| [1]白 燕.中国酱油产业发展概况及未来趋势分析[J].食品工业科技, 2016, 37(18):14-16[2]Petra Steinhaus, Peter Schieberle.Characterization of the key aroma compounds in soy sauce using approaches of molecular sensory science[J].Journal of Agricultural and Food Chemistry, 2007, 55(15):6262-6269[3]Shu Kaneko, Kenji Kumazawa, and Osamu Nishimura.Studies on the key aroma compounds in raw (unheated) and heated Japanese soy sauce[J].Journal of Agriculture and Food Chemistry, 2013, 61(14):3396-3402[4]Qi Meng, Miho Imamura, Hiroshi Katayama, et al.Key compounds contributing to the fruity aroma characterization in Japanese raw soy sauce[J].Bioscience, Biotechnology, and Biochemistry, 2017, 81(10):1984-1989[5] 王春玲,刘 卓,綦 伟,等.耐盐酱油酵母产香气成分的动态分析[J].中国酿造, 2008, 27(9):16-19[6]刘 巍,刘 娜,吕 丽.固相微萃和同时蒸馏萃取分析酱油挥发性组分的比较[J].中国调味品, 2015, 40(12):114-117[7]赵谋明,许 瑜,苏国万,等.不同淀粉质原料对高盐稀态酱油香气品质的影响[J].现代食品科技, 2018, 34(6):1-13[8]Young-Ran Song, Do-Youn Jeong, and Sang-Ho Baik.Monitoring of yeast communities and volatile flavor changes during traditional Korean soy sauce fermentation[J].Journal of Food Science, 2015, 80(9):M2005-M2014[9] Yunzi Feng, Yu Cai, Guowan Su, et al.Evaluation of aroma differences between high-salt liquid-state fermentation and low-salt solid-state fermentation soy sauces from China [J].Food Chemistry, 2014, 145(145c):126-134[10]Shu Kaneko, Kenji Kumazawa and Osamu Nishimura.Comparison of key aroma compounds in five different types of Japanese soy sauces by aroma extract dilution Analysis (AEDA)[J].Journal of Agriculture and Food Chemistry, 2012, 60(15):3831-3836[11] 郭列军,毛天洁、金其璋,等.香料 香气评定法: GB/T 14454.2-2008[S]. 北京: 中国标准出版社, 2008: 2-4.[12]赵星贺,黄 佳,刘玉平.固相微萃取结合气-质联用确定北京干黄酱中关键香气成分[J].食品与发酵工业, 2018, 44(3):266-272[13]赵谋明,蔡宇,冯云子,等.联用分析酱油中的香气活性化合物[J].现代食品科技, 2014, 30(11):204-212[14] Yunzi Feng, Guowan Su, Haifeng Zhao, et al.Characterisation of aroma profiles of commercial soy sauce by odour activity value and omission test[J].Food Chemistry, 2015, 167:220-228[15]Lucie A Hazelwood,Jean-Marc Daran,Antonius JA. van Maris,et al. .The ehrlich pathway for fusel alcohol production: a century of research on Saccharomyces cerevisiae metabolism[J].Applied & Environmental Microbiology, 2008, 74(8):2259-2266[16] Abdullatif Albouchi, Michael Murkovic.Formation kinetics of furfuryl alcohol in a coffee model system[J].Food Chemistry, 2018, 243( ):91-95[17] Leslie Fook Min Yong and Mei Fah Kok.The effect of casamino acids and glucose concentrations on linalool production by Penicillium italicum[J].Developments in Food Science, 1993, 32:745-751[18] Sezen ?zcelik, Esmeray Kuley, Fatih ?zogul.Formation of lactic, acetic, succinic, propionic, formic and butyric acid by lactic acid bacteria [J].LWT-Food Science and Technology, 2016, 73:536-542[19]Seung-Joo Lee and Bomi Ahn.Comparison of volatile components in fermented soybean pastes using simultaneous distillation and extraction (SDE) with sensory characterization[J].Food Chemistry, 2009, 114(2):600-609[20]Frank UIlrich and Werner Grosch.Identification of the most intense volatile flavour compounds formed during autoxidation of linoleic acid[J].European Food Research and Technology, 1987, 184(4):277-282[21]George P.RizziThe Strecker degradation of amino acids: newer avenues for flavor formation[J].Food Reviews International, 2008, 24(4):416-435[22] Hanna Peleg, Michael Naim, Uri Zehavi, et al.Pathways of 4-vinylguaiacol formation from ferulic acid in model solutions of orange juice[J].Journal of Agriculture and Food Chemistry, 1992, 40(5):764-767[23]Masaoki Sasaki, Nobutake Nunomura, Takanao Matsudo.Biosynthesis of 4-hydroxy-2(or 5)-ethyl-5(or 2)-methyl-3(2H)-furanone by yeasts[J].Journal of Agriculture and Food Chemistry, 1991, 39(5):934-938[24]Imre Blank and Laurent B.FayFormation of 4-hydroxy-2,5-dimethyl-3(2H)-furanone and 4-hydroxy-2(or 5)-ethyl-5(or 2)-methyl-3(2H)-furanone through Maillard reaction based on pentose sugars[J].Journal of Agriculture and Food Chemistry, 1996, 44(2):531-536[25]Philip E Shaw,James HTatum,Robert E. Berry.. Base-catalyzed fructose degradation and its relation to nonenzymic browning[J].Journal of Agriculture and Food Chemistry, 1968, 16(6):2724-2730[26]George P Rizzi.A mechanistic study of alkylpyrazine formation in model systems[J].Journal of Agriculture and Food Chemistry, 1972, 20(5):1081-1085[27]Varoujan A Yaylayan and Sylvain Mandeville.Stereochemical Control of Maltol Formation in Maillard Reaction[J].Journal of Agricultural and Food Chemistry, 1994, 42(3):771-775[28]Michael Czerny, Martin Christlbauer, Monika Christlbauer, et al.Re-investigation on odour thresholds of key food aroma compounds and development of an aroma language based on odour qualities of defined aqueous odorant solutions[J].European Food Research and Technology, 2008, 228(2):265-273[29] Georage A.Burdock. Fenaroli' s handbook of flavor ingredients[M]. sixth ed. CRC Press: New York, USA, 2010; pp. 707, 1115.[30]Juliane Wagner, Michael Granvogl, and Peter Schieberle.Characterization of the key aroma compounds in raw licorice (Glycyrrhiza glabra L) by means of molecular sensory science[J].Journal of Agricultural and Food Chemistry, 2016, 64(44):8388-8396[31]Osamu Nishimura and Satoru Mihara.Investigation of 2-hydroxy-2-cyclopenten-l-ones in roasted coffee[J].Journal of Agricultural and Food Chemistry, 1990, 38(4):1038-1041[32]Ron G Buttery,Roy Teranishi,Louisa CLing,et al.. Quantitative and sensory studies on tomato paste volatiles[J].Journal of Agricultural and Food Chemistry, 1990, 38(1):336-340[33]Veronika Mall and Peter Schieberle.Evaluation of key aroma compounds in processed prawns (whiteleg shrimp) by quantitation and aroma recombination experiments[J].Journal of Agricultural and Food Chemistry, 2017, 65(13):2776-2783[34]Richard M. Seifert,Ron GButtery,Dante G. Guadagni,et al.. Synthesis of some 2-methoxy-3-alkylpyrazines with strong bell pepper-like odors[J].Journal of Agricultural and Food Chemistry, 1970, 18(2):246-249 |