松田研究室
Matsuda Laboratory

since 2004

東京科学大学（旧東京工業大学）｜ Institute of Science Tokyo (prev. Tokyo Institute of Technology)
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Future Directions in Biocatalysis, 2nd edition
T. Matsuda, Ed. Elsevier
 was just published.
I appreciate very much the contributions of many excellent chapters.
2017.8.15に出版されました。
ご執筆していただいた皆様
非常に興味深い原稿をいただき、誠に有難うございました。


Papers


67 Highly enantioselective reduction of benzophenones by engineered Geotrichum candidum alcohol dehydrogenase
Z. Tang, G. G. Otárola Tejada, A. A. Koesoema, T. Matsuda Appl. Microbiol. Biotechnol. 2026, 110, 48. doi.org/10.1007/s00253-026-13717-0

66 Substrate expansion of Geotrichum candidum alcohol dehydrogenase towards diaryl ketones by mutation
Z. Tang, Y. Takagi, A. A. Koesoema, T. Matsuda Appl. Microbiol. Biotechnol. 2024, 108, 545. doi.org/10.1007/s00253-024-13375-0

65 Substrate Promiscuity of Thermoplasma acidophilum Malic Enzyme for CO2 Fixation Reaction
Y. Oku and T. Matsuda, JACS Au, 2024, 4, 1758－1762. doi.org/10.1021/jacsau.4c00290

64 Sustainable approach for highly-enantioselective synthesis of lactones by a Baeyer-Villiger Monooxygenase from Fusarium
L. H. L. Viet, M. Tamura, T. Matsuda, Tetrahedron, 2024, 154, 133875. doi.org/10.1016/j.tet.2024.133875

63 Immobilization of Thermoplasma acidophilum glucose dehydrogenase and isocitrate dehydrogenase through enzyme-inorganic hybrid nanocrystal formation
S. Oshima, Y. Oku, K. T.sriwong, Y. Kimura, T. Matsuda, Curr. Microbiol. 2024, 81, 67. doi.org/10.1007/s00284-023-03577-6

62 Enzyme immobilization on 3D-printed reactor for aldehyde oxidation to carboxylic acid under mild conditions
K. Nakahara, K. T.sriwong, M. A. Hawari, A. Tanaka, T. Matsuda, React. Chem. Eng. 2023, 8, 543-547. doi.org/10.1039/D2RE00547F

61 Asymmetric synthesis of sulfoxides by novel Baeyer-Villiger monooxygenase from Fusarium
L. H. L. Viet, H. Nemoto, M. Tamura, T. Matsuda, Tetrahedron, 2023, 131, 133204. doi.org/10.1016/j.tet.2022.133204

60 The protein-stabilizing effects of TMAO in aqueous and non-aqueous conditions
H. Monhemi, H. N. Hoang, D. M. Standley, T. Matsuda, M. R. Housaindokht
Phys. Chem. Chem. Phys. 2022, 24, 21178-21187.

59 Rate enhancement of lipase-catalyzed reaction using CO2-expanded liquids as solvents for chiral tetralol synthesis
Y. Suzuki, K. Taniguchi, H. N. Hoang, M. Tamura, T. Matsuda
Tetrahedron Lett. 2022, 153837.

58 Facile mussel-inspired polydopamine-coated 3D-printed bioreactors for continuous flow biocatalysis
K. T.sriwong, T. Matsuda
React. Chem. Eng. 2022, 7, 1053－1060.

57 Immobilization of Baeyer-Villiger monooxygenase from acetone grown Fusarium sp.
M. Takagi, K. T.sriwong, A. Masuda, N. Kawaguchi, S. Fukui, H. L. V. Lan, D. Kato, T. Kitayama, M. Fujii, A. A. Koesoema, T. Matsuda
Biotech. Lett. 2022, 44, 461－471.

56 Geotrichum candidum acetophenone reductase immobilization on reduced graphene oxide: a promising biocatalyst for green asymmetric reduction of ketones
K. T.sriwong, R. Kamogawa, C. S. C. Issasi, M. Sasaki, T. Matsuda
Biochem. Eng. J. 2022, 177, 108263.

55 Geotrichum candidum aldehyde dehydrogenase-inorganic nanocrystal with enhanced activity
K. T.sriwong, K. Ogura, M. A. Hawari, T. Matsuda
Enzyme Microb. Technol. 2021, 150, 109866.

54 Enzymatic direct carboxylation under supercritical CO2
K. R. A. Are, S. Ohshima, Y. Koike, Y. Asanuma, S. Kashikura, M. Tamura, T. Matsuda
Biochem. Eng. J. 2021, 171, 108004.

53 CO2-expanded liquids as solvents to enhance activity of Pseudozyma antarctica lipase B towards ortho-substituted 1-phenylethanols
M. Otsu, Y. Suzuki, A. A. Koesoema, H. N. Hoang, M. Tamura, T. Matsuda
Tetrahedron Lett. 2020, 61, 152424.

