T. Hoshino

发表

Biochemical characterization of the water‐soluble squalene synthase from Methylococcus capsulatus and the functional analyses of its two DXXD(E)D motifs and the highly conserved aromatic amino acid residues

S. Sasaki, Kana Ohtake, Naoki Saito, 2014, The FEBS journal.

Violacein and related tryptophan metabolites produced by Chromobacterium violaceum: biosynthetic mechanism and pathway for construction of violacein core

T. Hoshino, 2011, Applied Microbiology and Biotechnology.

Functional analysis of the DXDDTA motif in squalene-hopene cyclase by site-directed mutagenesis experiments: initiation site of the polycyclization reaction and stabilization site of the carbocation intermediate of the initially cyclized A-ring.

T. Hoshino, T. Sato, Tsutomu Sato, 1999, Bioscience, biotechnology, and biochemistry.

Novel tryptophan metabolites, chromoazepinone A, B and C, produced by a blocked mutant of Chromobacterium violaceum, the biosynthetic implications and the biological activity of chromoazepinone A and B.

M. Ishibashi, T. Hoshino, Kazufumi Toume, 2010, Organic & biomolecular chemistry.

Biosynthesis of violacein: a genuine intermediate, protoviolaceinic acid, produced by VioABDE, and insight into VioC function.

T. Hoshino, N. Nikaidou, Takeshi Watanabe, 2007, Chemical communications.

Biosynthesis of Violacein: Origins of Hydrogen, Nitrogen and Oxygen Atoms in the 2-Pyrrolidone Nucleus

T. Hoshino, T. Takano, S. Hori, 1987 .

Biosynthesis of Violacein: a Novel Rearrangement in Tryptophan Metabolism with a 1,2-Shift of the Indole Ring

T. Hoshino, T. Uchiyama, T. Kondo, 1987 .

Biosynthesis of Violacein: Evidence for the Intermediacy of 5-Hydroxy-L-tryptophan and the Structure of a New Pigment, Oxyviolacein, Produced by the Metabolism of 5-Hydroxytryptophan

T. Hoshino, N. Ogasawara, 1990 .

Studies on the Biosynthesis of Violacein, Part IV. A New Metabolite of Tryptophan, Chromopyrrolic Acid, Produced by Chromobacterium violaceum.

Y. Kojima, T. Hoshino, T. Uchiyama, 1993 .

Biosynthesis of violacein: oxygenation at the 2-position of the indole ring and structures of proviolacein, prodeoxyviolacein and pseudoviolacein, the plausible biosynthetic intermediates of violacein and deoxyviolacein

T. Hoshino, Toru Hayashi, T. Odajima, 1995 .

Studies on the biosynthesis of violacein. Part 9.1 Green pigments possessing tetraindole and dipyrromethene moieties, chromoviridans and deoxychromoviridans, produced by a cell-free extract of Chromobacterium violaceum and their biosynthetic origins

T. Hoshino, A. Momen, Takaaki Mizuoka, 1998 .

Biosynthesis of Violacein: Intact Incorporation of the Tryptophan Molecule on the Oxindole Side, with Intramolecular Rearrangement of the Indole Ring on the 5-Hydroxyindole Side

T. Hoshino, A. Momen, 2000, Bioscience, biotechnology, and biochemistry.

Substrate specificity of Rv3378c, an enzyme from Mycobacterium tuberculosis, and the inhibitory activity of the bicyclic diterpenoids against macrophage phagocytosis.

Chiaki Nakano, T. Hoshino, Takahiro Ootsuka, 2011, Organic & biomolecular chemistry.

O-acetylated xyloglucan in extracellular polysaccharides from cell-suspension cultures of Mentha.

T. Suzuki, T. Hoshino, T. Uchiyama, 1996, Phytochemistry.

Strictly Conserved Residues in Euphorbia tirucalli β‐Amyrin Cyclase: Trp612 Stabilizes Transient Cation through Cation–π Interaction and CH–π Interaction of Tyr736 with Leu734 Confers Robust Local Protein Architecture

Chiaki Nakano, T. Hoshino, Takumi Watanabe, 2018, Chembiochem : a European journal of chemical biology.

