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Hirota, Noriaki; Takeda, Kiyoko*; Tachibana, Yukio; Masaki, Yasuhiro*
Zairyo To Kankyo, 70(3), p.68 - 76, 2021/03
Corrosion resistance of stainless steels and Ni-based alloys were evaluated in a sulfuric acid decomposition gas at high temperature. The evaluation were carried out in an environment simulated in the sulfuric acid decomposition reaction vessel for thermochemical hydrogen production process (IS process). Their corrosion films were also analyzed for better understanding of the corrosion behavior. As a result, after 100 hour corrosion test, Ni-based alloy containing 2.4% Si showed good corrosion resistance. Ferritic stainless steel containing 3% Al (3Al-Ferrite) showed better corrosion resistance. Its corrosion rate was lower than that of SiC (0.1mm/year), which is a candidate material for the sulfuric acid decomposition reaction vessel. On the other hand, Ni-based alloy pre-filmed with Al
O
is prepared as the relative corrosion film of 3Al-Ferrite. Its corrosion rate was significantly higher than that of 3Al-Ferrite. As the result of EPMA analysis of these oxide films, Ni-based alloy containing 2.4% Si formed Si oxide film which had some cracks after the long term corrosion test. Therefore S penetrated into grain boundaries of the matrix through the oxide film. 3Al-Ferrite formed a thin and uniform Al
O
film, and the penetration of S into the grain boundaries was not observed. Al
O
pre-film of Ni-based alloy also showed S penetration in the matrix because the Al
O
pre-film had many small defects originally. The corrosion oxide film of 3Al-Ferrite consisted of only
-Al
O
, while the Al
O
pre-film consist of
-Al
O
and
-Al
O
. Those results suggest that the better corrosion resistance of 3Al-Ferrite is due to the uniform formation of dense
-Al
O
film at the early stage of the corrosion.
with
under high salt conditions using the ion beam mutation breedingMaruyama, Yudai*; Takeda, Kiyoko*; Tomooka, Norihiko*; Sato, Katsuya; Ono, Yutaka; Yokoyama, Tadashi*
JAEA-Review 2015-022, JAEA Takasaki Annual Report 2014, P. 99, 2016/02
sp. ME121, isolated from soil as a mixed single colony with
sp. 32KFujinami, Shun*; Takeda, Kiyoko*; Onodera, Takefumi*; Sato, Katsuya; Shimizu, Tetsu*; Wakabayashi, Yu*; Narumi, Issey*; Nakamura, Akira*; Ito, Masahiro*
Genome Announcements (Internet), 3(5), p.e01005-15_1 - e01005-15_2, 2015/09
USDA110 generated by ion-beam irradiationTakeda, Kiyoko*; Sato, Katsuya; Narumi, Issey*; Ono, Yutaka; Otsu, Naoko*; Yokoyama, Tadashi*
JAEA-Review 2014-050, JAEA Takasaki Annual Report 2013, P. 120, 2015/03
sp. strain TCA20, isolated from a hot spring containing a high concentration of calcium ionsFujinami, Shun*; Takeda, Kiyoko*; Onodera, Takefumi*; Sato, Katsuya; Sano, Motohiko*; Takahashi, Yuka*; Narumi, Issey*; Ito, Masahiro*
Genome Announcements (Internet), 2(5), p.e00866-14_1 - e00866-14_2, 2014/09
sp. strain TS-2, isolated from a jumping spiderFujinami, Shun*; Takeda, Kiyoko*; Onodera, Takefumi*; Sato, Katsuya; Sano, Motohiko*; Narumi, Issey*; Ito, Masahiro*
Genome Announcements (Internet), 2(3), p.e00458-14_1 - e00458-14_2, 2014/05
USDA110 generated by ion-beam irradiationTakeda, Kiyoko; Sato, Katsuya; Narumi, Issey*; Otsu, Naoko*; Yokoyama, Tadashi*
JAEA-Review 2013-059, JAEA Takasaki Annual Report 2012, P. 114, 2014/03

Sato, Katsuya; Onodera, Takefumi*; Takeda, Kiyoko; Narumi, Issey*
JAEA-Review 2013-059, JAEA Takasaki Annual Report 2012, P. 110, 2014/03
sp. strain TS-1Fujinami, Shun*; Takeda, Kiyoko; Onodera, Takefumi*; Sato, Katsuya; Sano, Motohiko*; Narumi, Issey*; Ito, Masahiro*
Genome Announcements (Internet), 1(6), P. e01043-13, 2013/12
USDA110 generated by ion-beam irradiationTakeda, Kiyoko; Tejima, Kohei*; Sato, Katsuya; Narumi, Issei; Yokoyama, Tadashi*
JAEA-Review 2012-046, JAEA Takasaki Annual Report 2011, P. 107, 2013/01
-sterilization of biofertilizer's carrier on bacterial inoculants survivalTejima, Kohei*; Yokoyama, Tadashi*; Sato, Katsuya; Takeda, Kiyoko; Narumi, Issei
JAEA-Review 2012-046, JAEA Takasaki Annual Report 2011, P. 112, 2013/01
-sterilization of carrier materials made with different types of soils on the shelf life of biofertilizer containing
strain USDA110Tejima, Kohei; Sato, Katsuya; Takeda, Kiyoko; Yokoyama, Tadashi*; Narumi, Issei
Radioisotopes, 61(4), p.161 - 171, 2012/04
A biofertilizer is a substance that holds beneficial microorganisms for plant growth in a carrier material. To demonstrate the effect of
-sterilization, the survival of the
was monitored to assess the shelf life of biofertilizers. As biofertilizer carriers, five kinds of typical Japanese soil-based materials were used. Following the sterilization of carrier materials by
-irradiation or autoclaving,
was inoculated into each material. The biofertilizer was stored for 12 months at 4
C or 30
C. After storage, viable inoculants in the biofertilizer were enumerated. Results indicated that inoculant density after storage was greater than the initial density in biofertilizers made from sterilized carriers, whereas it decreased significantly in biofertilizers made from non-sterilized carriers.
