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PRIHARDI KaharEngineering Biology Research CenterAssociate Professor
Researcher basic information
■ Research Keyword- Oleogenous microbial engineering
- Biodegradable polymer
- Synthetic biology
- Metabolic engineering
- Genome Biology
- Bioproduction platform development
- Bioresource technology
- Nanotechnology/Materials / Polymer chemistry / Biopolymer Chemistry and Science
- Environmental science/Agricultural science / Environmental materials/recycling technology / Biomaterial and Recycle Science
- Manufacturing technology (mechanical, electrical/electronic, chemical engineering) / Applied biofunctional and bioprocess engineering / Biotechnology and Bioprocess Engineering
- Environmental science/Agricultural science / Biological resource conservation / Conservation Biology and Bioresources
- Life sciences / Genomics / Genome Biology
- Life sciences / Applied biochemistry / Applied Biochemistry
Research activity information
■ Award- Apr. 2023 藤森科学研究財団, 研究助成
- Mar. 2023 The Society of Chemical Engineers, Japan, 25th SCEJ Excellent award, Malic acid assimilation by yeast cells with surface display of esterase
- Nov. 2021 Young Asian Biological Engineer’s community (YABEC), Metabolic engineering of Saccharomyces cerevisiae BTCC3 for rapid gypsum-free lactic acid fermentation
- Oct. 2016 Kobe University, Faculty of Engineering, Department of Chemical Science and Engineering, Certificate of Appreciation from the Dean of the Department of Chemical Science and Engineering
- 2004 International Symposium on Biological Polyesters (ISBP), The Prominent Poster Award, Effective Production and Kinetic Characteristic of Ultra-high-molecular-weight of PHB in Recombinant Escherichia coliInternational society
- Apr. 1998 公益財団法人橋谷奨学金
- Apr. 1997 Sato Yo International Scholarship Foundation, Satoh Foundation Fellowship
- Apr. 1992 Ministry of Research and Technology of Indonesia, Fellow of STAID (Science Technology for Industrial Development), Ministry of Research and Technology of Indonesia
- Mar. 2025, Microorganisms[Refereed][Invited]Scientific journal
- Jan. 2025, Molecules[Refereed]Scientific journal
- Corresponding, Jan. 2025, Processes[Refereed][Invited]Scientific journal
- Corresponding, Jan. 2025, Fermentation[Refereed]Scientific journal
- Oct. 2024, Biomass Conversion and Biorefinery[Refereed]Scientific journal
- BACKGROUND: Adaptive laboratory evolution (ALE) is an impactful technique for cultivating microorganisms to adapt to specific environmental circumstances or substrates through iterative growth and selection. This study utilized an adaptive laboratory evolution method on Lipomyces starkeyi for high tolerance in producing lignin derivative alcohols and lipids from syringaldehyde. Afterward, untargeted metabolomics analysis was employed to find the key metabolites that play important roles in the better performance of evolved strains compared to the wild type. Lignin, a prominent constituent of plant biomass, is a favorable source material for the manufacture of biofuel and lipids. Nevertheless, the effective transformation of chemicals produced from lignin into products with high economic worth continues to be a difficult task. RESULTS: In this study, we exposed L. starkeyi to a series of flask passaging experiments while applying selective pressure to facilitate its adaptation to syringaldehyde, a specific type of lignin monomeric aldehyde. Using ALE, we successfully developed a new strain, DALE-22, which can synthesize syringyl alcohol up to 18.74 mM from 22.28 mM syringaldehyde with 41.9% lipid accumulation. In addition, a comprehensive examination of untargeted metabolomics identified six specific crucial metabolites linked to the improved tolerance of the evolved strain in the utilization of syringaldehyde, including 2-aminobutyric acid, allantoin, 4-hydroxyphenethyl alcohol, 2-aminoethanol, tryptophan, and 5-aminovaleric acid. CONCLUSION: The results of our study reveal how L. starkeyi adapts to using substrates produced from lignin. These findings offer important information for developing strategies to improve the process of converting lignin into valuable products for sustainable biorefinery applications.Oct. 2024, Microbial cell factories, 23(1) (1), 270 - 270, English, International magazine[Refereed]Scientific journal
- Oct. 2024, SynBio[Refereed][Invited]Scientific journal
- Aug. 2024, Engineering in Life Sciences[Refereed]Scientific journal
- Aug. 2024, Biochemical Engineering Journal[Refereed]Scientific journal
- Previously, we synthesized an evolved version of a bio-based polylactide (PLA) on microbial platforms using our engineered lactate-polymerizing enzyme (LPE). This lactate (LA)-based copolyester, LAHB, has advantages over PLA, including improved flexibility and biodegradability, and its properties can be regulated through the LA fraction. To expand the LA-incorporation capacity and improve polymer properties, in the state of in vivo LAHB production, propionyl-CoA transferases (PCTs) that exhibited enhanced production of LA-CoA than the conventional PCTs were selected. Here, the present study has demonstrated that the LA fraction of LAHB could be altered using various PCTs. Enhanced PCT performance was achieved by balancing polymer production and cell growth. Both events are governed by the use of acetyl-CoA, a commonly shared key metabolite. This could be attributed to the different reactivities of individual PCTs towards acetyl-CoA, which serves both as a CoA donor and a leading compound in the TCA cycle. Interestingly, we found complete sequence randomness in the LAHB copolymers, independent of the LA fraction. The mechanism of LA fraction-independent sequence randomness is discussed. This new PCT-based strategy synergistically combines with the evolution of LPE to advance the LAHB project, and enables us to perform advanced applications other than LAHB production utilizing CoA-linked substrates.Jun. 2024, International journal of biological macromolecules, 133055 - 133055, English, International magazine[Refereed]Scientific journal