Euphorbia tirucalli β‐Amyrin Synthase: Critical Roles of Steric Sizes at Val483 and Met729 and the CH–π Interaction between Val483 and Trp534 for Catalytic Action

T. Hoshino, Kazuya Nakagawa, Daichi Itoh, 2017, Chembiochem : a European journal of chemical biology.

Identification of Diterpene Biosynthetic Gene Clusters and Functional Analysis of Labdane-Related Diterpene Cyclases in Phomopsis amygdali

T. Toyomasu, W. Mitsuhashi, T. Dairi, 2008, Bioscience, biotechnology, and biochemistry.

Identification of a New Diterpene Biosynthetic Gene Cluster that Produces O‐Methylkolavelool in Herpetosiphon aurantiacus

Chiaki Nakano, T. Hoshino, Misaki Oshima, 2015, Chembiochem : a European journal of chemical biology.

Self-association of flavylium cations of anthocyanidin 3,5-diglucosides studied by circular dichroism and 1H NMR☆

T. Hoshino, 1992 .

An approximate estimate of self-association constants and the self-stacking conformation of malvin quinonoidal bases studied by 1H NMR

T. Hoshino, 1991 .

Effects of pH and concentration on the self-association of malvin quinonoidal base — electronic and circular dichroic studies

T. Hoshino, T. Goto, 1990 .

Evidence for the self-association of anthocyanins IV. PMR spectroscopic evidence for the vertical stacking of anthocyanin molecules

N. Harada, T. Hoshino, T. Goto, 1982 .

Chiral exciton coupled stacking of anthocyanins: interpretation of the origin of anomalous CD induced by anthocyanin association

N. Harada, T. Hoshino, T. Goto, 1981 .

Evidences of the self-association of anthocyanins I. Circular Dichroism of cyanin anhydrobase

T. Hoshino, T. Goto, Ushino Matsumoto, 1980 .

Structure and Inhibition of Tuberculosinol Synthase and Decaprenyl Diphosphate Synthase from Mycobacterium tuberculosis

E. Oldfield, A. H. Wang, T. Ko, 2014, Journal of the American Chemical Society.

Characterization of the Rv3378c Gene Product, a New Diterpene Synthase for Producing Tuberculosinol and (13R, S)-Isotuberculosinol (Nosyberkol), from the Mycobacterium tuberculosis H37Rv Genome

Chiaki Nakano, T. Hoshino, T. Mitsui, 2011, Bioscience, biotechnology, and biochemistry.

Mycobacterium tuberculosis H37Rv3377c encodes the diterpene cyclase for producing the halimane skeleton.

T. Dairi, Chiaki Nakano, T. Hoshino, 2005, Chemical communications.

Chemistry of Metalloanthocyanins a

N. Harada, H. Tamura, T. Hoshino, 1986 .

Convenient Preparation and Quantification of 5,5'-Diferulic Acid.

T. Hoshino, T. Uchiyama, Hirotaka Yamamoto, 1999, Bioscience, biotechnology, and biochemistry.

Biodegradation of organophosphorus insecticides by bacteria isolated from turf green soil

K. Ohshiro, T. Hoshino, T. Uchiyama, 1996 .

Characterization of isofenphos hydrolases from Arthrobacter sp. strain B-5

K. Ohshiro, T. Hoshino, T. Uchiyama, 1997 .

Novel Compounds of Octahydroheptaprenyl Mycolic Acyl Ester and Monocyclic C35-Terpene, Heptaprenylcycline B, from Non-Pathogenic Mycobacterium Species

T. Hoshino, Tsutomu Sato, R. Takagi, 2010, Bioscience, biotechnology, and biochemistry.

Biosynthesis of a novel cyclic C35-terpene via the cyclisation of a Z-type C35-polyprenyl diphosphate obtained from a nonpathogenic Mycobacterium species.

T. Hoshino, Tsutomu Sato, T. Adachi, 2008, Organic & biomolecular chemistry.

β-Amyrin Biosynthesis: The Methyl-30 Group of (3S)-2,3-Oxidosqualene Is More Critical to Its Correct Folding To Generate the Pentacyclic Scaffold than the Methyl-24 Group.

T. Hoshino, Masaki Hanaoka, Kazunari Takahashi, 2015, Chemistry.

β-Amyrin biosynthesis: catalytic mechanism and substrate recognition.

T. Hoshino, 2017, Organic & biomolecular chemistry.

β‐Amyrin Biosynthesis: Effect of Steric Bulk at the 6‐, 10‐ and 15‐Positions in the 2,3‐Oxidosqualene Backbone on Polycyclisation Cascades

T. Hoshino, Y. Sasaki, Y. Yamaguchi, 2017 .

β-Amyrin biosynthesis: the critical role of steric volume at C-19 of 2,3-oxidosqualene for its correct folding to generate the pentacyclic scaffold.

