Mamoru Yamada

Prof. Dr. Mamoru Yamada

Department of Biological Chemistry, Faculty of Agriculture, Life Science, Graduate School of Science and Technology for Innovation and Research Center for Thermotolerant Microbial Resources, Yamaguchi University, Yamaguchi, Japan
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Research Focus & Metrics

Academic Career Length

37Years (1990-Present)

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

Representative Publications

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18 March 2015 in Biotechnology for Biofuels
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Journal Article
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NLNoppon Lertwattanasakul
Noppon Lertwattanasakul
TKTommoyuki Kosaka
Tommoyuki Kosaka
AHAkira Hosoyama
Akira Hosoyama
YSYutaka Suzuki
Yutaka Suzuki
NRNadchanok Rodrussamee
Nadchanok Rodrussamee
Mamoru YamadaMamoru Yamada
Mamoru Yamada
High-temperature fermentation technology with thermotolerant microbes has been expected to reduce the cost of bioconversion of cellulosic biomass to fuels or chemicals. Thermotolerant Kluyveromyces marxianus possesses intrinsic abilities to ferment and assimilate a wide variety of substrates including xylose and to efficiently produce proteins. These capabilities have been found to exceed those of the traditional ethanol producer Saccharomyces cerevisiae or lignocellulose-bioconvertible ethanologenic Scheffersomyces stipitis. The complete genome sequence of K. marxianus DMKU 3-1042 as one of the most thermotolerant strains in the same species has been determined. A comparison of its genomic information with those of other yeasts and transcriptome analysis revealed that the yeast bears beneficial properties of temperature resistance, wide-range bioconversion ability, and production of recombinant proteins. The transcriptome analysis clarified distinctive metabolic pathways under three different growth conditions, static culture, high temperature, and xylose medium, in comparison to the control condition of glucose medium under a shaking condition at 30°C. Interestingly, the yeast appears to overcome the issue of reactive oxygen species, which tend to accumulate under all three conditions. This study reveals many gene resources for the ability to assimilate various sugars in addition to species-specific genes in K. marxianus, and the molecular basis of its attractive traits for industrial applications including high-temperature fermentation. Especially, the thermotolerance trait may be achieved by an integrated mechanism consisting of various strategies. Gene resources and transcriptome data of the yeast are particularly useful for fundamental and applied researches for innovative applications.

8 April 2011 in Applied Microbiology and Biotechnology
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Journal Article
Closed access
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NRNadchanok Rodrussamee
Nadchanok Rodrussamee
NLNoppon Lertwattanasakul
Noppon Lertwattanasakul
KHKatsushi Hirata
Katsushi Hirata
SUSuprayogi
Suprayogi
SLSavitree Limtong
Savitree Limtong
Mamoru YamadaMamoru Yamada
Mamoru Yamada

6 January 2023 in Fermentation
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Journal Article
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HKHaruthairat Kitwetcharoen
Haruthairat Kitwetcharoen
LPLy Tu Phung
Ly Tu Phung
PKPreekamol Klanrit
Preekamol Klanrit
STSudarat - Thanonkeo
Sudarat - Thanonkeo
PTPatcharaporn Tippayawat
Patcharaporn Tippayawat
PTPornthap Thanonkeo
Pornthap Thanonkeo
Kombucha, one of the ordinary fermented beverages consumed worldwide, is produced by fermenting tea and sugar with a symbiotic culture of bacteria and yeasts or so-called SCOBY. Kombucha can be made from different types of tea, such as black, green, white, red, and oolong teas, yielding various health benefits and properties. Several species of bacteria and yeasts are involved in the fermentation process, which generates many beneficial compounds, such as polyphenols, organic acids, amino acids, vitamins, minerals, organic nitrogens, and hydrolytic enzymes, which have significant health effects and therapeutic properties, such as antioxidant, anti-inflammatory, anticancer, and antimicrobial properties. This review describes recent research on kombucha fermentation, the microbial community in SCOBY, the chemical composition of kombucha, and its health benefits. The adverse effects and prospects of kombucha production were also discussed.