- Only a few reports available about the assimilation of hydrophobic or oil-based feedstock as carbon sources by Lipomyces starkeyi. In this study, the ability of L. starkeyi to efficiently utilize free fatty acids (FFAs) and real biomass like palm acid oil (PAO) as well as crude palm kernel oil (CPKO) for growth and lipid production was investigated. PAO, CPKO, and FFAs were evaluated as sole carbon sources or in the mixed medium containing glucose. L. starkeyi was able to grow on the medium supplemented with PAO and FFAs, which contained long-chain length FAs and accumulated lipids up to 35% (w/w) of its dry cell weight. The highest lipid content and lipid concentration were achieved at 50% (w/w) and 10.1 g/L, respectively, when L. starkeyi was cultured in nitrogen-limited mineral medium (-NMM) supplemented with PAO emulsion. Hydrophobic substrate like PAO could be served as promising carbon source for L. starkeyi.May 2024, Journal of bioscience and bioengineering, 138(2) (2), 153 - 162, English, Domestic magazine[Refereed]Scientific journal
- Lead, Apr. 2024, Yeast[Refereed]Scientific journal
- Itaconic acid is a promising biochemical building block that can be used in polymer synthesis. Itaconic acid is currently produced in industry by the natural producer fungus Aspergillus terreus using glucose as a main carbon source. Most research for itaconic acid production using lignocellulosic-based carbon sources was carried out by A. terreus. Engineered Corynebacterium glutamicum strain which can grow in presence of fermentation inhibitors without effect on growth, was used for production of itaconic acid using sweet sorghum juice and bagasse sugar lysate (BSL). BSL contains many inhibitors unlike sorghum juice. C. glutamicum could grow in the media containing both types of lignocellulose-based carbon sources without showing any growth inhibition, however, sorghum juice was better in itaconic acid production than BSL. Different constructed strains of C. glutamicum were used for itaconic acid production, however, C. glutamicum ATCC 13032 pCH-Tad1optAdi1opt strain expressing Adi1/Tad1 genes (trans-pathway) from Ustilago maydis proved to be better in itaconic acid production giving final titer of 8.4 and 4.02 g/L using sweet sorghum juice and BSL as the sole carbon sources by fed-batch fermentation. Our study is the first for production of itaconic acid using sweet sorghum juice and BSL. The present study also proved that C. glutamicum can be used for enhancing itaconic acid production using lignocellulosic-based carbon sources.Jan. 2024, Enzyme and Microbial Technology, 172, 110345 - 110345, English, International magazine[Refereed]Scientific journal
- Dec. 2023, AIP Conference Proceedings, 2972(1) (1)[Refereed]International conference proceedings
- Lead, Nov. 2023, Biochemical Engineering Journal[Refereed]Scientific journal
- Plants produce sugars by photosynthesis and use them for growth and development. Sugars are transported from source-to-sink organs via the phloem in the vasculature. It is well known that vascular development is precisely controlled by plant hormones and peptide hormones. However, the role of sugars in the regulation of vascular development is poorly understood. In this study, we examined the effects of sugars on vascular cell differentiation using a vascular cell induction system named Vascular cell Induction culture System Using Arabidopsis Leaves (VISUAL). We found that sucrose has the strongest inhibitory effect on xylem differentiation among several types of sugars. Transcriptome analysis revealed that sucrose suppresses xylem and phloem differentiation from cambial cells. Physiological and genetic analysis suggested that sucrose might function through the BES1 transcription factor, which is the central regulator of vascular cell differentiation. Conditional overexpression of cytosolic invertase led to a decrease in the number of cambium layers due to an imbalance between cell division and differentiation. Taken together, our results suggest that sucrose potentially acts as a signal that integrates environmental conditions with the developmental program.May 2023, Plant & cell physiology, English, Domestic magazine[Refereed]Scientific journal
- Lignocellulose is resistant to degradation and requires pretreatment before hydrolytic enzymes can release fermentable sugars. Sulfuric acid has been widely used for biomass pretreatment, but high amount of degradation products usually occurred when using this method. To enhance accessibility to cellulose, we studied the performances of several dilute organic acid pretreatments of sugarcane bagasse and oil palm empty fruit bunch fiber. The results revealed that pretreatment with maleic acid yields the highest xylose and glucose release among other organic acids. The effects of concentration, duration of heating and heating temperature were further studied. Dilute maleic acid 1% (w/w) pretreatment at 180 °C was the key to its viability as a substitute for sulfuric acid. Moreover, maleic acid did not seem to highly promote the formation of either furfural or 5-HMF in the liquid hydrolysate after pretreatment.Nov. 2022, Bioresource technology, 369, 128382 - 128382, English, International magazine[Refereed][Invited]Scientific journal
- Oct. 2022, PROCESSES, 10(10) (10), English[Refereed][Invited]Scientific journal