T. Hoshino, Y. Yamaguchi, Kazunari Takahashi, 2014, Organic letters.

The stabilizing effect of the acyl group on the co-pigmentation of acylated anthocyanins with C-glucosylflavones

T. Hoshino, T. Goto, U. Matsumoto, 1980 .

Circular dichroic measurements on anthocyanins in intact flower petals

T. Hoshino, 1986 .

Self-association of some anthocyanins in neutral aqueous solution

T. Hoshino, T. Goto, Ushino Matsumoto, 1981 .

Surface mannan from Glomerella cingulata.

T. Hoshino, Reiko Watanabe, N. Ogasawara, 1986 .

Squalene-hopene cyclase: catalytic mechanism and substrate recognition.

T. Hoshino, Tsutomu Sato, 2002, Chemical communications.

Synthesis of Isotopically Labelled Oligoprenyl Diphosphates and Their Application in Mechanistic Investigations of Terpene Cyclases

Jeroen S. Dickschat, Chiaki Nakano, T. Hoshino, 2014 .

Structure, function and inhibition of ent-kaurene synthase from Bradyrhizobium japonicum

E. Oldfield, S. Hsu, T. Ko, 2014, Scientific Reports.

Characterization of the Rv3377c Gene Product, a Type‐B Diterpene Cyclase, from the Mycobacterium tuberculosis H37 Genome

Chiaki Nakano, T. Hoshino, 2009, Chembiochem : a European journal of chemical biology.

A proposed structure of commelinin, a sky-blue anthocyanin complex obtained from the flower petals of

T. Hoshino, T. Goto, S. Takase, 1979 .

A novel sphingophosphonolipid head group 1-hydroxy-2-aminoethyl phosphonate in Bdellovibrio stolpii

T. Hoshino, E. Kaneshiro, Masaharu Nakajima, 2001, Lipids.

β-Amyrin synthase from Euphorbia tirucalli. Steric bulk, not the π-electrons of Phe, at position 474 has a key role in affording the correct folding of the substrate to complete the normal polycyclization cascade.

Chiaki Nakano, T. Hoshino, Chika Nakada, 2014, Organic & biomolecular chemistry.

Enzymatic cyclization reactions of geraniol, farnesol and geranylgeraniol, and those of truncated squalene analogs having C20 and C25 by recombinant squalene cyclase.

T. Hoshino, S. Nakano, Yuko Kumai, 2004, Organic & biomolecular chemistry.

Sesquarterpenes (C35 terpenes) biosynthesized via the cyclization of a linear C35 isoprenoid by a tetraprenyl-β-curcumene synthase and a tetraprenyl-β-curcumene cyclase: identification of a new terpene cyclase.

T. Hoshino, Tsutomu Sato, H. Hoshino, 2011, Journal of the American Chemical Society.

Identification of Novel Sesterterpene/Triterpene Synthase from Bacillus clausii

Y. Murata, T. Shinada, Chiaki Nakano, 2013, ChemBioChem.

Insight into the pathway for biosynthesis of sesquarterpenes in nonpathogenic Mycobacterium species: identification of heptaprenylcycli-14E,18E-diene

Chiaki Nakano, T. Hoshino, Tsutomu Sato, 2012 .

Insight into C35 terpene Biosyntheses by Nonpathogenic Mycobacterium Species: Functional Analyses of Three Z‐Prenyltransferases and Identification of Dehydroheptaprenylcyclines

T. Hoshino, Tsutomu Sato, Y. Orito, 2010, Chembiochem : a European journal of chemical biology.

Functional analysis of phenylalanine 365 in hopene synthase, a conserved amino acid in the families of squalene and oxidosqualene cyclases†

T. Hoshino, Tsutomu Sato, 1999 .

Chemo-enzymatic syntheses of drimane-type sesquiterpenes and the fundamental core of hongoquercin meroterpenoid by recombinant squalene-hopene cyclase.

T. Hoshino, Y. Yonemura, Takuro Ohyama, 2012, Organic & biomolecular chemistry.

Cyclization of squalene from both termini: identification of an onoceroid synthase and enzymatic synthesis of ambrein.

T. Hoshino, Tsutomu Sato, Daijiro Ueda, 2013, Journal of the American Chemical Society.

Bifunctional triterpene/sesquarterpene cyclase: tetraprenyl-β-curcumene cyclase is also squalene cyclase in Bacillus megaterium.