10 June 2011 in PLOS ONE
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Journal Article
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MMMasayuki Murata
Masayuki Murata
HFHiroko Fujimoto
Hiroko Fujimoto
KNKaori Nishimura
Kaori Nishimura
KCKannikar Charoensuk
Kannikar Charoensuk
HNHiroshi Nagamitsu
Hiroshi Nagamitsu
Mamoru YamadaMamoru Yamada
Mamoru Yamada
The molecular mechanism supporting survival at a critical high temperature (CHT) in Escherichia coli was investigated. Genome-wide screening with a single-gene knockout library provided a list of genes indispensable for growth at 47°C, called thermotolerant genes. Genes for which expression was affected by exposure to CHT were identified by DNA chip analysis. Unexpectedly, the former contents did not overlap with the latter except for dnaJ and dnaK, indicating that a specific set of non-heat shock genes is required for the organism to survive under such a severe condition. More than half of the mutants of the thermotolerant genes were found to be sensitive to H2O2 at 30°C, suggesting that the mechanism of thermotolerance partially overlaps with that of oxidative stress resistance. Their encoded enzymes or proteins are related to outer membrane organization, DNA double-strand break repair, tRNA modification, protein quality control, translation control or cell division. DNA chip analyses of essential genes suggest that many of the genes encoding ribosomal proteins are down-regulated at CHT. Bioinformatics analysis and comparison with the genomic information of other microbes suggest that E. coli possesses several systems for survival at CHT. This analysis allows us to speculate that a lipopolysaccharide biosynthesis system for outer membrane organization and a sulfur-relay system for tRNA modification have been acquired by horizontal gene transfer.

1 August 2005 in Microbiology
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Journal Article
Open access
SKShahinur Kabir
Shahinur Kabir
DYDaisuke Yamashita
Daisuke Yamashita
SKSatoshi Koyama
Satoshi Koyama
TOTaku Oshima
Taku Oshima
KKKen Kurokawa
Ken Kurokawa
Mamoru YamadaMamoru Yamada
Mamoru Yamada
It has been shown thatEscherichia colicells with increased expression of therpoEgene encodingσEexhibit enhanced cell lysis in early stationary phase. Further analysis of the lysis phenomenon was performed using a transient expression system of therpoEgene and by DNA microarray. The former analysis revealed aσE-directed cell lysis, specific for early stationary phase but not for the exponential phase. The microarray analysis with RNAs from exponential and early stationary phase cells revealed that a large number of genes were up- or down-regulated when therpoEgene was induced, and that several genes were induced in a phase-specific manner. The upregulated genes include many previously identifiedσEregulon genes, suggesting that a large number of genes are under the control ofσEin this organism. These genes are involved in various cellular activities, including the cell envelope, cellular processes, regulatory functions, transport and translation. Genes that are presumably related to phase-specific cell lysis inE. coliare discussed.

19 July 2011 in AMB Express
Verified
Journal Article
Open access
NLNoppon Lertwattanasakul
Noppon Lertwattanasakul
NRNadchanok Rodrussamee
Nadchanok Rodrussamee
SUSuprayogi
Suprayogi
SLSavitree Limtong
Savitree Limtong
PTPornthap Thanonkeo
Pornthap Thanonkeo
Mamoru YamadaMamoru Yamada
Mamoru Yamada
Kluyveromyces marxianus possesses a useful potential to assimilate a wide variety of substrates at a high temperature, but the negative effect by coexisting glucose is critical for utilization of biomass containing various sugars. Such a negative effect on the activity of inulinase, which is the sole enzyme to hydrolyze sucrose, raffinose and inulin, has been demonstrated in K. marxianus without analysis at the gene level. To clarify the utilization capability of sucrose, raffinose and inulin and the glucose effect on inulinase in K. marxianus DMKU 3-1042, its growth and metabolite profiles on these sugars were examined with or without glucose under a static condition, in which glucose repression evidently occurs. Consumption of sucrose was not influenced by glucose or 2-deoxyglucose. On the other hand, raffinose and inulin consumption was hampered by glucose at 30°C but hardly hampered at 45°C. Unlike Saccharomyces cerevisiae, increase in glucose concentration had no effect on sucrose utilization. These sugar-specific glucose effects were consistent with the level of inulinase activity but not with that of the KmINU1 transcript, which was repressed in the presence of glucose via KmMig1p. This inconsistency may be due to sufficient activity of inulinase even when glucose is present. Our results encourage us to apply K. marxianus DMKU 3-1042 to high-temperature ethanol fermentation with biomass containing these sugars with glucose.