- Acidic and chemical inhibitor stresses undermine efficient lactic acid bioproduction from lignocellulosic feedstock. Requisite coping treatments, such as detoxification and neutralizing agent supplementation, can be eliminated if a strong microbial host is employed in the process. Here, we exploited an originally robust yeast, Saccharomyces cerevisiae BTCC3, as a production platform for lactic acid. This wild-type strain exhibited a rapid cell growth in the presence of various chemical inhibitors compared to laboratory and industrial strains, namely BY4741 and Ethanol-red. Pathway engineering was performed on the strain by introducing an exogenous LDH gene after disrupting the PDC1 and PDC5 genes. Facilitated by this engineered strain, high cell density cultivation could generate lactic acid with productivity at 4.80 and 3.68 g L-1 h-1 under semi-neutralized and non-neutralized conditions, respectively. Those values were relatively higher compared to other studies. Cultivation using real lignocellulosic hydrolysate was conducted to assess the performance of this engineered strain. Non-neutralized fermentation using non-detoxified hydrolysate from sugarcane bagasse as a medium could produce lactic acid at 1.69 g L-1 h-1, which was competitive to the results from other reports that still included detoxification and neutralization steps in their experiments. This strategy could make the overall lactic acid bioproduction process simpler, greener, and more cost-efficient.Lead, Aug. 2022, Scientific reports, 12(1) (1), 13645 - 13645, English, International magazine[Refereed]Scientific journal
- When lignocellulosic biomass is utilized as a fermentative substrate to produce biochemicals, the existence of a yeast strain resistant to inhibitory chemical compounds (ICCs) released from the biomass becomes critical. To achieve the purpose, in this study, Saccharomyces yeast strains from a NBRC yeast culture collection were used for exploration and evaluated in two different media containing ICCs that mimic one another but resemble the hydrolysate of real biomass. Among them, S. cerevisiae F118 strain shows robustness upon the fermentation with unique flocculation trait that was strongly responsive to ICC stress. When this strain was cultured in the presence of ICCs, its cell wall hydrophobicity increased dramatically, and reduced significantly when the ICCs were depleted, demonstrating that cell-surface hydrophobicity can also act as an adaptive response to the ICCs. Cells from the strain with the highest cell-wall hydrophobicity displayed progressively stronger flocculation, indicating that the F118 strain is having unique robustness under ICC stress. Gene expression perturbation analysis revealed that mot3 gene encoding regulatory Mot3p from the F118 strain was expressed in response to the concentration of ICCs. This gene was found to control expression of ygp1 gene that encoding Ygp1p, one of cell wall proteins. Deep sequencing analysis revealed that the Mot3p of the F118 strain features a unique insertion and deletion of nucleotides that encode glutamine or asparagine residues, particularly in N-terminal domain, as determined by comparison to the Mot3p sequence from the S288c strain, which was employed as a control strain. Furthermore, the cell wall hydrophobicity of the S288c strain was greatly enhanced and became ICC-responsive after gene swapping with the mot3 gene from the F118 strain. The gene-swapped S288c strain fermented 6-fold faster than the wild-type strain, producing 14.5 g/L of ethanol from 30 g/L of glucose consumed within 24 h in a medium containing the ICCs. These such modifications to Mot3p in unique locations in its sequence have a potential to change the expression of a gene involved in cell wall hydrophobicity and boosted the flocculation response to ICC stress, allowing for the acquisition of extraordinary robustness.Lead, Mar. 2022, Metabolic engineering, 72, 82 - 96, English, International magazine[Refereed]Scientific journal
- Corresponding, Feb. 2022, PROCESSES, 10(2) (2), 269 - 269, English[Refereed]Scientific journal
- Each year, the palm oil industry generates a significant amount of biomass residue and effluent waste; both have been identified as significant sources of greenhouse gas (GHG) emissions. This issue poses a severe environmental challenge for the industry due to the possibility of long-term negative effects on human well-being. The palm-oil industry must invest significantly in the technology that is required to resolve these issues and to increase the industry's sustainability. However, current technologies for converting wastes such as lignocellulosic components and effluents into biochemical products are insufficient for optimal utilization. This review discusses the geographical availability of palm-oil biomass, its current utilization routes, and then recommends the development of technology for converting palm-oil biomass into value-added products through an integrated biorefinery strategy. Additionally, this review summarizes the palm oil industry's contribution to achieving sustainable development goals (SDGs) through a circular bioeconomy concept.Lead, Nov. 2021, Bioresource technology, 344(PB) (PB), 126266 - 126266, English, International magazine[Refereed]
- Lignocellulosic biomass has great potential as an inedible feedstock for bioplastic synthesis, although its use is still limited compared to current edible feedstocks of glucose and starch. This review focuses on recent advances in the production of biopolymers and biomonomers from lignocellulosic feedstocks with downstream processing and chemical polymer syntheses. In microbial production, four routes composed of existing poly (lactic acid) and polyhydroxyalkanoates (PHAs) and the emerging biomonomers of itaconic acid and aromatic compounds were presented to review present challenges and future perspectives, focusing on the use of lignocellulosic feedstocks. Recently, advances in purification technologies decreased the number of processes and their environmental burden. Additionally, the unique structures and high-performance of emerging lignocellulose-based bioplastics have expanded the possibilities for the use of bioplastics. The sequence of processes provides insight into the emerging technologies that are needed for the practical use of bioplastics made from lignocellulosic biomass.Oct. 2021, Bioresource technology, 344(PB) (PB), 126165 - 126165, English, International magazine[Refereed]