T. Hoshino, Tsutomu Sato, H. Hoshino, 2011, Journal of the American Chemical Society.

Triterpene cyclases from Oryza sativa L.: cycloartenol, parkeol and achilleol B synthases.

Chiaki Nakano, T. Hoshino, Tsutomu Sato, 2011, Organic letters.

Sterol Biosynthesis by a Prokaryote: First in Vitro Identification of the Genes Encoding Squalene Epoxidase and Lanosterol Synthase from Methylococcus capsulatus

Chiaki Nakano, T. Hoshino, M. Onodera, 2007, Bioscience, biotechnology, and biochemistry.

Cyclization cascade of the C33-bisnorheptaprenoid catalyzed by recombinant squalene cyclase.

T. Hoshino, Jun Cheng, 2009, Organic & biomolecular chemistry.

Production of epoxydammaranes by the enzymatic reactions of (3R)- and (3S)-2,3-squalene diols and those of 2,3:22,23-dioxidosqualenes with recombinant squalene cyclase and the mechanistic insight into the polycyclization reactions.

T. Hoshino, Y. Yonemura, T. Abe, 2007, Organic & biomolecular chemistry.

Enzymatic cyclizations of squalene analogs with threo- and erythro-diols at the 6,7- or 10,11-positions by recombinant squalene cyclase. Trapping of carbocation intermediates and mechanistic insights into the product and substrate specificities.

T. Hoshino, T. Abe, 2005, Organic & biomolecular chemistry.

Chemical structure of cichorinotoxin, a cyclic lipodepsipeptide that is produced by Pseudomonas cichorii and causes varnish spots on lettuce

T. Hoshino, T. Uchiyama, T. Shirakawa, 2019, Beilstein journal of organic chemistry.

Acaricide-Mediated Suppression of Panonychus Citri (Mcgregor) (Acari: Tetranychidae) in Pear Orchards in Japan

T. Gotoh, T. Hoshino, T. Korenaga, 2008 .

13C and 139La NMR Studies of La2@C80: First Evidence for Circular Motion of Metal Atoms in Endohedral Dimetallofullerenes

Hideyuki Funasaka, Takeshi Akasaka, Markus Wälchli, 1997 .

Oryza sativa Parkeol Cyclase: Changes in the Substrate‐Folding Conformation and the Deprotonation Sites on Mutation at Tyr257: Importance of the Hydroxy Group and Steric Bulk

T. Hoshino, Asuka Suzuki, Ryousuke Ito, 2019, Chembiochem : a European journal of chemical biology.

Deletion of the Gly600 residue of Alicyclobacillus acidocaldarius squalene cyclase alters the substrate specificity into that of the eukaryotic-type cyclase specific to (3S)-2,3-oxidosqualene.

T. Hoshino, Tsutomu Sato, K. Shimizu, 2004, Angewandte Chemie.

Squalene-hopene cyclase: final deprotonation reaction, conformational analysis for the cyclization of (3R,S)-2,3-oxidosqualene and further evidence for the requirement of an isopropylidene moiety both for initiation of the polycyclization cascade and for the formation of the 5-membered E-ring.

T. Kondo, T. Hoshino, Tsutomu Sato, 2004, Organic & biomolecular chemistry.

Purification, kinetics, inhibitors and CD for recombinant β‐amyrin synthase from Euphorbia tirucalli L and functional analysis of the DCTA motif, which is highly conserved among oxidosqualene cyclases

T. Hoshino, Yukari Masukawa, Ryousuke Ito, 2013, The FEBS journal.

Squalene-hopene cyclase: insight into the role of the methyl group on the squalene backbone upon the polycyclization cascade. Enzymatic cyclization products of squalene analogs lacking a 26-methyl group and possessing a methyl group at C7 or C11.

T. Hoshino, S. Nakano, S. Ohashi, 2004, Organic and biomolecular chemistry.

Mutated variants of squalene-hopene cyclase: enzymatic syntheses of triterpenes bearing oxygen-bridged monocycles and a new 6,6,6,6,6-fusded pentacyclic scaffold, named neogammacerane, from 2,3-oxidosqualene.

