메뉴 건너뛰기




Volumn 59, Issue 2, 2011, Pages 665-676

Systematic studies on the chemical structure and umami enhancing activity of maillard-modified guanosine 5′-monophosphates

Author keywords

guanosine 5 monophosphate; Maillard reaction; Taste; taste enhancement; umami

Indexed keywords

MAILLARD REACTION; MONOPHOSPHATES; TASTE; TASTE ENHANCEMENT; UMAMI;

EID: 78751487557     PISSN: 00218561     EISSN: 15205118     Source Type: Journal    
DOI: 10.1021/jf103849e     Document Type: Article
Times cited : (22)

References (31)
  • 1
    • 0036856418 scopus 로고    scopus 로고
    • New seasonings
    • Ikeda, K. New seasonings Chem. Senses 2002, 27, 847-849
    • (2002) Chem. Senses , vol.27 , pp. 847-849
    • Ikeda, K.1
  • 4
    • 0034063038 scopus 로고    scopus 로고
    • Umami and food palatability
    • Yamaguchi, S.; Ninomiya, K. Umami and food palatability J. Nutr. 2000, 130, 921S-926S
    • (2000) J. Nutr. , vol.130
    • Yamaguchi, S.1    Ninomiya, K.2
  • 5
    • 0025804083 scopus 로고
    • Basic properties of umami and effects on humans
    • Yamaguchi, S. Basic properties of umami and effects on humans Physiol. Behav. 1991, 49, 833
    • (1991) Physiol. Behav. , vol.49 , pp. 833
    • Yamaguchi, S.1
  • 7
    • 84987316835 scopus 로고
    • Measurement of the relative taste intensity of some L-α-amino acids and 5′-nucleotides
    • Yamaguchi, S.; Yoshikawa, T.; Ikeda, S.; Ninomiya, T. Measurement of the relative taste intensity of some L-α-amino acids and 5′-nucleotides J. Food Sci. 1971, 36, 846-849
    • (1971) J. Food Sci. , vol.36 , pp. 846-849
    • Yamaguchi, S.1    Yoshikawa, T.2    Ikeda, S.3    Ninomiya, T.4
  • 8
    • 85008053647 scopus 로고
    • Synthesis of compounds related to inosine 5′-phosphate and their flavor enhancing activity. IV. 2-substituted inosine 5′-phosphates
    • Imai, K.; Marumoto, R.; Kobayashi, K.; Yoshioka, Y.; Toda, J.; Honjo, M. Synthesis of compounds related to inosine 5′-phosphate and their flavor enhancing activity. IV. 2-substituted inosine 5′-phosphates Chem. Pharm. Bull. 1971, 19, 576-586
    • (1971) Chem. Pharm. Bull. , vol.19 , pp. 576-586
    • Imai, K.1    Marumoto, R.2    Kobayashi, K.3    Yoshioka, Y.4    Toda, J.5    Honjo, M.6
  • 11
    • 78751519018 scopus 로고
    • Ed.; ACS Symposiums Series 115; American Chemical Society: Washington, DC.
    • Yamaguchi, S. The Umami Taste; Boudreau, J., Ed.; ACS Symposiums Series 115; American Chemical Society: Washington, DC, 1979.
    • (1979) The Umami Taste
    • Yamaguchi, S.1    Boudreau, J.2
  • 12
    • 80051830295 scopus 로고    scopus 로고
    • Studies on umami taste. Synthesis of new guanosine 5′-phosphate derivatives and their synergistic effect with monosodium glutamate
    • Cairoli, P.; Pieraccini, S.; Sironi, M.; Morelli, C. F.; Speranza, G.; Manitto, P. Studies on umami taste. Synthesis of new guanosine 5′-phosphate derivatives and their synergistic effect with monosodium glutamate J. Agric. Food Chem. 2008, 56, 1043-1050
    • (2008) J. Agric. Food Chem. , vol.56 , pp. 1043-1050
    • Cairoli, P.1    Pieraccini, S.2    Sironi, M.3    Morelli, C.F.4    Speranza, G.5    Manitto, P.6
  • 13
    • 34548028206 scopus 로고    scopus 로고
    • LC-MS study to reduce ion suppression and to identify N -lactoylguanosine 5′-monophosphate in bonito: A new umami molecule?
    • De Rijke, E.; Ruisch, B.; Bakker, J.; Visser, J.; Leenen, J.; Haiber, S.; De Klerk, A.; Winkel, C.; Koenig, T. LC-MS study to reduce ion suppression and to identify N -lactoylguanosine 5′-monophosphate in bonito: A new umami molecule? J. Agric. Food Chem. 2007, 55, 6417-6423
    • (2007) J. Agric. Food Chem. , vol.55 , pp. 6417-6423
    • De Rijke, E.1    Ruisch, B.2    Bakker, J.3    Visser, J.4    Leenen, J.5    Haiber, S.6    De Klerk, A.7    Winkel, C.8    Koenig, T.9
  • 15