52 Organic-inorganic nanocrystal reductase to promote green asymmetric synthesis
K. T.sriwong, A. A. Koesoema, T. Matsuda
RSC Advances, 2020, 10, 30953－30960.

51 Oxidation of aromatic and aliphatic aldehydes to carboxylic acids by Geotrichum candidum aldehyde dehydrogenase
T. Hoshino, E. Yamabe, M. A. Hawari, M. Tamura, S. Kanamaru, K. Yoshida, A. A. Koesoema, T. Matsuda
Tetrahedron. 2020, 76, 131387.

50 Control of enantioselectivity in the enzymatic reduction of halogenated acetophenone analogs by substituent positions and sizes
A. A. Koesoema, D. M. Standley, S. Ohshima, M. Tamura, T. Matsuda
Tetrahedron Lett. 2020, 61, 151820.

49 Access to both enantiomers of substituted 2-tetralol analogs by a highly enantioselective reductase
A. A. Koesoema, D. M. Standley, K. T.Sriwong, M. Tamura, T. Matsuda
Tetrahedron Lett. 2020, 61, 151682.

48 Reversible control of enantioselectivity by the length of ketone substituent in biocatalytic reduction
A. A. Koesoema, Y. Sugiyama, K. T.Sriwong, Z. Xu, S. Verina, D. M. Standley, M. Senda, T. Senda, T. Matsuda
Appl. Microbiol. Biotechnol. 2019, 103, 9529-9541.

47 Structural basis for a highly (S)-enantioselective reductase towards aliphatic ketones with only one carbon difference between side chain
A. A. Koesoema, Y. Sugiyama, Z. Xu, D. M. Standley, M. Senda, T. Senda, T. Matsuda
Appl. Microbiol. Biotechnol. 2019, 103, 9543-9553.

46 Modulating biocatalytic activity toward sterically bulky substrates in CO2-expanded biobased liquids by tuning the physicochemical properties
H. N. Hoang, E. Granero-Fernandez, S. Yamada, S. Mori, H. Kagechika, Y. Medina-Gonzalez, T. Matsuda
ACS Sustainable Chem. Eng., 2017, 5, 11051-11059. DOI: 10.1021/acssuschemeng.7b03018

45 CO2-expanded bio-based liquids as novel solvents for enantioselective biocatalysis
H. N. Hoang, Y. Nagashima, S. Mori, H. Kagechika, T. Matsuda
Tetrahedron 2017, 73, 2984-2989. http://dx.doi.org/10.1016/j.tet.2017.04.024

44 Expanding substrate scope of lipase-catalyzed transesterification by the utilization of liquid carbon dioxide
H. N. Hoang, T. Matsuda
Tetrahedron 2016, 72, 7229-7234. http://dx.doi.org/10.1016/j.tet.2015.11.052.

43 Crystallization and preliminary crystallographic analysis of acetophenone reductase from Geotrichum candidum NBRC 4597
Y. Sugiyama, M. Senda, T. Senda, T. Matsuda
Acta Crystallogr. F71, 2015, 320-323. doi:10.1107/S2053230X15002265.

42 Liquid carbon dioxide as an effective solvent for immobilized Candida antarctica lipase B catalyzed transesterification
H. N. Hoang, T. Matsuda
Tetrahedron Lett. 2015, 56, 639-641.

41 Acetophenone reductase with extreme stability against a high concentration of organic compounds or an elevated temperature
T. Yamamoto, Y. Nakata, C. Cao, Y. Sugiyama, Y. Asanuma, S. Kanamaru, T. Matsuda
Appl. Microbiol. Biotechnol. 2013, 97, 10413-10421. DOI: 10.1007/s00253-013-4801-5

40 Purification and characterization of fluorinated ketone reductase from Geotrichum candidum NBRC 5767
C. Cao, T. Fukae, T. Yamamoto, S. Kanamaru, T. Matsuda
Biochem. Eng. J. 2013, 76, 13-16. DOI: 10.1016/j.bej.2013.04.005

39 Reduction of acetophenones with methyl fluorines and a bulky group on the aromatic ring using microorganisms and related enzymes
C. Abe, T. Sugawara, T. Machida, T. Higashi, K. Hanaya, M. Shoji, C. Cao, T. Yamamoto, T. Matsuda, T. Sugai
J. Mol. Catal. B: Enzym. 2012, 82, 86-91.

38 Stabilization of pyruvate decarboxylase under pressurized carbon dioxide and water biphasic system
T. Matsuda, K. Nakayama, T. Abe, M. Mukouyama
Biocatal. Biotrans. 2010, 28, 167-171.DOI: 10.3109/10242421003734696

37 Transesterification of supercritical ethyl acetate by higher alcohol
M. Fusayasu, T. Kamitanaka, T. Sunamura, T. Matsuda, T. Osawa, T. Harada
J. Supercritical Fluids, 2010, 54, 231-236.