- Lead, May 2020, Processes, 8(5) (5), 619, English[Refereed]Scientific journal
- Lead, {MDPI} {AG}, Apr. 2020, Processes, 8(4) (4), 450 - 450, English[Refereed]Scientific journal
- Lead, Sep. 2019, Biochemical Engineering Journal, 149(15) (15), 107236, EnglishHigh cell density cultivation of Lipomyces starkeyi for achieving highly efficient lipid production from sugar under low C/N ratio[Refereed]
- Biorefinery has been suggested to provide relevant substitutes to a number of fossil products. Feedstocks and conversion technologies have, however, been the bottleneck to the realization of this concept. Herein, feedstocks and bioconversion technologies under biorefinery have been reviewed. Over the last decade, research has shown possibilities of generating tens of new products but only few industrial implementations. This is partly associated with low production yields and poor cost-competitiveness. This review addresses the technical barriers associated with the conversion of emerging feedstocks into chemicals and bioenergy platforms and summarizes the developed biotechnological approaches including advances in metabolic engineering. This summary further suggests possible future advances that would expand the portfolio of biorefinery and speed up the realization of biofuels and biochemicals.Lead, Jun. 2019, Biotechnology Journal, 14(6) (6), 1800494, English, International magazine[Refereed]Scientific journal
- Elsevier {BV}, Feb. 2019, Biochemical Engineering Journal, 142, 117 - 123, EnglishScientific journal
- A novel strategy for the low-cost, high-yield co-production of xylose and xylooligosaccharides together with no xylose inhibition was developed using a novel heterologous expression of XYN10Ks_480 endo-1,4-β-xylanase with a ricin-type β-trefoil type of domain and XYN11Ks_480 endo-1,4-β-xylanase with a CBM 2 superfamily from the Kitasatospora sp in an actinomycetes expression system. Xylose is the main building block for hemicellulose xylan. Our findings demonstrated high levels of expression and catalytic activity for XYN10Ks_480 during hydrolysis of the extracted xylan of bagasse, and three types of xylan-based substrates were used to produce xylose and xylooligosaccharides. However, hydrolysis by XYN11Ks_480 produced xylooligosaccharides without xylose formation. This study demonstrated how integrating sodium hypochlorite-extracted xylan and enzymatic hydrolysis could provide an alternative strategy for the generation of XOS from lignocellulosic material.Lead, Jan. 2019, Bioresource technology, 272, 315 - 325, English, International magazine[Refereed]Scientific journal
- The ability of oleaginous yeast Lipomyces starkeyi to efficiently produce lipids when cultivated on sap extracted from felled oil palm trunk (OPT) as a novel inexpensive renewable carbon source was evaluated. OPT sap was found to contain approximately 98 g/L glucose and 32 g/L fructose. Batch fermentations were performed using three different OPT sap medium conditions: regular sap, enriched sap, and enriched sap at pH 5.0. Under all sap medium conditions, the cell biomass and lipid production achieved were approximately 30 g/L and 60% (w/w), respectively. L. starkeyi tolerated acidified medium (initial pH ≈ 3) and produced considerable amounts of ethanol as well as xylitol as by-products. The fatty acid profile of L. starkeyi was remarkably similar to that of palm oil, one of the most common vegetable oil feedstock used in biodiesel production with oleic acid as the major fatty acid followed by palmitic, stearic and linoleic acids.Lead, Elsevier {BV}, Jan. 2019, Journal of bioscience and bioengineering, 127(6) (6), 726 - 731, English, Domestic magazine[Refereed]Scientific journal
- Springer Nature, Dec. 2018, Microbial Cell Factories, 17(1) (1), EnglishScientific journal
- Lead, Elsevier B.V., Sep. 2018, Biochemical Engineering Journal, 137, 182 - 191, English[Refereed]
- The aim of this study was to construct a cost-effective method for repeated bioethanol production using membrane (ultrafiltration permeation and nanofiltration concentration)-concentrated sweet sorghum juice by using flocculent Saccharomyces cerevisiae F118 strain. With low initial dry cell concentrations at around 0.28-0.35 g L-1, the S. cerevisiae F118 strain provided an ethanol titer of 86.19 ± 1.15 g L-1 (theoretical ethanol yield of 70.77%), which was higher than the non-flocculent S. cerevisiae BY4741 strain at 33.92 ± 0.99 g L-1 after 24 h fermentation. This result was correlated with higher gene expressions of the sucrose-hydrolysing enzyme invertase, sugar phosphorylation, and pyruvate-to-ethanol pathways in the F118 strain compared with the BY4741 strain. Sequential fed-batch fermentation was conducted, and the F118 strain was easily separated from the fermentation broth via the formation of flocs and sediment. After the 5th cycle of fermentation with the F118 strain, the ethanol concentration reached 100.37 g L-1.Lead, Jul. 2018, Bioresource technology, 265, 542 - 547, English, International magazine[Refereed]
