinhibitory junction domain, and a C-terminal calmodulin-like domain containing 4 EF-hand motifs. Database searches showed that DtCPK1 has a high similarity to CCK1 , a CDPK from the green alga, Chlamydomonas eugamentos Moewus . The N-terminal long variable domain of DtCPK1 contains neither the N-myristoylation motif, which is found in many CDPKs, nor the PEST motif, which is associated with rapid protein turnover and found in one CDPK subfamily. However, a putative Ca2 +-dependent lipid binding domain that might be responsible for the association of cytosolic DtCPK1 with the cell membrane was identified in the variable domain. Three CDPKs, with molecular masses of 62, 54, and 47 kDa respectively, were observed in an in-gel protein kinase assay of D. tertiolecta cells extract. No change in the activities of these CDPKs were observed for up to 30 min after D. tertiolecta cells had been subjected to a hypoosmotic shock. An antibody raised against a CDPK purified from D. tertiolecta and used to isolate the DtCPK1 cDNA clone cross-reacted strongly with the 62-kDa CDPK but weakly with the 54-kDa CDPK in a Western blot, indicating that the 62-kDa CDPK is identical to DtCPK1. There was no change in the intensity of these bands after hypoosmotic shock, implying that the cellular level of the enzyme protein is not associated with hypoosmotic shock. These results indicate that CDPK is activated only by the increase in cytosolic-free Ca2 + concentration in vivo . 相似文献
34.
Shin Deguchi Yumi Shimazaki Sunao Uozumi Keitaro Tawaraya Hidenori Kawamoto Osamu Tanaka 《Plant and Soil》2007,291(1-2):291-299
A field experiment was conducted to investigate the effects of white clover living mulch on the arbuscular mycorrhizal (AM)
fungus colonization of corn roots and the yield of silage corn. The following seven treatments were setup in a field that
had been kept bare by rotary tillage from August 2003 to July 2004: two white clover living mulch treatments without phosphorus
(P) application, with the white clover shoots clipped and removed or allowed to lie in place before sowing corn; one no-tillage
treatment without P application; and four rotary tillage treatments with different P application rates. White clover was broadcasted
in the living mulch treatments in August 2004. In June 2005, the white clover shoots in the living mulch treatments were clipped.
After tilling the four rotary tillage treatments, corn was sown in all the treatments. The fallow period before sowing corn
was 0 month (living mulch treatments) and 22 months (no-tillage and rotary tillage treatments). At knee high stage, the AM
fungus colonization of the corn roots and the P concentrations of the corn shoots in both the living mulch treatments were
increased relative to those in the other treatments. The yield of corn tended to increase in the no-tillage and rotary tillage
treatments with an increase in the P application rate. On the other hand, the yields of corn in the living mulch treatments
without the P application were not significantly different from the maximum yield among the no-tillage and rotary tillage
treatments. These results suggested that the white clover living mulch increased the yield of corn by facilitating the AM
fungus colonization and improving the P nutrition of corn. 相似文献
35.
Taurine inhibits apoptosis by preventing formation of the Apaf-1/caspase-9 apoptosome 总被引:5,自引:0,他引:5
Takatani T Takahashi K Uozumi Y Shikata E Yamamoto Y Ito T Matsuda T Schaffer SW Fujio Y Azuma J 《American journal of physiology. Cell physiology》2004,287(4):C949-C953
Cardiomyocyte apoptosis contributes to cell death during myocardial infarction. One of the factors that regulate the degree of apoptosis during ischemia is the amino acid taurine. To study the mechanism underlying the beneficial effect of taurine, we examined the interaction between taurine and mitochondria-mediated apoptosis using a simulated ischemia model with cultured rat neonatal cardiomyocytes sealed in closed flasks. Exposure to medium containing 20 mM taurine reduced the degree of apoptosis following periods of ischemia varying from 24 to 72 h. In the untreated group, simulated ischemia for 24 h led to mitochondrial depolarization accompanied by cytochrome c release. The apoptotic cascade was also activated, as evidenced by the activation of caspase-9 and -3. Taurine treatment had no effect on mitochondrial membrane potential and cytochrome c release; however, it inhibited ischemia-induced cleavage of caspase-9 and -3. Taurine loading also suppressed the formation of the Apaf-1/caspase-9 apoptosome and the interaction of caspase-9 with Apaf-1. These findings demonstrate that taurine effectively prevents myocardial ischemia-induced apoptosis by inhibiting the assembly of the Apaf-1/caspase-9 apoptosome. ischemia; cultured cardiomyocytes 相似文献
36.
Takashi Yamashita Naoto Tonouchi Takeshi Uozumi Teruhiko Beppu 《Molecular & general genetics : MGG》1987,210(3):462-467
Summary The aspartic protease gene of a zygomycete fungus Mucor pusillus was expressed in Saccharomyces cerevisiae under the control of the yeast GAL7 promoter. A putative preproenzyme with an NH2-terminal extension of 66 amino acids directed by the gene was processed in yeast cells and the mature enzyme, whose NH2-terminus was identical to that of the Mucor enzyme, was efficiently secreted into the medium at a concentration exceeding 150 mg/l. The enzyme secreted from the recombinant yeast was more glycosylated than the native Mucor enzyme but its enzymatic properties were almost identical with those of the native enzyme, which has been used as a milk coagulant in cheese manufacture. 相似文献
37.