T. Hoshino, Takashi Watanabe, Y. Fukuda, 2018, Organic & biomolecular chemistry.

Alicyclobacillus acidocaldarius Squalene‐Hopene Cyclase: The Critical Role of Steric Bulk at Ala306 and the First Enzymatic Synthesis of Epoxydammarane from 2,3‐Oxidosqualene

T. Hoshino, Tsutomu Sato, Takashi Watanabe, 2018, Chembiochem : a European journal of chemical biology.

Squalene-Hopene Cyclase: Mechanistic Insights into the Polycyclization Cascades of Squalene Analogs Bearing Ethyl and Hydroxymethyl Groups at the C-2 and C-23 Positions.

T. Hoshino, Yuri Terasawa, Ikki Kaneko, 2018, Chemistry.

Squalene‐Hopene Cyclase: On the Polycyclization Reactions of Squalene Analogues Bearing Ethyl Groups at Positions C‐6, C‐10, C‐15, and C‐19

T. Hoshino, Y. Sasaki, Kazunari Takahashi, 2018 .

Further Insight into Polycyclization Cascades of Acyclic Geranylfarnesol and its Acetate by Squalene-hopene Cyclase from Alicyclobacillus Acidocaldarius

Chiaki Nakano, T. Hoshino, G. Shi, 2016, Natural product communications.

Reviewing the polyolefin cyclization reaction of the c(35) polyprene catalyzed by squalene-hopene cyclase.

T. Hoshino, Tsutomu Sato, Yuko Kumai, 2009, Chemistry.

Site-directed Mutagenesis Experiments on the Putative Deprotonation Site of Squalene-hopene Cyclase from Alicyclobacillus acidocaldarius

T. Hoshino, Tsutomu Sato, M. Kouda, 2004, Bioscience, biotechnology, and biochemistry.

Importance of the methyl group at C10 of squalene for hopene biosynthesis and novel carbocyclic skeletons with 6/5 + 5/5 + (6) ring system(s).

T. Hoshino, S. Ohashi, 2002, Organic letters.

Unnatural natural triterpenes produced by altering isoleucine into alanine at position 261 in hopene synthase and the importance of having the appropriate bulk size at this position for directing the stereochemical destiny during the polycyclization cascade

T. Hoshino, 2000 .

Functional analysis of Phe605, a conserved aromatic amino acid in squalene–hopene cyclases

T. Hoshino, Tsutomu Sato, T. Abe, 2000 .

New cyclization mechanism for squalene: a ring-expansion step for the five-membered C-ring intermediate in hopene biosynthesis.

T. Hoshino, T. Abe, S. Ohashi, 1999, Bioscience, biotechnology, and biochemistry.

The cyclization mechanism of squalene in hopene biosynthesis: the terminal methyl groups are critical to the correct folding of this substrate both for the formation of the five-membered E-ring and for the initiation of the polycyclization reaction†

T. Hoshino, 1999 .

Overexpression of squalene-hopene cyclase by the pET vector in Escherichia coli and first identification of tryptophan and aspartic acid residues inside the QW motif as active sites.

T. Hoshino, T. Sato, Y. Kanai, 1998, Bioscience, biotechnology, and biochemistry.

On the cyclization mechanism of squalene: a ring expansion process of the five-membered D-ring intermediate

T. Hoshino, Tsutomu Sato, T. Abe, 1998 .

Synthesis of 10,15‐[13C2]‐squalene and ‐DL‐squalene oxide

H. Williams, T. Hoshino, A. Scott, 1990 .

Isolation and structure of a new organic acid accumulated in tulip plant (Tulipa gesneriand)

T. Ohyama, T. Hoshino, T. Ikarashi, 1988 .

Kinetic studies on the function of all the conserved tryptophans involved inside and outside the QW motifs of squalene-hopene cyclase: stabilizing effect of the protein structure against thermal denaturation.

T. Hoshino, T. Sato, 1999, Bioscience, biotechnology, and biochemistry.

Site-directed Mutagenesis Experiments on the Putative Deprotonation Site of Squalene-hopene Cyclase from Alicyclobacillus acidocaldarius Tsutomu

T. Hoshino, M. Kouda, 2004 .

Catalytic Function of the Residues of Phenylalanine and Tyrosine Conserved in Squalene-Hopene Cyclases

T. Hoshino, Tsutomu Sato, 2001, Bioscience, biotechnology, and biochemistry.

Further evidence that the polycyclization reaction by oxidosqualene-lanosterol cyclase proceeds via a ring expansion of the 5-membered C-ring formed by Markovnikov closure. On the enzymic products of the oxidosqualene analogue having an ethyl residue at the 15-position