- Actinobacteria plays a key role in the cycling of organic matter in soils. They secret biomass-degrading enzymes that allow it to produce the unique metabolites that originate in plant biomass. Although past studies have focused on these unique metabolites, a large-scale screening of Actinobacteria is yet to be reported to focus on their biomass-degrading ability. In the present study, a rapid and simple method is constructed for a large-scale screening, and the novel resources that form the plant biomass-degrading enzyme cocktail are identified from 850 isolates of Actinobacteria. As a result, Nonomuraea fastidiosa secretes a biomass degrading enzyme cocktail with the highest enzyme titer, although cellulase activities are lower than a commercially available enzyme. So the rich accessory enzymes are suggested to contribute to the high enzyme titer for a pretreated bagasse with a synergistic effect. Additionally, an optimized cultivation method of biomass induction caused to produce the improved enzyme cocktail indicated strong enzyme titers and a strong synergistic effect. Therefore, the novel enzyme cocktails are selected via the optimized method for large-scale screening, and then the enzyme cocktail can be improved via the optimized production with biomass-induction.Lead, Jul. 2018, Biotechnology journal, 14(3) (3), e1700744, English, International magazine[Refereed]Scientific journal
- Lead, Elsevier B.V., Jun. 2018, Journal of Bioscience and Bioengineering, 125(6) (6), 695 - 702, English[Refereed]Scientific journal
- Japan Society for Bioscience Biotechnology and Agrochemistry, 2018, Bioscience, Biotechnology and Biochemistry, 82(5) (5), 904 - 915, English[Refereed]Scientific journal
- Dec. 2017, BIORESOURCE TECHNOLOGY, 245(Pt B) (Pt B), 1400 - 1406, English[Refereed]
- Lead, Dec. 2017, BIORESOURCE TECHNOLOGY, 245(Pt B) (Pt B), 1436 - 1446, English[Refereed]Scientific journal
- Jul. 2017, APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 101(13) (13), 5279 - 5290, English[Refereed]Scientific journal
- May 2017, AMB EXPRESS, 7(1) (1), 100, English[Refereed]Scientific journal
- Mar. 2017, SCIENTIFIC REPORTS, 7, 43518, English[Refereed]Scientific journal
- Sep. 2016, BIOTECHNOLOGY FOR BIOFUELS, 9(1) (1), 188, English[Refereed]Scientific journal
- Apr. 2015, BIORESOURCE TECHNOLOGY, 182, 169 - 178, English[Refereed]Scientific journal
- Bioethanol production from lignocellulosic biomass, in particular xylose, is currently of great concern, given the abundance of this sugar in the world, because Saccharomyces cerevisiae, which is widely used for bioethanol production, is unable to naturally ferment xylose. The aim of this study was to obtain a novel yeast capable of stably producing ethanol from biomass containLead, Springer, 2014, Sustainable Chemical Processes, 2(17) (17), 1 - 12, English[Refereed]Scientific journal
- Dec. 2013, JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 116(6) (6), 725 - 733, English[Refereed]Scientific journal
- May 2011, JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 111(5) (5), 557 - 563, English[Refereed]Scientific journal
- Dec. 2010, POLYMER DEGRADATION AND STABILITY, 95(12) (12), 2250 - 2254, EnglishScientific journal
- Dec. 2010, Biosciences Biotechnology Research Asia, 7(2) (2), 617 - 622Scientific journal
- Lead, Nov. 2010, JOURNAL OF BIOTECHNOLOGY, 150, S136 - S137, English
- Oct. 2010, JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 110(4) (4), 453 - 458, English[Refereed]Scientific journal
- Lead, Jan. 2007, BIOPHYSICAL JOURNAL, -, 146A - 146A, EnglishOn the swiveling motion of helices of c-subunit in rotation of ATP synthase
- Polyhydroxyalkanoate (PHA) synthase (PhaC) from Wautersia eutropha was expressed in a wide range of production level in Escherichia coli XL1-Blue cells and its effects on PhaC activity, poly[(R)-3-hydroxybutyrate] [P(3HB)] production and its molecular weights were investigated. The production level of PhaC was controlled by both amount of chemical inducer (IPTG) added into the medium and use of different copy number of plasmids. In a flask experiment, as increasing PhaC production level in the cells, the PhaC activity also increased in the range of low PhaC concentration. However, PhaC activity did not further increase in the range of high PhaC concentration, probably due to formation of inclusion body in the cells. The molecular weight of P(3HB) was found to decrease with increasing PhaC activity. This trend was also verified in high cell density cultivation using 10-l jar fermentor. Furthermore, we demonstrated that use of low copy number plasmid and appropriate induction of PhaC expression were effective in achieving both high productivity and high molecular weight of P(3HB).Oct. 2006, Polymer Preprints, Japan, 55, 2204
- Aug. 2006, POLYMER DEGRADATION AND STABILITY, 91(8) (8), 1645 - 1650, EnglishScientific journal
- May 2006, POLYMER DEGRADATION AND STABILITY, 91(5) (5), 1138 - 1146, EnglishScientific journal
- Lead, 2006, BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 309 - 310, EnglishA crucial clue to understand the molecular rotation of c-subunit ring coupled with proton translocation through F(0) of thermophilic Bacillus PS3 ATP synthase
- 2005, Polymer Preprints, Japan, 54(1) (1), 2012, JapaneseEffect of PHA synthase activity and its concentration on the molecular weight of poly[(R)-3-hydroxybutyrate] synthesized in recombinant Escherichia coliInternational conference proceedings
- 2005, Polymer Preprints, Japan, 54(1) (1), 2014, JapaneseMolecular weight of poly[(R)-3-hydroxybutyrate] synthesized by type IV PHA synthase in Escherichia coli
- Lead, Jan. 2005, POLYMER DEGRADATION AND STABILITY, 87(1) (1), 161 - 169, EnglishScientific journal
- Lead, Jan. 2004, POLYMER DEGRADATION AND STABILITY, 83(1) (1), 79 - 86, EnglishScientific journal
- Jul. 2002, JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 94(1) (1), 29 - 33, English[Refereed]Scientific journal
- Jul. 2002, JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 94(1) (1), 29 - 33, English[Refereed]Scientific journal
- Lead, Mar. 2002, JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 93(3) (3), 274 - 280, English[Refereed]Scientific journal
- Epsilon-poly-L-lysine(以下ePL)は、アルカロイド生産菌の検索の過程で、Streptomyces albulusの生産するL-lysineのホモポリマー(n=25-30)として酒井らにより初めて見出されたePLは必須アミノ酸であるリジンのホモポリマーであるので安全性が高くかつカチオン含量が高いので、さらにHレタリー用品、食品添加物、化粧品、医寮晶、農薬晶、電子材料などの広範な用途が期待され、ePLの工業生産プロセスが重要になってくる。我々は、培養中のpHやグルコースの残存濃度などの培養条件を検討し、ePLの高収率生産プロセスを構築することを試みた。さらに、低コスト化に向けた高純度など一PL生産システムの構築を実現するためにエアリフト型バイオリアククーでの発酵生産を検討した。岐阜大学機関リポジトリ, 2002, 農学 甲第275号, English[Refereed]Doctoral thesis