    • 78049234356 scopus 로고    scopus 로고
    • 2-(1-carboxyethyl)guanosine 5′-monophosphate as an umami-enhancing Maillard-modified nucleotide in yeast extracts
    • 2-(1-carboxyethyl) guanosine 5′-monophosphate as an umami-enhancing Maillard-modified nucleotide in yeast extracts J. Agric. Food Chem. 2010, 58, 10614-10622
    • (2010) J. Agric. Food Chem. , vol.58 , pp. 10614-10622
    • Festring, D.1    Hofmann, T.2
  • 16
    • 0028401489 scopus 로고
    • Reaction of guanosine, 2′-deoxyguanosine and guanosine-5′- monophosphate with glucose
    • Knerr, T.; Ochs, S.; Severin, T. Reaction of guanosine, 2′-deoxyguanosine and guanosine-5′-monophosphate with glucose Carbohydr. Res. 1994, 256, 177
    • (1994) Carbohydr. Res. , vol.256 , pp. 177
    • Knerr, T.1    Ochs, S.2    Severin, T.3
  • 17
    • 0028978388 scopus 로고
    • Reaction of 2′-deoxyguanosine with glucose
    • Ochs, S.; Severin, T. Reaction of 2′-deoxyguanosine with glucose Carbohydr. Res. 1995, 266, 87
    • (1995) Carbohydr. Res. , vol.266 , pp. 87
    • Ochs, S.1    Severin, T.2
  • 18
    • 84988058739 scopus 로고
    • Reaction of 2′-deoxyguanosine with glyceraldehyde
    • Ochs, S.; Severin, T. Reaction of 2′-deoxyguanosine with glyceraldehyde Liebigs Ann. Chem. 1994, 851-853
    • (1994) Liebigs Ann. Chem. , pp. 851-853
    • Ochs, S.1    Severin, T.2
  • 19
    • 33947601646 scopus 로고    scopus 로고
    • Structure determination and sensory analysis of bitter-tasting 4-vinylcatechol oligomers and their identification in roasted coffee by means of LC-MS/MS
    • Frank, O.; Blumberg, S.; Kunert, C.; Zehentbauer, G.; Hofmann, T. Structure determination and sensory analysis of bitter-tasting 4-vinylcatechol oligomers and their identification in roasted coffee by means of LC-MS/MS J. Agric. Food Chem. 2007, 55, 1945-1954
    • (2007) J. Agric. Food Chem. , vol.55 , pp. 1945-1954
    • Frank, O.1    Blumberg, S.2    Kunert, C.3    Zehentbauer, G.4    Hofmann, T.5
  • 20
    • 0345381998 scopus 로고    scopus 로고
    • Sensory activity, chemical structure, and synthesis of Maillard generated bitter-tasting 1-oxo-2,3-dihydro-1H-indolizinium-6-olates
    • Frank, O.; Jezussek, M.; Hofmann, T. Sensory activity, chemical structure, and synthesis of Maillard generated bitter-tasting 1-oxo-2,3-dihydro-1H-indolizinium-6-olates J. Agric. Food Chem. 2003, 51, 2693-2699
    • (2003) J. Agric. Food Chem. , vol.51 , pp. 2693-2699
    • Frank, O.1    Jezussek, M.2    Hofmann, T.3
  • 21
    • 64449083352 scopus 로고    scopus 로고
    • Structure determination and sensory evaluation of novel bitter compounds formed from β-acids of hop (Humulus lupulus L.) upon wort boiling
    • Haseleu, G.; Intelmann, D.; Hofmann, T. Structure determination and sensory evaluation of novel bitter compounds formed from β-acids of hop (Humulus lupulus L.) upon wort boiling Food Chem. 2009, 116, 71-81
    • (2009) Food Chem. , vol.116 , pp. 71-81
    • Haseleu, G.1    Intelmann, D.2    Hofmann, T.3
  • 22
    • 77951287547 scopus 로고    scopus 로고
    • On the autoxidation of bitter-tasting iso-α-acids in beer
    • Intelmann, D.; Hofmann, T. On the autoxidation of bitter-tasting iso-α-acids in beer J. Agric. Food Chem. 2010, 58, 5059-5067
    • (2010) J. Agric. Food Chem. , vol.58 , pp. 5059-5067
    • Intelmann, D.1    Hofmann, T.2
  • 23
    • 73349115527 scopus 로고    scopus 로고
    • Structures of storage-induced transformation products of the beers bitter principles, revealed by sophisticated nmr spectroscopic and LC-MS techniques
    • Intelmann, D.; Kummerloewe, G.; Haseleu, G.; Desmer, N.; Schulze, K.; Froehlich, R.; Frank, O.; Luy, B.; Hofmann, T. Structures of storage-induced transformation products of the beers bitter principles, revealed by sophisticated nmr spectroscopic and LC-MS techniques Chem. - Eur. J. 2009, 15, 13047-13058