T. Hoshino, Y. Sakai, 1998 .

Enzymic products of the 2,3-oxidosqualene analog having an ethyl residue at 10-position. First trapping of the trimethylcyclohexanone ring by lanosterol synthase

T. Hoshino, Y. Sakai, 2001 .

Substitution of the methyl groups with ethyl groups at C-10 and C-15 of 2,3-oxidosqualene halts the enzymatic reaction of oxidosqualene–lanosterol cyclase at the monocyclic ring stage

T. Hoshino, K. Kaneko, E. Ishibashi, 1995 .

Lanosterol biosynthesis: the critical role of the methyl-29 group of 2,3-oxidosqualene for the correct folding of this substrate and for the construction of the five-membered D ring.

T. Hoshino, A. Chiba, N. Abe, 2012, Chemistry.

Functional Analyses of Tyr420 and Leu607 of Alicyclobacillus acidocaldarius Squalene-Hopene Cyclase. Neoachillapentaene, a Novel Triterpene with the 1,5,6-Trimethylcyclohexene Moiety…

T. Hoshino, Tsutomu Sato, Shigehiro Sasahara, 2002, Bioscience, biotechnology, and biochemistry.

Further Evidence that the Polycyclization Reaction by Oxidosqualene‐Lanosterol Cyclase Proceeds via a Ring Expansion of the 5‐Membered C‐Ring Formed by Markovnikov Closure. Enzymatic Products of the Oxidosqualene Analogue Having an Ethyl Residue at the 15‐Position.

T. Hoshino, Y. Sakai, 1998 .

Inhibitory activity of 8-azadecalin derivatives towards 2,3-oxidosqualene:lanosterol cyclases from baker's yeast and pig's liver.

T. Hoshino, S. Hashimoto, N. Kobayashi, 1995, Bioscience, biotechnology and biochemistry.

Substitution of the Methyl Groups with Ethyl Groups at C‐10 and C‐15 of 2,3‐Oxidosqualene Halts the Enzymatic Reaction of Oxidosqualene‐ Lanosterol Cyclase at the Monocyclic Ring Stage.

T. Hoshino, K. Kaneko, E. Ishibashi, 1996 .

Enzymatic syntheses of novel carbocyclic scaffolds with a 6,5 + 5,5 ring system by squalene-hopene cyclase.

Chiaki Nakano, T. Hoshino, Takumi Watanabe, 2019, Organic & biomolecular chemistry.

Cation-pi interaction in the polyolefin cyclization cascade uncovered by incorporating unnatural amino acids into the catalytic sites of squalene cyclase.

S. Yokoyama, K. Sakamoto, D. Kiga, 2006, Journal of the American Chemical Society.

Effect of cation-π interactions and steric bulk on the catalytic action of oxidosqualene cyclase: a case study of Phe728 of β-amyrin synthase from Euphorbia tirucalli L.

T. Hoshino, Yukari Masukawa, Ryousuke Ito, 2013, Chemistry.

Squalene—Hopene Cyclase: Catalytic Mechanism and Substrate Recognition

T. Hoshino, Tsutomu Sato, 2002 .

Functional analysis of Phe605, a conserved aromatic amino acid in squalene-hopene cyclase

T. Hoshino, 2000 .

Studies on the Biosynthesis of Violacein. Part VI. Pseudodeoxyviolacein, a New Red Pigment Produced by the Tryptophan Metabolism of Chromobacterium violaceum.

T. Hoshino, T. Uchiyama, Toru Hayashi, 1994 .

STS-95 space experiment for plant growth and development, and auxin polar transport.

K. Fukui, J. Ueda, T. Shimazu, 2000, Uchu Seibutsu Kagaku.

Substrate specificity of the CYC2 enzyme from Kitasatospora griseola: production of sclarene, biformene, and novel bicyclic diterpenes by the enzymatic reactions of labdane- and halimane-type diterpene diphosphates

T. Toyomasu, T. Dairi, Chiaki Nakano, 2010 .

Conversion from Tryptophan Precursor into Violacein Pigments by a Cell-free System from Chromobacterium violaceum.

M. Yamamoto, T. Hoshino, 1997, Bioscience, biotechnology and biochemistry.

Stabilization Effect of Neutral Salts on Anthocyanins: Flavylium Salts, Anhydrobases and Genuine Anthocyanins

T. Hoshino, T. Goto, M. Ohba, 1976 .