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Dive into the research topics where Kazuyuki Hirayae is active.

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Featured researches published by Kazuyuki Hirayae.


Journal of General Plant Pathology | 2001

Synergistic Antifungal Activity of Chitinolytic Enzymes and Prodigiosin Produced by Biocontrol Bacterium, Serratia marcescens Strain B2 against Gray Mold Pathogen, Botrytis cinerea

Nobutaka Someya; Masami Nakajima; Kazuyuki Hirayae; Tadaaki Hibi; Katsumi Akutsu

Serratia marcescensstrain B2 is an effective biocontrol agent against gray mold of cyclamen, caused by Botrytis cinerea Persoon. Strain B2 has strong antifungal activity against B. cinerea in vitro. The culture filtrate was found to contain different types of chitinolytic enzyme activity, including endochitinase and chitobiase activity. Four chitinolytic enzymes were detected among the extracellular proteins of strain B2. Two major enzymes, a 58-kDa endochitinase and a 98-kDa chitobiase, were purified by chromatography and electrofocusing, respectively. Both enzymes inhibited spore germination of B. cinerea. And a red pigment, prodigiosin, extracted and purified from the bacterial cells, also inhibited spore germination. When prodigiosin and the chitinolytic enzymes were applied in concert, a synergistic inhibitory effect was observed. S. marcescens strain B2 has multiple modes of action against the pathogen.


Phytochemistry | 1997

Pectinolytic enzymes from Pseudomonas marginalis MAFF 03-01173.

Kaeko Hayashi; Yasushi Inoue; Manabu Shiga; Shin-ichi Sato; Ryo Takano; Kazuyuki Hirayae; Tadaaki Hibi; Saburo Hara

Two pectinolytic enzymes were purified from the culture broth of Pseudomonas marginalis pv. marginalis MAFF 03-01173 with total 33% recovery of the initial activity. From the substrate specificities against pectin and polygalacturonic acid, the requirement of calcium ion for the enzymatic activity, and the N-terminal sequences, the enzymes were identified as pectin lyase and pectate lyase. The M,s of pectin lyase and pectate lyase were estimated to be 34,000 and 43,000, respectively, by SDS polyacrylamide gel electrophoresis. Both enzymes showed almost the same pH dependent activity curves with the highest activity at pH 8.3


Journal of General Plant Pathology | 2011

A refined inoculation method to evaluate false smut resistance in rice

Taketo Ashizawa; Mami Takahashi; Jouji Moriwaki; Kazuyuki Hirayae

False smut, caused by Ustilaginoideavirens, is a serious disease of rice worldwide. To evaluate false smut resistance in rice, we developed a method combining the cultivation of the main culm of rice plants in the greenhouse and rapid preparation of a conidial suspension to inject into the leaf sheath. The method was used to evaluate false smut resistance in 18 varieties/lines of rice. For comparison, field trials were also carried out in 2007 and 2008. The results indicated that the greenhouse method was more reproducible than field trials: commercial varieties tested were resistant; almost all the forage varieties were highly susceptible; and blast-resistant varieties/lines were mostly resistant to false smut. Thus, this inoculation method will be useful for determining the level of false smut resistance in rice and for breeding resistant varieties.


Journal of General Plant Pathology | 2015

Rapid PCR technique to detect QoI-resistant strains of Magnaporthe oryzae

Keiko Hayashi; Taketo Ashizawa; Takahide Sasaya; Kazuyuki Hirayae; Yuriko Hayano-Saito; Fumihiko Suzuki

The emergence of Magnaporthe oryzae strains with resistance to quinone outside inhibitor (QoI) fungicides necessitates the development of easy techniques for the rapid, sensitive monitoring of such strains. A QoI-resistant mutant and a wild-type strain showed a single nucleotide polymorphism (SNP). For simple, fast, low-cost, and reliable detection of this SNP, we developed two types of PCR-based DNA markers that enable easy detection of resistant strains by using DNA templates prepared from filter paper permeated with the fungus. The method enabled us to obtain reliable results by using a detection procedure that takes only a few hours without special kits.


Journal of General Plant Pathology | 2015

Gibberella ear rot of corn caused by Fusarium asiaticum in Japan

Akira Kawakami; Naoki Kato; Takahide Sasaya; Keisuke Tomioka; Hiroyoshi Inoue; Atsushi Miyasaka; Kazuyuki Hirayae

Ear rot with white or pink mold was found on corn (Zea mays L.). A species of Fusarium, not registered previously as a pathogen causing Gibberella ear rot of corn in Japan, was isolated from the rotted ear. The isolates, identified as F. asiaticum based on morphological characteristics and nucleotide sequences, caused white or pink mold on corn ear after inoculation. Moreover, the 3-acetyl deoxynivalenol chemotype and the nivalenol chemotype were found in the isolates. We propose to include F. asiaticum as one of the pathogens causing Gibberella ear rot of corn in Japan.


Japanese Journal of Phytopathology | 1993

Growth Inhibition of Botrytis spp. by Serratia marcescens B2 Isolated from Tomato Phylloplane

Katsumi Akutsu; Akiko Hirata; Michiko Yamamoto; Kazuyuki Hirayae; Satoshi Okuyama; Tadaaki Hibi


Japanese Journal of Phytopathology | 1996

Biological Control of Cyclamen Gray Mould (Botrytis cinerea) by Serratia marcescens B2

Hiroyuki Iyozumi; Tomoyuki Komagata; Kazuyuki Hirayae; Kenichi Tsuchiya; Tadaaki Hibi; Katsumi Akutsu


Applied Entomology and Zoology | 2003

Discrimination of Japanese isolates of Beauveria brongniartii (Deuteromycotina: Hyphomycetes) by RFLP of the rDNA-ITS regions

Sanae Wada; Mitsuo Horita; Kazuyuki Hirayae; Mitsuaki Shimazu


Japanese Journal of Phytopathology | 1996

In Vitro Growth Inhibition of Plant Pathogenic Fungi, Botrytis spp., by Escherichia coli Transformed with a Chitinolytic Enzyme Gene from a Marine Bacterium, Alteromonas sp. Strain 79401

Kazuyuki Hirayae; Akiko Hirata; Katsumi Akutsu; Saburo Hara; Ilkka Havukkala; Yoko Nishizawa; Tadaaki Hibi


Japanese Journal of Phytopathology | 1996

Comparative RFLP Profiles among Representative Strains of Japanese Races of Xanthomonas oryzae pv. oryzae Using the Repetitive DNA Probe pJEL101

Hisatoshi Kaku; Kazuyuki Hirayae; Hirokazu Ochiai; Satoko Kanematsu; Takahito Noda; Kenichi Tsuchiya; Tadaaki Hibi

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Kenichi Tsuchiya

Tokyo University of Agriculture

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Taketo Ashizawa

National Agriculture and Food Research Organization

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Saburo Hara

Kyoto Institute of Technology

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Takahide Sasaya

National Agriculture and Food Research Organization

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