- May 2001, JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 91(5) (5), 504 - 508, EnglishScientific journal
- Feb. 2001, JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 91(2) (2), 190 - 194, English[Refereed]Scientific journal
- Feb. 2001, JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 91(2) (2), 190 - 194, EnglishScientific journal
- Jun. 1999, JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 87(6) (6), 825 - 827, EnglishScientific journal
- Mar. 1999, JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 87(3) (3), 390 - 393, EnglishScientific journal
- 1997, JOURNAL OF FERMENTATION AND BIOENGINEERING, 84(2) (2), 176 - 178, EnglishScientific journal
- (公社)日本生物工学会, Aug. 2024, 日本生物工学会大会講演要旨集, 2024年, 83 - 83, JapaneseNovel method for simple antibody modification on nanoparticle surfaces using Spytag-Spycatcher system
- (公社)日本生物工学会, Aug. 2024, 日本生物工学会大会講演要旨集, 2024年, 83 - 83, JapaneseDevelopment of titanium peroxide nanoparticles using food ingredients and investigation of their cell-damaging effects
- (公社)日本生物工学会, Aug. 2024, 日本生物工学会大会講演要旨集, 2024年, 94 - 94, JapaneseDifferences between hyphae-aggregated type and hyphae-dispersed type of Aspergillus oryzae based on observations of cell organelles
- (公社)日本生物工学会, Aug. 2024, 日本生物工学会大会講演要旨集, 2024年, 94 - 94, English遺伝子組換え麹菌におけるイソプリメベロース生成酵素の産出に対する発酵パラメータの影響(Influence of fermentation parameter to the production of isoprimeverose-producing enzyme in genetically engineered Aspergillus oryzae)
- (公社)日本生物工学会, Aug. 2024, 日本生物工学会大会講演要旨集, 2024年, 94 - 94, JapaneseCulture characteristics of a filamentous fungus Aspergillus oryzae on different growth substrates including Sorghum juice
- (公社)日本生物工学会, Aug. 2024, 日本生物工学会大会講演要旨集, 2024年, 127 - 127, JapaneseHigh cell density cultures of S. cerevisiae using an improved MAXBLEND reactor
- (公社)日本生物工学会, Aug. 2024, 日本生物工学会大会講演要旨集, 2024年, 130 - 130, JapaneseConstruction and validation of a metabolic pathway model for thermophilic actinomycetes
- (公社)日本生物工学会, Aug. 2024, 日本生物工学会大会講演要旨集, 2024年, 130 - 130, JapaneseSecretory production of PETase by Streptomyces thermoviolaceus and its characterization
- (公社)日本生物工学会, Aug. 2024, 日本生物工学会大会講演要旨集, 2024年, 194 - 194, EnglishRalstonia eutrophaおよびその組換え株による種々の炭素源からのポリヒドロキシ酪酸(PHB)の生産(Production of poly-hydroxybutyrate(PHB) by Ralstonia eutropha and its recombinant strain from various carbon sources)
- (公社)日本生物工学会, Aug. 2024, 日本生物工学会大会講演要旨集, 2024年, 246 - 246, JapaneseEffect of pyruvate flux engineering on protein production in Aspergillus oryzae
- 2024, 日本生物工学会大会講演要旨集, 76thMicrobial production of lipids from various carbon sources by oleaginous yeast Lipomyces starkeyi
- 2024, 日本生物工学会大会講演要旨集, 76thDegradation and assimilation of Alcohol Maleate by esterase displaying yeast
- 2023, アグリバイオ, 7(6) (6)Current technologies for the utilization of grass biorefinery crops
- 2023, 日本農芸化学会西日本支部大会およびシンポジウム講演要旨集, 2023 (CD-ROM)S.cerevisiae BA11の耐性評価とキシロース資化性付与
- 2023, 日本生物工学会大会講演要旨集, 75thCharacterization of cultures with Saccharomyces yeast using MAXBLEND reactor
- 2023, 日本生物工学会大会講演要旨集, 75thPotential production of rare-disaccharide isoprimeverose by enzyme produced in Aspergillus oryzae
- 2023, 日本生物工学会大会講演要旨集, 75thElucidation of radio sensitizing mechanism of hydrogen peroxide using genome editing cells
- 2023, 化学とマイクロ・ナノシステム学会研究会講演要旨集(CD-ROM), 48th酵母の個体差の解析を目的とした空圧バルブ付きマイクロ流体デバイスの開発
- 2022, 日本生物工学会大会講演要旨集, 74thProduction of Biodegradable Plastics from Palm Industrial Waste as a Carbon Source by the Oleaginous Yeast Lipomyces starkeyi
- 2022, 日本生物工学会大会講演要旨集, 74thDevelopment of organic acid assimilating yeast and their application to bio-refineries from lignocellulosic biomass
- 2022, Program & Abstracts. Annual and International Meeting of the Japanese Association for Animal Cell Technology, 35th (CD-ROM)外来タンパク質を提示したインフルエンザVLPsの昆虫細胞を用いた生産
- 2022, 化学とマイクロ・ナノシステム学会研究会講演要旨集(CD-ROM), 46th酵母の個別解析のためのバルブ付きマイクロ流体デバイスの開発
- 2022, 日本生物工学会大会講演要旨集, 74thComparative analysis of metabolic strategies among various yeast species
- 2022, 化学工学会年会研究発表講演要旨集(CD-ROM), 87th異種タンパク質を提示するインフルエンザウイルス様粒子の昆虫細胞を用いた生産
- 2021, 化学工学会年会研究発表講演要旨集(CD-ROM), 86thパーム油産業廃棄物POMEを原料とする微生物による酵素・化学品への変換
- 2021, 日本生物工学会大会講演要旨集, 73rdBreeding of organic acid assimilation yeast for bio-refinery
- 2021, 日本生物工学会大会講演要旨集, 73rdPolyhydroxyalkanoic acid production by an oleaginous yeast strain Lipomyces starkeyi
- 2021, Program & Abstracts. Annual and International Meeting of the Japanese Association for Animal Cell Technology, 34thゲノム編集技術を用いた遺伝子組換え昆虫細胞の樹立
- 2021, 化学工学会秋季大会研究発表講演要旨集(CD-ROM), 52nd遺伝子組換え昆虫細胞樹立へのゲノム編集技術の応用
- 2019, 日本生物工学会大会講演要旨集, 71st酵母カルチャーコレクションからのバイオエタノール生産のための優良酵母の選抜と評価
- (公社)日本生物工学会, 2019, 日本生物工学会大会講演要旨集, 71st, 132 - 132, Japanese油脂酵母Lipomyces starkeyiの遺伝子的改変による長鎖長脂肪酸の生産
- (公社)日本生物工学会, Aug. 2018, 日本生物工学会大会講演要旨集, 平成30年度, 113 - 113, Japanese油脂酵母Lipomyces starkeyiD35株の繰り返し発酵による脂肪酸組成変化解析
- 2018, 日本農芸化学会大会講演要旨集(Web), 2018Saccharomyces cerevisiae酵母におけるCandida boidinii由来キシロース発酵代謝系の導入効果
- 2018, 日本生物工学会大会講演要旨集, 70thThe enhancement of culture conditions for high cell and lipid production of oleaginous yeast Lipomyces starkeyii D35
- 2018, 日本生物工学会大会講演要旨集, 70thバイオマス分解酵素の大規模スクリーニングで見出した希少放線菌
- 2017, 日本生物工学会大会講演要旨集, 69thExploration of potential indigenous marine actinomycetes from indonesia soil producing enzyme lignocellulosic for biorefinery application
- 2017, 日本生物工学会大会講演要旨集, 69thThe establishment high cell density culture of oleaginous Lipomyces starkeyi D35 for high cell and lipid production
- 2017, 日本生物工学会大会講演要旨集, 69thHigh Production of single cell oil from glucose and xylose using oleaginous yeast Lipomyces starkeyi
- 2017, 日本生物工学会大会講演要旨集, 69th発酵阻害耐性酵母由来強力なENO1プロモーターの発現解析
- 2017, 日本生物工学会大会講演要旨集, 69th発酵阻害物質耐性Candida boidinii K212のキシロース発酵の解析