Alejandro Vazquez-Tello Makoto Hidaka Takeshi Uozumi 《Plant Cell, Tissue and Organ Culture》1995,40(2):169-177
Embryogenic cell suspensions of Lavatera thuringiaca L. were established from leaf petiole and shoot regeneration was achieved when cells were plated on medium without growth regulators. We tested three methods for protoplast culture, isolated from a one-year old embryogenic cell suspension, to determine the best conditions for L. thuringiaca protoplast culture and shoot regeneration. The highest protoplast plating efficiency was obtained with the agaroseembedded method, reaching 30%, while the nursing culture method gave 5% when the protoplasts were plated over Whatman paper No. 2. However, the same nursing culture failed to produce protoplast-derived microcalluses when the protoplasts were plated on a nitrocellulose filter. The liquid thin layer method gave the lowest plating efficiency with only 0.5%. Shoot regeneration from protoplast-derived microcalluses was achieved in two steps; first, globular embryo development was favored in medium low in auxin (2,4-d and BA at 0.01 and 0.05 mg 1-1, respectively), second, the globular embryos further differentiate into shoots in medium without growth regulators or in medium containing GA3 (0.5 to 1.0 mg 1-1).Abbreviations 2,4-d
2,4-dichlorophenoxyacetic acid
- BA
benzyladenine
- GA3
gibberellic acid
- NAA
-naphthaleneacetic acid
- IBA
indole-3-butyric acid 相似文献
38.
Uozumi N Gao C Yoshioka T Nakano M Moriwaki K Nakagawa T Masuda T Tanabe M Miyoshi E 《Journal of proteome research》2010,9(12):6345-6353
Carbohydrate antigen 19-9 (CA19-9) is a well-known tumor marker for pancreatic cancer. Although the CA19-9 level is measured using anti-sialyl Lewis A antibodies, it remains unknown which molecules carry CA19-9 other than mucins. Here we report the identification and characterization of a novel type of CA19-9 carrier, BGM (bile globular membrane), which is thought to exist in normal bile and to be secreted into sera of patients with pancreatic cancer. We purified the BGM from bile juice using a β-casein column because surface plasmon resonance analysis could detect such carrier vesicles binding to β-casein in sera of patients with pancreatic cancer. We identified characteristic molecules for BGM such as AHNAK (desmoykoin) and a novel golgin family member, CABIN (CAsein Binding domain integral protein with golgIN motif) by mass spectrometry analysis. BGM was detected in the sera of patients with pancreatic cancer as well as athymic mice with transplanted pancreatic cancer cells. Down regulation of CABIN inhibited the secretion of CA19-9 on BGM in pancreatic cancer cell lines. We measured and visualized BGM in sera of patients with cancer. Thus, BGM might be another CA19-9 carrier (glyco-lipids on membrane vesicles) other than mucins and could be applied to the diagnosis of pancreatic cancer. 相似文献
39.
Uozumi N 《American journal of physiology. Cell physiology》2001,281(3):C733-C739
The value of theEscherichia coli expression system has long been establishedbecause of its effectiveness in characterizing the structure andfunction of exogenously expressed proteins. When eukaryotic membraneproteins are functionally expressed in E. coli, thisorganism can serve as an alternative to eukaryotic host cells. A fewexamples have been reported of functional expression of animal andplant membrane proteins in E. coli. This mini-review describes the following findings: 1) homologousK+ transporters exist in prokaryotic cells and ineukaryotic cells; 2) plant K+ transporters canfunctionally complement mutant K+ transporter genes inE. coli; and 3) membrane structures of plant K+ transporters can be elucidated in an E. colisystem. These experimental findings suggest the possibility ofutilizing the E. coli bacterium as an expression system forother eukaryotic membrane transport proteins. 相似文献
40.
Umemura K Satou J Iwata M Uozumi N Koga J Kawano T Koshiba T Anzai H Mitomi M 《The Plant journal : for cell and molecular biology》2009,57(3):463-472
Systemic acquired resistance (SAR), a natural disease response in plants, can be induced chemically. Salicylic acid (SA) acts as a key endogenous signaling molecule that mediates SAR in dicotyledonous plants. However, the role of SA in monocotyledonous plants has yet to be elucidated. In this study, the mode of action of the agrochemical protectant chemical probenazole was assessed by microarray-based determination of gene expression. Cloning and characterization of the most highly activated probenazole-responsive gene revealed that it encodes UDP-glucose:SA glucosyltransferase (OsSGT1) , which catalyzes the conversion of free SA into SA O- β-glucoside (SAG). We found that SAG accumulated in rice leaf tissue following treatment with probenazole or 2,6-dichloroisonicotinic acid. A putative OsSGT1 gene from the rice cultivar Akitakomachi was cloned and the gene product expressed in Escherichia coli was characterized, and the results suggested that probenazole-responsive OsSGT1 is involved in the production of SAG. Furthermore, RNAi-mediated silencing of the OsSGT1 gene significantly reduced the probenazole-dependent development of resistance against blast disease, further supporting the suggestion that OsSGT1 is a key mediator of development of chemically induced disease resistance. The OsSGT1 gene may contribute to the SA signaling mechanism by inducing up-regulation of SAG in rice plants. 相似文献