-sterilization was superior to autoclave sterilization in enhancing inoculant survival in some cases.
USDA 110 obtained by ion-beam microbial mutation-breeding technologyTakeda, Kiyoko; Tejima, Kohei; Sato, Katsuya; Narumi, Issei; Yokoyama, Tadashi*
JAEA-Review 2011-043, JAEA Takasaki Annual Report 2010, P. 110, 2012/01
USDA 110 into a high temperature tolerant strain in terms of ion-beam microbial mutation-breeding technologyTakeda, Kiyoko*; Tejima, Kohei; Sato, Katsuya; Narumi, Issei; Yokoyama, Tadashi*
JAEA-Review 2010-065, JAEA Takasaki Annual Report 2009, P. 75, 2011/01
by ion beam irradiationTakeda, Kiyoko; Tejima, Kohei; Sato, Katsuya; Narumi, Issei; Yokoyama, Tadashi*
no journal, ,
In Asian countries, many researchers are trying to develop biofertilizers. Major constraint of biofertilizer utilization is a viability loss of beneficial microorganisms caused by high temperature stress during both storage and transportation. Therefore, we have tried to improve high temperature tolerance of soybean nodule bacterium. Consequently, we have obtained 20 high temperature tolerant mutants, which can survive at 43
C for 7 days. We also successfully generated 5 mutants, which can survive at 47
C for 3 days by re-irradiation to mutants that survive at 43
C for 7 days. On the other hand, we found some phenotypic changes of high temperature tolerant mutants. For example, the colony of these mutants was glossy pale pink color unlike wild type. And the generation time of these mutants at 30
C was about 1.5 h shorter than that of wild type. There might be a link between high temperature tolerance and these phenotypic changes.
USDA110 generated by ion-beam irradiationTakeda, Kiyoko; Sato, Katsuya; Narumi, Issey*; Otsu, Naoko*; Yokoyama, Tadashi*
no journal, ,
With the aims of utilization as a biofertilizer inoculant and elucidation of high-temperature tolerance mechanism of soybean nodule bacteria, we had applied the ion beam breeding technology to a strain
(
) USDA110. Consequently, we obtained a mutant named M14 which was able to maintain high viable cell numbers under high-temperature (42
C) for at least 7 days. Genome comparison with USDA110 revealed that (1) 1.27 Mbp inversion mutagenesis and (2) 18 single base mutations were occurred in M14. This study was the first attempt to apply the ion beam breeding technology to a prokaryote and succeeded in proving the effectiveness of it.
Takeda, Kiyoko*; Tejima, Kohei; Sato, Katsuya; Narumi, Issei; Yokoyama, Tadashi*
no journal, ,
no abstracts in English
USDA110 into a high temperature tolerant strain in terms of ion-beam microbial mutation-breeding technologyTakeda, Kiyoko*; Tejima, Kohei; Sato, Katsuya; Narumi, Issei; Yokoyama, Tadashi*
no journal, ,
no abstracts in English
USDA110 generated by ion-beam irradiationTakeda, Kiyoko; Sato, Katsuya; Narumi, Issey*; Otsu, Naoko*; Yokoyama, Tadashi*
no journal, ,

Sato, Katsuya; Onodera, Takefumi*; Takeda, Kiyoko; Narumi, Issey*
no journal, ,
In this study, we investigated mutant frequencies of two different antibiotic-resistant mutants for carbon ion beams in
and identified the mutation sites in the streptomycin-resistant (Sm
) mutants. The Sm
mutant frequencies increased depending on radiation dose. It seems that this dose range is the best dose to generate the mutants of interest for research and breeding purpose. Four kinds of mutation sites at the
locus were determined from 8 Sm
mutants. These mutations cause amino acid substitutions at position 43 (Lys to Thr or Arg) and 88 (Lys to Glu or Arg) in the S12 protein, respectively. The two hot spots at Lys43 and Lys88 in the S12 protein might be a binding target of streptomycin or adjacent to the center of streptomycin interaction with the ribosome.