36 Ring-methylation of pyrrole and indole using supercritical methanol
N. Kishida, T. Kamitanaka, M. Fusayasu, T. Sunamura, T. Matsuda, T. Osawa, T. Harada
Tetrahedron, 2010, 66, 5059-5064.

35 Purification and characterization of acetophenone reductase with excellent enantioselectivity from Geotrichum candidum NBRC 4597
Y. Nakata, T. Fukae, R. Kanamori, S. Kanamaru, T. Matsuda
Appl. Microbiol. Biotechnol. 2010, 86, 625-631.

34 A novel method for enzymatic asymmetric reduction of ketones in a supercritical carbon dioxide / water biphasic system
T. Harada, Y. Kubota, T. Kamitanaka, K. Nakamura, T. Matsuda
Tetrahedron Lett. 2009, 50, 4934-4936.

33 The Meerwein-Ponndorf-Verley-Oppenauer type reaction in supercritical or high-temperature alcohols or acetone without catalyst: effect of oxidation enthalpy and solvent concentrations on yield
T. Kamitanaka, Y. Ono, H. Morishima, T. Hikida, T. Matsuda, T. Harada
J. Supercritical Fluids, 2009, 49, 221-226.

32 Utility of ionic liquid for Geotrichum candidum-catalyzed synthesis of optically active alcohols
T. Tanaka, N. Iwai, T. Matsuda, T. Kitazume
J. Mol. Catal. B: Enz. 2009, 57, 317-320.

31 Asymmetric reduction of ketones by Geotrichum candidum: immobilization and application to reactions using supercritical carbon dioxide
T. Matsuda, R. Marukado, M. Mukouyama, T. Harada, K. Nakamura
Tetrahedron: Asymmetry, 2008, 19, 2272-2275.

30 Novel Continuous Carboxylation Using Pressurized Carbon Dioxide by Immobilized Decarboxylase
T. Matsuda, R. Marukado, S. Koguchi, T. Nagasawa, M. Mukouyama, T. Harada, K. Nakamura
Tetrahedron Lett. 2008, 49, 6019-6020.

29 Transformation of benzonitrile into benzyl alcohol and benzoate esters in supercritical alcohols
T. Kamitanaka, K. Yamamoto, T. Matsuda, T. Harada
Tetrahedron, 2008, 64, 5699-5702.

28 Direct addition of supercritical alcohols, acetone or acetonitrile to the alkenes without catalysts
T. Kamitanaka, T. Hikida, S. Hayashi, N. Kishida, T. Matsuda, T. Harada
Tetrahedron Lett. 2007, 48, 8460-8463.

27 Mechanism for the reduction of ketones to the corresponding alcohols using supercritical 2-propanol
T. Kamitanaka, T. Matsuda, T. Harada
Tetrahedron, 2007, 63, 1429-1434.

26 An effective method to use ionic liquids as reaction media for asymmetric reduction by Geotrichum candidum
 T. Matsuda, Y. Yamagishi, S. Koguchi, N. Iwai, T. Kitazume
Tetrahedron Lett. 2006, 47, 4619-4622.

25 Selective reduction of unsaturated aldehydes to unsaturated alcohols using supercritical 2-propanol
A. Daimon, T. Kamitanaka, N. Kishida, T. Matsuda, T. Harada
J. Supercritical Fluids, 2006, 37, 215-219.

24 Stereocontrolled synthesis of β-difluoromethylated materials
T. Nihei, N. Iwai, T. Matsuda, T. Kitazume
J. Org. Chem. 2005, 70, 5912-5915.

23 Rate enhancement of lipase-catalyzed reaction in supercritical carbon dioxide
T. Matsuda, K. Tsuji, T. Kamitanaka, T. Harada, K. Nakamura, T. Ikariya
Chem. Lett. 2005, 34, 1102-1103.

22 Supercritical carbon dioxide as a reaction medium for enzymatic kinetic resolution of P-chiral hydroxymethanephosphinates
M. Albrycht, P. Kielbasinski, J. Drabowicz, M. Mikolajczyk, T. Matsuda, T. Harada, K. Nakamura
Tetrahedron: Asymmetry, 2005, 16, 2015-2018.

21 A Systematic investigation of Saccharomyces cerevisiae enzymes catalyzing carbonyl reductions
I. A. Kaluzna, T. Matsuda, A. K. Sewall, M. R. Martzen, J. D. Stewart
J. Am. Chem. Soc. 2004, 126, 12827-12832.

