Hidemi Kitano

Hidemi Kitano

Auto-generated profile, based on publicly available information

Hidemi Kitano

Bioscience and Biotechnology Center, Nagoya University, Furo, Chikusa, Nagoya, Aichi, 464-8601, Japan.

Research Focus & Metrics

Academic Career Length

27Years (2000-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
19 December 2006 in Plant Molecular Biology
Verified
Journal Article
Open access
PDF file
AMAkio Miyao
Akio Miyao
YIYukimoto Iwasaki
Yukimoto Iwasaki
HKHidemi Kitano
Hidemi Kitano
JIJun-Ichi Itoh
Jun-Ichi Itoh
MMMasahiko Maekawa
Masahiko Maekawa
HHHirohiko Hirochika
Hirohiko Hirochika
In order to facilitate the functional analysis of rice genes, we produced about 50,000 insertion lines with the endogenous retrotransposon Tos17. Phenotypes of these lines in the M2 generation were observed in the field and characterized based on 53 phenotype descriptors. Nearly half of the lines showed more than one mutant phenotype. The most frequently observed phenotype was low fertility, followed by dwarfism. Phenotype data with photographs of each line are stored in the Tos17 mutant panel web-based database with a dataset of sequences flanking Tos17 insertion points in the rice genome (http://tos.nias.affrc.go.jp/). This combination of phenotypic and flanking sequence data will stimulate the functional analysis of rice genes.

27 February 2012 in Rice
Verified
Journal Article
Open access
PDF file
SSShuhei Segami
Shuhei Segami
IKIzumi Kono
Izumi Kono
TATsuyu Ando
Tsuyu Ando
MYMasahiro Yano
Masahiro Yano
HKHidemi Kitano
Hidemi Kitano
YIYukimoto Iwasaki
Yukimoto Iwasaki
Seed size is an important trait in determinant of rice seed quality and yield. In this study, we report a novel semi-dominant mutant S mall and r ound s eed 5 (Srs5) that encodes alpha-tubulin protein. Lemma cell length was reduced in Srs5 compared with that of the wild-type. Mutants defective in the G-protein alpha subunit (d1-1) and brassinosteroid receptor, BRI1 (d61-2) also exhibited short seed phenotypes, the former due to impaired cell numbers and the latter due to impaired cell length. Seeds of the double mutant of Srs5 and d61-2 were smaller than those of Srs5 or d61-2. Furthermore, SRS5 and BRI1 genes were highly expressed in Srs5 and d61-2 mutants. These data indicate that SRS5 independently regulates cell elongation of the brassinosteroid signal transduction pathway

2 February 2016 in Biotechnology for Biofuels
Verified
Journal Article
Open access
PDF file
HTHiroshi Teramura
Hiroshi Teramura
KSKengo Sasaki
Kengo Sasaki
TOTomoko Oshima
Tomoko Oshima
FMFumio Matsuda
Fumio Matsuda
MOMami Okamoto
Mami Okamoto
AKAkihiko Kondo
Akihiko Kondo
The primary components of lignocellulosic biomass such as sorghum bagasse are cellulose, hemicellulose, and lignin. Each component can be utilized as a sustainable resource for producing biofuels and bio-based products. However, due to their complicated structures, fractionation of lignocellulosic biomass components is required. Organosolv pretreatment is an attractive method for this purpose. However, as organosolv pretreatment uses high concentrations of organic solvents (>50 %), decreasing the concentration necessary for fractionation would help reduce processing costs. In this study, we sought to identify organic solvents capable of efficiently fractionating sorghum bagasse components at low concentrations. Five alcohols (ethanol, 1-propanol, 2-propanol, 1-butanol, and 1-pentanol) were used for organosolv pretreatment of sorghum bagasse at a concentration of 12.5 %. Sulfuric acid (1 %) was used as a catalyst. With 1-butanol and 1-pentanol, three fractions (black liquor, liquid fraction containing xylose, and cellulose-enriched solid fraction) were obtained after pretreatment. Two-dimensional nuclear magnetic resonance analysis revealed that the lignin aromatic components of raw sorghum bagasse were concentrated in the black liquor fraction, although the major lignin side-chain (β-O-4 linkage) was lost. Pretreatment with 1-butanol or 1-pentanol effectively removed p-coumarate, some guaiacyl, and syringyl. Compared with using no solvent, pretreatment with 1-butanol or 1-pentanol resulted in two-fold greater ethanol production from the solid fraction by Saccharomyces cerevisiae. Our results revealed that a low concentration (12.5 %) of a highly hydrophobic solvent such as 1-butanol or 1-pentanol can be used to separate the black liquor from the solid and liquid fractions. The efficient delignification and visible separation of the lignin-rich fraction possible with this method simplify the fractionation of sorghum bagasse.