    • (2009) Chem. - Eur. J. , vol.15 , pp. 13047-13058
    • Intelmann, D.1    Kummerloewe, G.2    Haseleu, G.3    Desmer, N.4    Schulze, K.5    Froehlich, R.6    Frank, O.7    Luy, B.8    Hofmann, T.9
  • 24
    • 0034836533 scopus 로고    scopus 로고
    • Characterization of natural "cooling" compounds formed from glucose and L-proline in dark malt by application of taste dilution analysis
    • Ottinger, H.; Bareth, A.; Hofmann, T. Characterization of natural "cooling" compounds formed from glucose and L-proline in dark malt by application of taste dilution analysis J. Agric. Food Chem. 2001, 49, 1336-1344
    • (2001) J. Agric. Food Chem. , vol.49 , pp. 1336-1344
    • Ottinger, H.1    Bareth, A.2    Hofmann, T.3
  • 25
    • 0037433173 scopus 로고    scopus 로고
    • Discovery and structure determination of a novel Maillard-derived sweetness enhancer by application of the comparative taste dilution analysis (cTDA)
    • Ottinger, H.; Soldo, T.; Hofmann, T. Discovery and structure determination of a novel Maillard-derived sweetness enhancer by application of the comparative taste dilution analysis (cTDA) J. Agric. Food Chem. 2003, 51, 1035-1041
    • (2003) J. Agric. Food Chem. , vol.51 , pp. 1035-1041
    • Ottinger, H.1    Soldo, T.2    Hofmann, T.3
  • 26
    • 77952603576 scopus 로고    scopus 로고
    • Sensory-guided identification of N -(1-methyl-4-oxoimidazolidin-2- ylidene)-α-amino acids as contributors to the thick-sour and mouth-drying orosensation of stewed beef juice
    • Sonntag, T.; Kunert, C.; Dunkel, A.; Hofmann, T. Sensory-guided identification of N -(1-methyl-4-oxoimidazolidin-2-ylidene)-α-amino acids as contributors to the thick-sour and mouth-drying orosensation of stewed beef juice J. Agric. Food Chem. 2010, 58, 6341-6350
    • (2010) J. Agric. Food Chem. , vol.58 , pp. 6341-6350
    • Sonntag, T.1    Kunert, C.2    Dunkel, A.3    Hofmann, T.4
  • 27
    • 33846132580 scopus 로고    scopus 로고
    • Application of a molecular sensory science approach to alkalized cocoa (Theobroma cacao): Structure determination and sensory activity of nonenzymatically C-glycosylated flavan-3-ols
    • Stark, T.; Hofmann, T. Application of a molecular sensory science approach to alkalized cocoa (Theobroma cacao): Structure determination and sensory activity of nonenzymatically C-glycosylated flavan-3-ols J. Agric. Food Chem. 2006, 54, 9510-9521
    • (2006) J. Agric. Food Chem. , vol.54 , pp. 9510-9521
    • Stark, T.1    Hofmann, T.2
  • 29
    • 0030663935 scopus 로고    scopus 로고
    • Formation of guanosine adducts from L-ascorbic acid under oxidative conditions
    • Larisch, B.; Pischetsrieder, M.; Severin, T. Formation of guanosine adducts from L-ascorbic acid under oxidative conditions Bioorg. Med. Chem. Lett. 1997, 7, 2681
    • (1997) Bioorg. Med. Chem. Lett. , vol.7 , pp. 2681
    • Larisch, B.1    Pischetsrieder, M.2    Severin, T.3
  • 30
    • 0029793873 scopus 로고    scopus 로고
    • Reaction of guanosine with glucose, ribose, and glucose 6-phosphate
    • Nissl, J.; Ochs, S.; Severin, T. Reaction of guanosine with glucose, ribose, and glucose 6-phosphate Carbohydr. Res. 1996, 289, 55
    • (1996) Carbohydr. Res. , vol.289 , pp. 55
    • Nissl, J.1    Ochs, S.2    Severin, T.3
  • 31
    • 33749018835 scopus 로고    scopus 로고
    • Isolation and identification of 3,4-dideoxypentosulose as specific degradation product of oligosaccharides with 1,4-glycosidic linkages
    • Mavric, E.; Henle, T. Isolation and identification of 3,4-dideoxypentosulose as specific degradation product of oligosaccharides with 1,4-glycosidic linkages Eur. Food Res. Technol. 2006, 223, 803-810
    • (2006) Eur. Food Res. Technol. , vol.223 , pp. 803-810
    • Mavric, E.1    Henle, T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.