20 High-efficiency and minimum-waste continuous kinetic resolution of racemic alcohols by using lipase in supercritical carbon dioxide
T. Matsuda, K. Watanabe, T. Harada, K. Nakamura, Y. Arita, Y. Misumi, S. Ichikawa, T. Ikariya
Chem. Commun. 2004, 2286-2287.

19 Reactions of supercritical alcohols with unsaturated hydrocarbons
T. Nakagawa, H. Ozaki, T. Kamitanaka, H. Takagi, T. Matsuda, T. Kitamura, T. Harada
J. Supercritical Fluids, 2003, 27, 255-261.

18 Control of enantioselectivity of lipase catalyzed esterification in supercritical carbon dioxide by tuning the pressure and temperature
T. Matsuda, R. Kanamaru, K. Watanabe, T. Kamitanaka, T. Harada, K. Nakamura
Tetrahedron: Asymmetry, 2003, 14, 2087-2091.

17 Crystallization Condition of Glassy Syndiotactic Polystyrene in Supercritical CO2
T. Nakaoki, Y. Fukuda, E. Nakajima, T. Matsuda, T. Harada
Polymer Journal, 2003, 35, 430-435.

16 Reduction of acetophenone using supercritical 2-propanol: the substituent effect and the deuterium kinetic isotope effect
T. Kamitanaka, T. Matsuda, T. Harada
Tetrahedron Lett. 2003, 44, 4551-4553.

15 Biocatalytic reduction of ketones by a semi-continuous flow process using supercritical carbon dioxide
T. Matsuda, K. Watanabe, T. Kamitanaka, T. Harada, K. Nakamura
Chem. Commun. 2003, 1198-1199.

14 Asymmetric reduction of simple aliphatic ketones with dried cells of Geotrichum candidum
T. Matsuda, Y. Nakajima, T. Harada, K. Nakamura
Tetrahedron: Asymmetry, 2002, 13, 971-974.

13 Control on enantioselectivity with pressure for lipase catalyzed esterification in supercritical carbon dioxide
T. Matsuda, R. Kanamaru, K. Watanabe, T. Harada, K. Nakamura
Tetrahedron Lett. 2001, 42, 8319-8321.

12 Conversion of pyrrole to pyrrole-2-carboxylate by cells of B. megaterium in supercritical CO2
T. Matsuda, Y. Ohashi, T. Harada, R. Yanagihara, T. Nagasawa, K. Nakamura
Chem. Commun. 2001, 2194-2195.

11 Asymmetric synthesis of (R)-2-chloro-1-(m-chlorophenyl)ethanol using acetone powder of Geotrichum candidum
 H. Hamada, T. Miura, H. Kumobayashi, T. Matsuda, T. Harada, K. Nakamura
Biotechnol. Lett. 2001, 23, 1603-1606.

10 Alcohol dehydrogenase is active in supercritical carbon dioxide
T. Matsuda, T. Harada, K. Nakamura
Chem. Commun. 2000, 1367-1368.

9 Mechanism for improving stereoselectivity for asymmetric reduction using acetone powder of microorganism
T. Matsuda, T. Harada, N. Nakajima, K. Nakamura
Tetrahedron Lett. 2000, 41, 4135-4138.

8 Two classes of enzymes of opposite stereochemistry in an organism: one for fluorinated and another for non-fluorinated substrates
T. Matsuda, T. Harada, N. Nakajima, T. Itoh, K. Nakamura
J. Org. Chem. 2000, 65, 157-163.

7 Stereoselective oxidation and reduction by immobilized Geotrichum candidum in an organic solvent
K. Nakamura, Y. Inoue, T. Matsuda, I. Misawa
J. Chem. Soc. Perkin Trans. 1, 1999, 2397-2402.

6 Asymmetric reduction of ketones by the acetone powder of Geotrichum candidum
K. Nakamura, T. Matsuda
J. Org. Chem. 1998, 63, 8957-8964.

5 Asymmetric reduction of trifluoromethyl ketones containing a sulfur functionality by the alcohol dehydrogenase from Geotrichum
K. Nakamura, T. Matsuda, M. Shimizu, T. Fujisawa
Tetrahedron, 1998, 54, 8393-8402.

4 Asymmetric synthesis of (S)-arylalkanols by microbial reduction
K. Nakamura, T. Matsuda, A. Ohno
Tetrahedron: Asymmetry, 1996, 7, 3021-3024.

3 Different stereochemistry for the reduction of trifluoromethyl ketones and methyl ketones catalyzed by alcohol dehydrogenase from Geotrichum
K. Nakamura, T. Matsuda, T. Itoh, A. Ohno
Tetrahedron Lett. 1996, 37, 5727-5730.

2 Asymmetric reduction of ketones by the acetone powder of Geotrichum candidum
K. Nakamura, K. Kitano, T. Matsuda, A. Ohno
Tetrahedron Lett. 1996, 37, 1629-1632.