1 September 2000 in The Plant Cell
Verified
Journal Article
Open access
CYChizuko Yamamuro
Chizuko Yamamuro
YIYoshihisa Ihara
Yoshihisa Ihara
XWXiong Wu
Xiong Wu
TNTakahiro Noguchi
Takahiro Noguchi
SFShozo Fujioka
Shozo Fujioka
MMMakoto Matsuoka
Makoto Matsuoka

21 August 2018 in Scientific Reports
Verified
Journal Article
Open access
PDF file
YFYasuko Fujishiro
Yasuko Fujishiro
AAAyumi Agata
Ayumi Agata
SOSadayuki Ota
Sadayuki Ota
RIRyota Ishihara
Ryota Ishihara
YTYasumi Takeda
Yasumi Takeda
HKHidemi Kitano
Hidemi Kitano
Rice grain number directly affects crop yield. Identifying alleles that improve panicle architecture would greatly aid the development of high-yield varieties. Here, we show that the quantitative trait locus qSrn7 contains rice FRIZZY PANICLE (FZP), a previously reported gene encoding an ERF transcription factor that promotes floral transition. Reduced expression of FZP in the reproductive stage increases the extent of higher order branching of the panicle, resulting in increased grain number. Genotype analysis of this gene in cultivars from the publicly available National Institute of Agrobiological Sciences (NIAS) Core Collection demonstrated that the extent of higher order branching, especially in the upper panicle, was increased in those cultivars carrying the FZP allele associated with qSrn7. Furthermore, chromosome segment substitution lines resulting from a cross between Koshihikari and Kasalath, the latter of which carries qSrn7/FZP, also showed that upper panicle higher order branching and grain yield were increased by qSrn7/FZP. Our findings indicate that qSrn7/FZP influences panicle branching pattern and is thus useful in the breeding of high-yield rice varieties.

25 July 2016 in Rice
Verified
Journal Article
Open access
PDF file
SSShuhei Segami
Shuhei Segami
TYTatsuya Yamamoto
Tatsuya Yamamoto
KOKatsuyuki Oki
Katsuyuki Oki
TNTomonori Noda
Tomonori Noda
HKHiroyuki Kanamori
Hiroyuki Kanamori
KMKotaro Miura
Kotaro Miura
Grain size is an important trait that affects rice yield. Although many genes that contribute to grain size have been cloned from mutants or by quantitative trait locus (QTL) analysis based on bi-parental mapping, the molecular mechanisms underlying grain-size determination remain poorly understood. In this study, we identified the lines with the largest grain size and detected novel QTLs affecting the grain size. We screened the National Institute for Agrobiological Sciences Genebank database and identified two rice lines, BG23 with the widest grain and LG10 with the longest grain. Using these two lines, we performed QTL analysis for grain size. Eight QTLs were detected during the QTL analyses using F2 populations derived from crosses between the large-grain lines BG23 or LG10 and the middle-size grain cultivars Nipponbare and Kasalath. Both BG23 and LG10 possessed large-grain alleles of four major QTLs: GW2, GS3, qSW5/GW5, and GW8. Other three minor QTLs were derived from BG23. However, these QTLs did not explain the differences in grain size between these two lines. Additionally, four QTLs for grain length or width were detected in an F2 population derived from a cross between BG23 and LG10; this population lacked the strong effects of the four major QTLs shared by both parent plants. Of these newly detected QTLs, the effects of two QTLs, GL3b and GL6, were confirmed by progeny testing. Comparison of the length of inner epidermal cells in plants homozygous for BG23 and LG10 alleles indicated that GL3b and GL6 genes regulate cell elongation and cell division, respectively. In this study, we detected 12 loci including 14 QTLs regulating grain size from two lines with largest grains available in Japanese stock. Of these loci, we confirmed the effect of two gene loci and mapped their candidate region. Identification of novel genes regulating grain size will contribute to our understanding of the molecular mechanisms controlling grain size.