- Sep. 2016, BIOTECHNOLOGY FOR BIOFUELS, 9(Sept) (Sept), 9:188 (WEB ONLY), English
- 25 Aug. 2016, 日本生物工学会大会講演要旨集, 68th, 316, Japanese凝集性酵母における新規な阻害剤耐性機構の解明
- 13 Mar. 2016, 化学工学会年会研究発表講演要旨集(CD-ROM), 81st, ROMBUNNO.N316, EnglishYeast breeding for fuels and chemicals production from Indonesia Culture Collection
- 13 Mar. 2016, 化学工学会年会研究発表講演要旨集(CD-ROM), 81st, ROMBUNNO.N321, EnglishEconomic Value of Current Main Use of Oil Palm Empty Fruit Bunches (EFB) and Its Potential Use for Biofuel
- 13 Mar. 2016, 化学工学会年会研究発表講演要旨集(CD-ROM), 81st, ROMBUNNO.N302, EnglishBiorefinery research in Kobe and Indonesia
- 13 Mar. 2016, 化学工学会年会研究発表講演要旨集(CD-ROM), 81st, ROMBUNNO.N313, EnglishBiorefinery as strategic approach for supporting of utilization of tropical lignocellulosic biomas
- 05 Mar. 2016, 日本農芸化学会大会講演要旨集(Web), 2016, 4A022 (WEB ONLY), Japaneseマンナンバイオマスからのエタノール生産:β‐マンナナーゼとβ‐マンノシダーゼを細胞表層に提示した出芽酵母の開発
- 07 Sep. 2015, 日本放線菌学会大会講演要旨集, 30th, 105, Japaneseインドネシアの土壌から分離された放線菌由来マンナナーゼ酵素の単離と酵素活性評価
- 05 Mar. 2015, 日本農芸化学会大会講演要旨集(Web), 2015, 3B33A01 (WEB ONLY), Japanese実バイオマスを微生物変換するための新しい酵母プラットフォームの探索
- 2015, 日本ゲノム微生物学会年会要旨集, 9th実バイオマスからエタノール発酵するための酵母株の探索
- 2015, 化学工学会大会講演要旨集(CD-ROM), 2015インドネシアを例としたバイオコンビナート構想
- The Society for Biotechnology, Japan, 25 Aug. 2013, 日本生物工学会大会講演要旨集, 65, 137 - 137, Japanese2P-132 Production of low-temperature cellulase by Trichoderma reesei mutant
- 2013, 日本農芸化学会大会講演要旨集(Web), 2013キシロース発酵における細胞融合酵母FSC株のin vitro代謝解析
- The Society for Biotechnology, Japan, 25 Sep. 2012, 日本生物工学会大会講演要旨集, 64, 240 - 240, English4Ia05 Synergistic effect of delignification and alkaline swelling treatments on enzymatic degradation of rice straw
- 2012, 日本農芸化学会大会講演要旨集(Web), 2012稲わらの並行復発酵ための高活性セルラーゼ生産
- The Society for Biotechnology, Japan, 25 Aug. 2011, 日本生物工学会大会講演要旨集, 63, 109 - 109, Japanese2Aa02 Xylose-fermenting yeast developed by mutation-fusion technique for bioethanol production
- 2011, 日本農芸化学会大会講演要旨集, 2011高効率エタノール変換に向けた稲藁の脱リグニン及び弛緩処理技術の開発
- The Society for Biotechnology, Japan, 25 Sep. 2010, 日本生物工学会大会講演要旨集, 22, 55 - 55, Japanese2P-1185 Enhancement of xylose uptake in Saccharomyces cerevisiae by EMS mutagenesis
- The Society for Biotechnology, Japan, 25 Aug. 2009, 日本生物工学会大会講演要旨集, 21, 106 - 106, Japanese2Ha04 High efficient biomass conversion of unused agricultural residues to bioethanol
- The Society for Biotechnology, Japan, 03 Aug. 2006, 日本生物工学会大会講演要旨集, 18, 176 - 176, Japanese1J14-5 Effect of PHA synthase activity on polyester molecular weight
- 2006, 高分子学会予稿集(CD-ROM), 55(1 Disk1) (1 Disk1)遺伝子組換え大腸菌が合成するポリ[(R)-3-ヒドロキシブタン酸]の分子量
- 2006, 生化学INSIGHT INTO THE MOLECULAR ROTATION OF C-SUBUNIT RING IN THERMOPHILIC BACILLUS PS3 ATP SYNTHASE
- The Biophysical Society of Japan General Incorporated Association, 2006, Seibutsu Butsuri, 46(2) (2), S350, English
- 2005, 高分子学会予稿集(CD-ROM), 54(1 Disk1) (1 Disk1)ポリ(3-ヒドロキシブチレート)の分子量における重合酵素の発現量および酵素活性の影響
- 2005, 高分子学会予稿集(CD-ROM), 54(2 Disk1) (2 Disk1)Effect of temperature on molecular weight of poly[(R)-3-hydroxybutyrate)] synthesized by Bacillus sp. INT005 PHA synthase in recombinant Escherichia coli
- The Society for Biotechnology, Japan, 25 Aug. 2004, 日本生物工学会大会講演要旨集, 16, 156 - 156, Japanese2D14-1 Production of polyhydroxyalkanoate copolymer from soybean oil and its LCI analysis
- 2004, 高分子学会予稿集(CD-ROM), 53(2 Disk1) (2 Disk1)Factors affecting the molecular weight of poly[(R)-3-hydroxybutyrate] in recombinant Escherichia coli
- 2004, 高分子学会予稿集(CD-ROM), 53(1) (1)遺伝子組換え大腸菌による超高分子量P(3HB)の効率的生産
- 2004, 高分子学会予稿集(CD-ROM), 53(2 Disk1) (2 Disk1)遺伝子組換え微生物を用いたポリヒドロキシアルカン酸(PHA)の効率的生合成手法の開発
- 2003, 高分子学会予稿集, 52(5) (5)大豆油を原料としたバイオポリエステルの高効率・高収率生産
- 2003, 高分子学会予稿集, 52(14) (14)バイオポリエステル微生物生産とライフサイクルインベントリ評価
- Feb. 2001, JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 91(2) (2), 190 - 194, EnglishEnhancement of epsilon-polylysine production by Streptomyces albulus strain 410 using pH control
- 01 Dec. 2000, 日本農芸化学会誌, 74(12) (12), 1399, Japanese放線菌Streptomyces therotoleransによる基質タロシンからアセチルイソバレリルタイロシン(AIV)への微生物交換プロセスにおける基質流加速度の最適化
- The Society for Biotechnology, Japan, 16 Aug. 1999, 日本生物工学会大会講演要旨集, 11, 228 - 228, JapaneseEffect of Soybean Oil on Production of Antibiotics
- 公益社団法人日本生物工学会, 16 Aug. 1999, 日本生物工学会大会講演要旨集, 11, 225 - 225, Japanese1029 3-アセチル-4"-イソバレリルタイロシン(AIV)生産における動力学モデルの作成
- The Society for Biotechnology, Japan, 16 Aug. 1999, 日本生物工学会大会講演要旨集, 11, 218 - 218, JapaneseSTUDY ON THE MICROBIAL PRODUCTION OF ε-POLYLYSINE IN AN AIRLIFT BIOREACTOR
- The Society for Biotechnology, Japan, 31 Aug. 1998, 日本生物工学会大会講演要旨集, 10, 215 - 215, JapaneseStudy on Enhanced Microbial Production of εPL by Streptomyces albulus No.410
- Joint work, Important key points regarding the circular bioeconomy in the palm oil industry, Routledge, Mar. 2025, ISBN: 103285541XThe Palm Oil Export Market: Trends, Challenges, and Future Strategies for Sustainability (Routledge Studies in the Economics of Business and Industry)
- Ethanol Production by Recombinant CBP Yeasts, Springer, Dordrecht, Nov. 2024, ISBN: 9400763077Handbook of Biorefinery Research and Technology
- Joint work, Advanced Lignin Valorization for Biorefinery Application, Intechopen, Jul. 2024, ISBN: 0854667644Advanced Lignin Technologies
- Joint work, Agriculturak Biotechnology, Jun. 2023Current technologies for the utilization of grass biorefinery crops
- Single work, Synergistic Effects of Pretreatment Process on Enzymatic Digestion of Rice Straw for Efficient Ethanol Fermentation, Intechopen, Feb. 2013, ISBN: 9789535109723Environmental Biotechnology: New Approaches and Prospective Applications
- 第19回化学工学会学生発表会, Mar. 2017, Japanese, 化学工学会関西支部, 豊中市, Domestic conferenceREDOXバランスにおける発酵阻害耐性酵母由来新規TDHxの影響Oral presentation
- Metabolic Engineering 11, Jun. 2016, English, Metabolic Engineering 11, 淡路市, International conferenceDevelopment of Platform Yeast Strain Capable of Direct Fermentation of Raw Biomass to EthanolOral presentation