1 Microbial deracemization of 1-arylethanol
K. Nakamura, Y. Inoue, T. Matsuda, A. Ohno
Tetrahedron Lett. 1995, 36, 6263-6266.


Reviews etc.

83 酵素を触媒としてCO2を有効利用する有機合成 Enzymatic organic synthesis effectively utilizing CO2 奥悠莉、松田知子 エネルギー・資源, 2025, 46, 219-223. 82 好熱菌由来リンゴ酸酵素による二酸化炭素固定
奥 悠莉、松田 知子
B&I, 2025, 83(1), 28-29.
ISSN 0914-8981

81 Medium engineering of lipase-catalyzed reaction using CO2
T. Matsuda, H. N. Hoang, J. Am. Oil Chem. Soc. 2025, 102, 401-412.
10.1002/aocs.12895

80 Chapter 6 - Laccases: biological functions and potential applications
L. H. L. Viet, T. Matsuda, I. K. H. Leung
In Laccase and Polyphenol Oxidase; Biochemistry and Biotechnological Applications 1st Edition
Ed. I. K. H. Leung, Elsevier, 2025, p133-152.
Paperback ISBN: 9780443133015
eBook ISBN: 9780443133008

79 Chapter 4 Control of the activity and enantioselectivity in biocatalyzed procedures: immobilization, medium engineering and protein engineering
Z. Tang, F. I. Alghiffary, T. Matsuda
In Biocatalysis in Asymmetric Synthesis 1st Edition Eds: G. D. Gonzalo, A. R. Alcántara, Elsevier, 2024, p101-131.
10.1016/B978-0-443-19057-5.00006-6

78 Application of immobilized enzymes in flow biocatalysis for efficient synthesis
Z. Tang, Y. Oku, T. Matsuda, Org. Process Res. Dev. 2024, 28, 1308-1326.
10.1021/acs.oprd.3c00405

77 Recent advances in enzyme immobilization utilizing nanotechnology for biocatalysis
K. T.sriwong, T. Matsuda
Org. Process Res. Dev. 2022, 26, 1857-1877.
10.1021/acs.oprd.1c00404

76 Chapter 9 Application of Nonaqueous Media in Biocatalysis
A. A. Koesoema, T. Matsuda
In Biocatalysis for Practitioners: Techniques, Reactions and Applications, Eds. G. d. Gonzalo, I. Lavandera, Wiley-VCH GmbH, 2021, p 247-274.

75 12.10.7 酵素反応
松田知子
化学便覧 基礎編 改訂6版 公益社団法人 日本化学会 (編集), 丸善, 2021.

74 Impact and relevance of alcohol dehydrogenase enantioselectivities on biotechnological applications
A. A. Koesoema, D. M. Standley, T. Senda, T. Matsuda
Appl. Microbiol. Biotechnol. 2020, 104, 2897－2909.

73 CO2膨張液体を利用した酵素反応による有機化学合成
Hai Nam Hoang, 山田眞二郎, 松田知子
分離技術, 2019, 49(2), 9-12.

72 Chapter 7. Biocatalysis in Supercritical and Liquid Carbon Dioxide and Carbon Dioxide-expanded Liquids
H. N. Hoang, K. R. A. Are, T. Matsuda
In Supercritical and Other High-pressure Solvent Systems: For Extraction, Reaction and Material Processing (Green Chemistry Series) Eds. A. J. Hunt, T. M Attard, Royal Society of Chemistry, 2018, p 191 － 220.

71 Chapter 1. Biotransformation Using Liquid and Supercritical CO2
H. N. Hoang, T. Matsuda
In Future directions in biocatalysis, 2nd edition, Ed. T. Matsuda, Elsevier, 2017, p 3-25.

70 Future directions in biocatalysis, 2nd edition
T. Matsuda, Ed. Elsevier, Amsterdam, 2017.

69 超臨界流体および液体二酸化炭素を用いる酵素による物質変換 松田知子
Hai Nam Hoang
Biocatalysis in supercritical or liquid carbon dioxide Tomoko Matsuda, Hai Nam Hoang
冷凍, 2017, 92 (1072), 32-35.

68 Chapter 11. Enzymatic Asymmetric Reduction of Carbonyl Compounds
T. Matsuda, R. Yamanaka, K. Nakamura In Green Biocatalysis, Ed. R. N. Patel, Wiley & Sons, 2016, p 307-330.ISBN: 978-1-118-82229-6

67 Chapter 3. Biocatalysis in organic solvents, supercritical fluids and ionic liquids
C. Cao, T. Matsuda In Organic synthesis using biocatalysis, Eds. A. Goswami, J. D. Stewart, Elsevier, 2016, p 67-99. ISBN: 978-0-12-411518-7

66 Geotrichum candidum由来の高立体選択的アルコール脱水素酵素の構造解析
Structural analysis of Geotrichum candidum alcohol dehydrogenase with excellent enantioselectivity
杉山陽祐,千田美紀,千田俊哉, 松田知子 Photon Factory Activity Report, 2014, Volume 2013 B, #31.

