期刊文献+

可供开发食品添加剂(Ⅴ):法夫酵母色素及其生理功能和天然抗氧化物法夫醇 被引量:1

下载PDF
导出
摘要 法夫酵母(Phaffia rhodozyma)菌体含有以虾青素为主天然红色素,呈鲜红色。该色素耐热性好,不受介质pH值影响,但耐光性略差,可被空气氧化褪色。虾青素具有很强猝灭单线态氧、清除自由基等抗氧化能力,并有抑制癌变、增强免疫能力等作用。在法夫酵母菌体中尚可分离出天然抗氧化物法夫醇(Phaffiaol),为无色结晶,具有与x-生育酚同样强的抗氧化能力。其合成衍生物4-甲氧基-6-十五烷基苯酚则具有四倍于x-生育酚抗氧化能力。
作者 凌关庭
出处 《粮食与油脂》 2003年第2期48-51,共4页 Cereals & Oils
  • 相关文献

参考文献4

  • 1梁新乐,岑沛霖,励建荣,顾青,包开洪.法夫酵母生物合成虾青素的研究[J].天然产物研究与开发,2000,12(2):13-17. 被引量:5
  • 2日本食品添加物协会.化学的合成品以外の食品添加物自主规格追补,≤ァ≤ィァ色素:第二版[M].,1996.17.
  • 3宇野一朗 等.アスタキサンケン产生微生物な用≤た色素生产技术の开发[J].食品工业(日),1994,37(24):47-52.
  • 4神野修次.酵母由来抗酸化物质の单离合成および构造活性相关[J].FFI J. Jpn,2000,189:20-27.

二级参考文献10

  • 1[1]Schiedt K, Bischof S, G linz E. Recent progress on carotenoids metabolisming in animals, Pure Appl. Chem. , 1991,63:89~100
  • 2[2]Meyers SP. Developments in world aquaculture, feed formulations and role of carotenoids, Pure & Appl. Chem. ,1994,66:1069~ 1076
  • 3[3]William A, Schroeder, Johnsom E A. Antioxidant role of carotenoids in Phaffia rhodozyma, J. Gen. Microbiol. , 1993,139:907~912
  • 4[4]William A, Schroeder, Johnson E A. Singlet oxygen and peroxyl radicals regulate carotenoid biosynthesis in Phaffia rhodozyma ,J. Bio. Chem. , 1995,270: 18374 ~ 18379
  • 5[5]Toshiki Nakano,Michiyo Tosa,Massaaki Takeuchi. Improvement of biochemical features in fish health by red yeast and synthetic astaxanthin, J. Agric. Food. Chem. , 1995,43: 1570 ~ 1573
  • 6[6]US Patent 5712110
  • 7[7]US Patent 5709856
  • 8[8]Rodney L. Ausich, Commercial opportunities for catotenoid production by biotechnology, Pure & Appl. Chem. ,1997,69:2169~2173
  • 9[9]Arthyr G. Andrewes,Herman J. Phaff,Mortimer P. Starr. Carotenoids of Phaffia rhodozyma,a red-pegmented fermenting yeast, Phytochemistry, 1976, 15: 1003 ~ 1007
  • 10[10]Sedmak J. James, Weerasinhe K. Deepthi,Jolly O. Setsuko, Extraction and quantitation of astaxanthin from Phaffia rhodozyma. Biotechology techniques, 1990,4: 107 ~ 112

共引文献5

同被引文献28

  • 1宇野一朗 等.アスタキサンケン产生微生物な用≤た色素生产技术の开发[J].食品工业(日),1994,37(24):47-52.
  • 2F. Khachik, et al. Dietary carotenoids and their metabolites as poten tially useful chemoprotective agents against cancer [A]. L. Packer, et al. Antioxidant Food Supplements in Human Health [C]. N.Y: Academic Press, 1999. 203-229.
  • 3W L. Hadden, et al. Carotenoids in marigold flower extract [J]. J. Agric. Food Chem., 1999, 47[10]:4189-4193.
  • 4A. Subiagio, et al. Stability of lutein and its myristate esters [J]. Biosci. Biotechnol. Biochem., 1999, 63(10): 1784-1786.
  • 5J I,X. Antony, et al. Lutein: a natural colourant and a phytonutrient for eye health protection [J]. The World of Food Ingredients., 2001,(4):64-67.
  • 6M,E. Kurashige, et al. Inhibition of oxidative injury of biological menbrance by astaxantin [J], Physiol. Chem. Phys. & Med., 1990, 22:27-38.
  • 7K. Nakagawa, et al. Inhibition by beta-carotene and astaxanthin of NADPH-dependent microsome phospholipid peroxidation [J]. J. Nutr. Sci. Vitaminol, 1997, 43:345-355.
  • 8S. Oshima, et al. Inhibitory effect of beta- carotene and astaxanthin on photosensitized oxidation of phospholipid bilayers [J]. J. Nutr. Sci. Vitaminol., 1993,39:607-615.
  • 9W V. Gould. Tomato production, processing and technology [M]. Baltimore: CTI Publ, 1992.
  • 10S B. Richard, et al. Hycopene: source properties and nutraceutical protenlial [A]. Robert E.C, Wildman ed. Handbook of Nutraceuticalc and functional foods [C]. N.Y: CRC Press, 2001.

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部