- 化学工学会年会研究発表講演要旨集(CD-ROM), Mar. 2016, EnglishYeast breeding for fuels and chemicals production from Indonesia Culture Collection
- 化学工学会年会研究発表講演要旨集(CD-ROM), Mar. 2016, EnglishEconomic Value of Current Main Use of Oil Palm Empty Fruit Bunches (EFB) and Its Potential Use for Biofuel
- 化学工学会年会研究発表講演要旨集(CD-ROM), Mar. 2016, EnglishBiorefinery research in Kobe and Indonesia
- 化学工学会年会研究発表講演要旨集(CD-ROM), Mar. 2016, EnglishBiorefinery as strategic approach for supporting of utilization of tropical lignocellulosic biomas
- 日本農芸化学会2016年度大会, Mar. 2016, Japanese, Domestic conferenceマンナンバイオマスからのエタノール生産:βーマンナナーゼとβーマンノシダーゼを細胞表層に提示した出芽酵母の開発Oral presentation
- 日本放線菌学会大会講演要旨集, Sep. 2015, Japaneseインドネシアの土壌から分離された放線菌由来マンナナーゼ酵素の単離と酵素活性評価
- 日本農芸化学会大会講演要旨集(Web), Mar. 2015, Japanese実バイオマスを微生物変換するための新しい酵母プラットフォームの探索
- 日本農芸化学会2015年度大会, Mar. 2015, Japanese, 日本農芸化学会, 岡山市, Domestic conference実バイオマスを微生物変換するための新しい酵母プラットフォームの探索Oral presentation
- 日本ゲノム微生物学会年会要旨集, 2015, Japanese実バイオマスからエタノール発酵するための酵母株の探索
- 化学工学会大会講演要旨集(CD-ROM), 2015, Japaneseインドネシアを例としたバイオコンビナート構想
- 日本生物工学会大会講演要旨集, Aug. 2013, JapaneseTrichoderma reesei変異菌による低温性セルラーゼの産生
- 日本農芸化学会大会講演要旨集(Web), Mar. 2013, Japaneseキシロース発酵における細胞融合酵母FSC株のin vitro代謝解析
- 日本生物工学会大会講演要旨集, Sep. 2012, EnglishSynergistic effect of delignification and alkaline swelling treatments on enzymatic degradation of rice straw
- 日本農芸化学会大会講演要旨集(Web), Mar. 2012, Japanese稲わらの並行復発酵ための高活性セルラーゼ生産
- 日本生物工学会大会講演要旨集, Aug. 2011, Japaneseバイオエタノール生産ための細胞変異融合法によるキシロース代謝利用酵母の分子育種
- 日本農芸化学会大会講演要旨集, Mar. 2011, Japanese高効率エタノール変換に向けた稲藁の脱リグニン及び弛緩処理技術の開発
- 日本生物工学会大会講演要旨集, Sep. 2010, JapaneseEMS変処理によるサカロマイセス酵母のキシロース取込能力の強化
- 日本生物工学会大会講演要旨集, Aug. 2009, Japanese未利用農業廃棄物からバイオエタノールへの効率的変換
- 高分子学会予稿集(CD-ROM), Sep. 2007, Japanese微生物合成ポリエステルの分子量特性
- 生物物理, Oct. 2006, EnglishInsigh into The molecular rotation of c-subunit ring in Thermophilic Bacillus PS3 ATP synthase
- Biophysics, Oct. 2006, English2P220 Insigh into The molecular rotation of c-subunit ring in Thermophilic Bacillus PS3 ATP synthase(37. Molecular motor (II),Poster Session,Abstract,Meeting Program of EABS & BSJ 2006)
- 日本生物工学会大会講演要旨集, Aug. 2006, JapanesePHA合成酵素活性がポリ[(R)‐3‐ヒドロキシブタン酸]の分子量に及ぼす影響
- 高分子学会予稿集(CD-ROM), May 2006, Japanese遺伝子組換え大腸菌が合成するポリ[(R)‐3‐ヒドロキシブタン酸]の分子量
- 生化学, 2006, EnglishINSIGHT INTO THE MOLECULAR ROTATION OF C-SUBUNIT RING IN THERMOPHILIC BACILLUS PS3 ATP SYNTHASE
- Polymer Preprints, Japan, Dec. 2005, In this study, we investigated the molecular weight of P(3HB) synthesized by the type IV PHA synthase from Bacillus sp. INT005 (PhaRC Bs). The PhaRC Bs preferred to synthesize low molecular weight of P(3HB) in Escherichia coli. The curve of molecular weight distribution was found to depend on cultivation time. Host strain of E. coli also affected the molecular weight of polymer, but culture temperature did not.Molecular weight of poly[(R)-3-hydroxybutyrate] synthesized by type IV PHA synthase in Escherichia coli
- 高分子学会予稿集(CD-ROM), Sep. 2005, EnglishEffect of temperature on molecular weight of poly[(R)-3-hydroxybutyrate)] synthesized by Bacillus sp. INT005 PHA synthase in recombinant Escherichia coli
- 高分子学会予稿集(CD-ROM), May 2005, Japaneseポリ(3‐ヒドロキシブチレート)の分子量における重合酵素の発現量および酵素活性の影響
- 高分子学会予稿集(CD-ROM), May 2005, EnglishMolecular weight of poly[(R)-3-hydroxybutyrate] synthesized by type IV PHA synthase in Escherichia coli
- 高分子学会予稿集(CD-ROM), Sep. 2004, Japanese遺伝子組換え微生物を用いたポリヒドロキシアルカン酸(PHA)の効率的生合成手法の開発
- 高分子学会予稿集(CD-ROM), Sep. 2004, EnglishFactors affecting the molecular weight of poly[(R)-3-hydroxybutyrate] in recombinant Escherichia coli
- 日本生物工学会大会講演要旨集, Aug. 2004, Japanese大豆油からのバイオポリエステル生産と環境影響評価
- 高分子学会予稿集(CD-ROM), May 2004, Japanese遺伝子組換え大腸菌による超高分子量P(3HB)の効率的生産
- 第56回日本生物工学会大会, 2004, Japanese, 日本生物工学会, 名城大学、名古屋市, Domestic conference大豆油からのバイオポリエステル生産と環境影響評価Oral presentation
- Int. Symposium on Biological Polyesters, 2004, English, IUPAC, Beijing, China, International conferenceEffective Production and Kinetic Characteristic of Ultra-high-molecular-weight of PHB in Recombinant Escherichia coli.Poster presentation
- 高分子学会予稿集, Sep. 2003, Japaneseバイオポリエステル微生物生産とライフサイクルインベントリ評価
- 高分子学会予稿集, May 2003, Japanese大豆油を原料としたバイオポリエステルの高効率・高収率生産
- 日本農芸化学会大会講演要旨集, Mar. 2002, Japaneseエアリフト型バイオリアクター(Airlift Bioreactor,ABR)におけるε‐ポリリジン(ε‐Polylysine,ε‐PL)の生産に関する研究
- 乳酸菌工学研究部会講演会, 2002, Japanese, 日本生物工学会, 茨城, Domestic conference有限要素法による気泡塔における溶存酸素分布の解析[Invited]Invited oral presentation
- 日本農芸化学会誌, Dec. 2000, Japanese放線菌Streptomyces therotoleransによる基質タロシンからアセチルイソバレリルタイロシン(AIV)への微生物交換プロセスにおける基質流加速度の最適化
- 化学工学会秋季大会研究発表講演要旨集, Aug. 2000, Japaneseエアリフト型バイオリアクターを用いた培養系における溶存酸素濃度の時間的分布の解析
- The 11th International Biotechnology Symposium, 2000, English, IUPAC, Berlin, Germany, International conferenceProduction of epsilon-polylysine by Streptomyces albulus Strain.Poster presentation
- 日本生物工学会大会講演要旨集, Aug. 1999, Japanese抗生物質生産への大豆油の効果について
- 日本生物工学会大会講演要旨集, Aug. 1999, Japaneseエアリフト型バイオリアクターでのε‐ポリリジン(PL)の発酵生産に関する研究
- 日本生物工学会大会講演要旨集, Aug. 1999, Japanese3‐アセチル‐4′′‐イソバレリルタイロシン(AIV)生産における動力学モデルの成
- 日本生物工学会大会講演要旨集, Aug. 1999, JapaneseEffect of Soybean Oil on Production of Antibiotics
- 日本生物工学会大会講演要旨集, Aug. 1999, Japanese1029 3-アセチル-4"-イソバレリルタイロシン(AIV)生産における動力学モデルの作成
- 日本生物工学会大会講演要旨集, Aug. 1999, JapaneseSTUDY ON THE MICROBIAL PRODUCTION OF ε-POLYLYSINE IN AN AIRLIFT BIOREACTOR
- 日本生物工学会大会講演要旨集, Aug. 1998, JapaneseStudy on Enhanced Microbial Production of εPL by Streptomyces albulus No.410
- 日本生物工学会大会講演要旨集, 1998, JapaneseStudy on Enhanced Microbial Production of .EPSILON.PL by Streptomyces albulus No.410.
- 日本化学工学会Jan. 2023 - Present
- 日本高分子学会Apr. 2002 - Present
- 日本農芸化学会Apr. 1996 - Present
- 日本生物工学会Apr. 1996 - Present
- Fujimori Science and Technology Foundation, Research Grand, Apr. 2023 - Mar. 2024, Principal investigatorProduction and Diversification of High Purity Poly(lactic acid) based Polymer by Robust Yeast
- 学術研究助成基金助成金/基盤研究(C), Apr. 2016 - Mar. 2019, Principal investigatorCompetitive research funding
■ Academic Contribution Activities