65 二酸化炭素を有効利用する酵素反応の制御
松田知子
化学工学, 2014, 78, 471-472.

64 Biocatalytic asymmetric reduction of C=O and activated C=C bonds in stereoselective synthesis
T. Matsuda, R. Yamanaka, K. Nakamura In Stereoselective synthesis of drugs and natural products, Eds. V. Andrushko, N. Andrushko, Wiley, 2013, p. 1015-1042. ISBN: 978-1-118-03217-6

63 第２章 第7節 超臨界流体の触媒反応場としての応用
松田知子 触媒の設計●反応制御 事例集, (株)技術情報協会, 2013, p.106-111.

62 12節 超臨界二酸化炭素を溶媒に用いた酵素反応
松田知子 新しい溶媒を用いた有機合成, S&T出版株式会社, 2013, p.109-119.

61 Recent progress in biocatalysis using supercritical carbon dioxide
T. Matsuda J. Biosci. Bioeng. 2013, 115, 233-241. DOI: 10.1016/j.jbiosc.2012.10.002

60 超臨界二酸化炭素中での微生物酵素による合成反応の開発
松田知子 科研費NEWS, 文部科学省 日本学術振興会, 2011-12, 4, 11-11.

59 Asymmetric catalytic synthesis in supercritical fluids
T. Matsuda In Catalytic methods in asymmetric synthesis: advanced materials, techniques, and applications, Eds. M. Gruttadauria, F. Giacalone, New Jersey, Wiley, 2011, Chapter 9, p. 373－390.(http://onlinelibrary.wiley.com/book/10.1002/9781118087992)

58 5章 酸化還元反応 －酵素化学への展開
松田知子 生命理工系のための大学院基礎講座 －有機化学（湯浅英哉 編）東京工業大学出版会, 2011, p. 91-109.

57 Chiral pyrrolidine-substituted ionic liquid-mediated activation of enzyme
T. Itoh, Y. Abe, T. Hirakawa, N. Okano, S. Nakajima, S. Hayase, M. Kawatsura, T. Matsuda, K. Nakamura In Ionic liquid applications: pharmaceuticals, therapeutics, and biotechnology, Ed. S. Malhotra, ACS Symposium Series, American Chemical Society: Washington, DC, 2010, Chapter 13, p. 155-167.

56 超臨界二酸化炭素と酵素を利用する有用化合物の合成
松田知子 生物工学, 2010, 88, 516-519. 55 超臨界CO2中での酵素を用いる有機合成反応の開発 松田知子 未来材料, 2010, 10, 27-32.

54 4編4章1節2. 超臨界流体
松田知子 酵素利用技術体系（小宮山眞 監修）エヌ・ティー・エス, 2010, p. 328-332.

53 酵素による光学活性化合物の合成
松田知子 医療・診断をめざす先端バイオテクノロジー（関根光雄 編）工学図書, 2009, p. 131-140.

52 超臨界二酸化炭素中での生体触媒反応を利用したグリーンケミストリー
Green Biocatalysis in Supercritical Carbon Dioxide 松田知子 GSCN News Letter, グリーン・サスティナブルケミストリー ネットワーク, 33, 2009.

51 化学工学年鑑2009 9章 超臨界流体 9.4章 反応・物質変換
松田知子 化学工業, 2009, 73, 516-517.

50 酵素反応
松田知子、阿部泰祐、福井秀介 化学工学会 超臨界部会 活動成果集(ワーキンググループ活動報告書No.6)2009, 139-143.

49 [和訳] 超臨界流体
松田知子 カーク・オスマー 化学技術・環境ハンドブック グリーン・サステイナブルケミストリー, 丸善, 2009, 11章, p. I-273-289.

48 超臨界流体中で機能する酵素
松田知子
化学工学, 2009, 73, 344-346.

47 Recent progress in biocatalysis for asymmetric oxidation and reduction
T. Matsuda, R. Yamanaka, K. Nakamura
Tetrahedron: Asymmetry, 2009, 20, 513-557.

46 実用化を目指す超臨界二酸化炭素中の生体触媒反応
Practical Biocatalysis in Supercritical Carbon Dioxide
松田知子
月刊バイオインダストリー, シーエムシー出版, 2009, 26, 54-59.

45 超臨二酸化炭素を利用する酵素反応
松田知子
日本化学会 生体機能関連化学部会 ニュースレター, 2009, 23(4), 2-5.

44 超臨界二酸化炭素中における酵素反応
松田知子
超臨界流体入門（化学工学会超臨界流体部会 編）丸善, 2008, p. 135-142.

43 超臨界二酸化炭素を利用した生体触媒反応の開発
松田知子、北爪智哉、原田忠夫、中村薫
超臨界流体技術の開発と応用 (佐古 猛 監修) シーエムシー出版, 2008, p178-185.

42 触媒は酵素! 超臨界CO2での有機合成 - CO2を有効利用するバイオプロセスの開発
松田知子
化学, 2008, 63, 40-41.

41 Enzyme-catalyzed reduction of carbonyl compounds
K. Nakamura, T. Matsuda
In Modern reduction methods, Eds. P. G. Andersson, I. J. Munslow, Wiley-VCH, Weinheim, 2008, 209-234.

40 II-5章 ベンゼン II-7章 カルボン酸 II-14.8-11章 総合演習問題
北爪智哉、松田知子
バイオ系のための基礎化学問題集
(三原久和、梶原将、湯浅英哉、小畠英理 編) 講談社サイエンティフィク, 2008, p. 107-110, 117-120, 156-157.

39 Enzymatic reduction reaction
K. Nakamura, T. Matsuda
In Asymmetric organic synthesis with enzymes, Eds. V.
Gotor, I. Alfonso, E. Carcia-Urdiales, Wiley-VCH, Weinheim, 2008, 193-228.

38 超臨界流体中における酵素反応
松田知子
化学工学会 超臨界部会 活動成果集(ワーキンググループ活動報告書No.5)2007, 171-175.

37 超臨界二酸化炭素中における酵素反応の新展開
Recent progress on enzymatic reactions in supercritical carbon dioxide
松田知子
Jasco Report 超臨界最新技術 特集第9号, 2007, 17-20.

36 Future directions in biocatalysis
T. Matsuda, Ed. Elsevier, Amsterdam, 2007.

35 私が研究者になるまで 愛情に囲まれて
松田知子
学術の動向, 2007, 12(6), 82-83.

34 超臨界CO2と酵素による有用物質の合成
松田知子
バイオプロセスハンドブック, エヌ・ティー・エス, 2007, p. 172-178.

33 Biocatalysis in Water
K. Nakamura, T. Matsuda
in Organic Reactions in Water - Principles, Strategies and Applications, Ed. U. M. Lindstr嗄, Blackwell Publishing Ltd., Oxford, 2007, p301-349.

32 超臨界流体を用いる環境調和型有機合成反応
松田知子
化学と工業, 2007, 60, 226-227.

31 酵素を用いるフッ素化合物の合成
松田知子, 岩井伯隆, 北爪智哉
触媒, 2007, 49, 31-36.

30 超臨界二酸化炭素を利用した生体触媒反応の開発
松田知子、北爪智哉、原田忠夫、中村薫
月刊バイオインダストリー, シーエムシー出版, 2007, 24, 24-31.

29 二酸化炭素の中での酵素を利用する有用物質の生産法の開発
松田知子
大学婦人協会会報, 2006, 222, 6-6.

28 Biocatalytic Reduction of Carbonyl Groups
K. Nakamura, T. Matsuda
Current Organic Chem., 2006, 10, 1217-1246.

27 超臨界CO2と酵素で有用物質を合成
松田知子
日刊工業新聞, 2006年4月5日p25(科学技術コラム欄)

26 Synthesis of Chiral Fluorinated Materials via Biotransformation
T. Kitazume, T. Matsuda, K. Nakamura
In Advances in Organic Synthesis, Vol. 2, Eds. K. Laali, A. Rahman (Ed.), Bentham Science Publishers. The Netherlands, 2006, 463-490.

25 超臨界CO2中での酵素反応による有用物質の合成
松田知子
The Chemical Times, 2005, 197, 8-13. (関東化学株式会社Kanto Chemical Co., Inc.)

24 超臨界二酸化炭素を利用するグリーンバイオプロセスの開発
松田知子
ケミカルエンジニアリング, 2005, 50, 636-642.

23 Asymmetric synthesis using hydrolytic enzymes in supercritical carbon dioxide
T. Matsuda, T. Harada, K. Nakamura, T. Ikariya
Tetrahedron: Asymmetry, 2005, 16, 909-915.

22 Biocatalysis in supercritical CO2
T. Matsuda, T. Harada, K. Nakamura
Current Organic Chem., 2005, 9, 299-315.

21 Enzymatic kinetic resolution
K. Nakamura, T. Matsuda
in Enantimer Separation: Fundamentals and Practical Methods, Ed. F. Toda, Kluwer Academic Publishers, Dordrecht, 2004, p231-266.

20 超臨界二酸化炭素中の酵素反応
松田知子
化学工学会 超臨界部会 活動成果集(ワーキンググループ活動報告書No.4)2004, 160-164.

19 Carboxylation of pyrrole to pyrrole-2-carboxylate by cells of Bacillus megaterium in supercritical carbon dioxide
T. Matsuda, T. Harada, T. Nagasawa, K. Nakamura,
in Catalysts for Fine Chemical Synthesis, Vol. 3, Metal Catalysed Carbon-Carbon Bond-Forming Reactions, Edited by S. M. Roberts, J. Xiao, J. Whittall, and T. Pickett, John Wiley & Sons, West Sussex, 2004, p. 247 - 250.

18 生体触媒ゴードン国際会議（学術集会報告（国際））
松田知子
酵素工学ニュース, 2004, 52, 58-59.

17 超臨界二酸化炭素中の酵素反応による有用物質の新規効率的合成
松田知子, 原田忠夫, 中村薫, 碇屋隆雄
Jasco Report 超臨界最新技術 特集第8号, 2004, 10-15

16 Enzymatic reactions in supercritical CO2: carboxylation, asymmetric reduction and esterification
T. Matsuda, K. Watanabe, T. Harada, K. Nakamura
Catalysis Today, 2004, 96, 103-111.

15 Organic synthesis using enzymes in supercritical carbon dioxide
T. Matsuda, T. Harada, K. Nakamura
Green Chem., 2004, 6, 440-444.

14 超臨界二酸化炭素中における環境調和型バイオ触媒反応
松田知子, 原田忠夫, 中村薫, 碇屋隆雄
ケミカルエンジニアリング, 2004, 49, 711-716.

13 9-2 微生物と酵素を利用する酸化反応
中村薫, 松田知子
実験化学講座 改訂第５版 17巻(日本化学会 編)丸善, 2004, p. 404-417.

12 12.10.6 酵素反応
中村薫, 松田知子
化学便覧 基礎編II 改訂第５版 (日本化学会 編) 丸善, 2004, p. II-539 - II-547.

11 Recent developments in asymmetric reduction of ketones with biocatalysts
K. Nakamura, R. Yamanaka, T. Matsuda, T. Harada
Tetrahedron: Asymmetry, 2003, 14, 2659-2681.

10 不斉還元における生体触媒法と化学法の違い
中村薫, 山中理央, 松田知子
化学工業, 2003, 54, 89-92.

9 超臨界二酸化炭素中の酵素反応
松田知子, 原田忠夫
超臨界流体(3) 分離を中心とする超臨界流体の研究や利用技術の現状（長浜邦雄 編）
分離技術, 2002, 32, 302-302.

8 超臨界二酸化炭素を利用した生体触媒反応の開発 -リパーゼ、アルコール脱水素酵素、脱炭酸酵素の反応
松田知子, 原田忠夫, 中村薫
Jasco Report 超臨界最新技術 特集第6号, 2002, 55-58.

7 Chiral synthesis of secondary alcohols using Geotrichum candidum
K. Nakamura, T. Matsuda, T. Harada
Chirality, 2002, 14, 703-708.

6 超臨界二酸化炭素中におけるバイオプロセス
松田知子, 原田忠夫, 中村薫
ファインケミカル, 2002, 31, 40-49.

5 生体触媒による有用物質変換と環境浄化
中村薫, 山中理央, 松田知子
化学, 2002, 57, 32-36.

4 生体触媒による有用物質変換のメリット・デメリット
中村薫, 山中理央, 松田知子
化学工業, 2002, 53, 437-442.

3 Reduction reactions in Enzyme Catalysis in Organic Synthesis A Comprehensive Handbook
K. Nakamura, T. Matsuda
Eds. K. Drauz, H. Waldmann, Wiley-VCH Verlag GmbH, Weinheim, 2002, p. 991-1047.

2 入手容易な生体触媒を利用する不斉合成
中村薫, 松田知子
グリーンバイオテクノロジー 持続的社会のための生物工学
（海野肇, 岡畑恵雄 編）講談社, 2002, p. 19-32.

1 Enantioselective oxidation and reduction by Geotrichum candidum
T. Matsuda, T. Harada, K. Nakamura
J. Synthetic Organic Chem. Japan, 2001, 59, 659-669.
チチカビによる立体選択的酸化還元反応
松田知子, 原田忠夫, 中村薫
有機合成協会誌, 2001, 59, 659-669.


東京科学大学
生命理工学院
生命理工学系
松田研究室

〒226-8501 神奈川県横浜市緑区長津田町4259 J3-5
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電話 045-924-5757
メール tmatsuda[at]bio.titech.ac.jp

Institute of Science Tokyo
School of Life Science and Technology
Department of Life Science and Technology
Matsuda Research Group

J3-5 4259 Nagatsuta-cho, Midori-ku, Yokohama-shi, Kanagawa-ken, Japan 226-8501
Office room 913, Student Room 914, Experiment rooms 915 and 921
Tel. 045-924-5757
Email tmatsuda[at]bio.titech.ac.jp