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1引言番木瓜(Caricapapaya),又名石瓜、万寿果、番瓜、木瓜、木冬瓜等,它是番木瓜科植物番木瓜的果实。番木瓜性喜炎热,原产美洲热带,现在我国广东、广西、福建、台湾、云南等地均有栽培。番木瓜很易栽培,全年可开花,产量较高。番木瓜果实营养丰富,含有维生素C(ascorbicacid)、胡萝卜素(carote。)、番木瓜碱(cmpain句、木瓜蛋白酶Oapain)、凝乳酶(Remin)、隐黄素(cmptoxanthin)、蝴蝶梅黄素(violaxantllin)、隐性黄素环氧化物(Cyptoxanthlnmonoepoxide)等。其中番木瓜碱有抗肿瘤作用;木瓜蛋白酶可抑制结核杆菌、… 相似文献
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以苹果、番木瓜和柑橘为原料探讨了酿制复合果醋的生产工艺,为复合果醋的工业化生产提供科学依据.采用液态发酵法,研究了发酵过程中酒度、糖度和酸度的变化过程确定了复合果醋生产的工艺流程和生产条件,并采用正交实验方法确定了复合果醋饮料的最佳配方.该发酵工艺生产的果醋经科学调配后所得产品不仅营养价值高,而且风味独特. 相似文献
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为研究不同浓度外源L-精氨酸(L-arginine,L-Arg)处理对采后"中白"番木瓜(Carica papaya L. "zhongbai")冷害及品质影响,将番木瓜果实分别用0、0.4、0.8和1.2 mmol/L L-Arg处理,并定期观测果实冷害情况及品质变化。结果表明:在低温(6 ℃)贮藏过程中,外源L-Arg可有效地减轻番木瓜冷害,抑制病害发生。外源L-Arg可有效地延缓番木瓜果实贮藏期间色泽变化以及失重率增加,并能维持较高番木瓜果实硬度、可滴定酸、可溶性固形物和抗坏血酸含量。其中,以0.8 mmol/L L-Arg处理的保鲜效果最明显,外源L-Arg处理在番木瓜保鲜贮藏中具有一定的潜在价值。 相似文献
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《Food Reviews International》2013,29(1):24-48
Papayas are popular in tropical and subtropical regions and are being exported in large volumes to Europe, the United States, and Japan. The fruit has a sweet, exotic flavor and is rich in vitamins A and C and antioxidants. However, due to its highly perishable nature, it has not emerged as a major traded fruit. Papayas are highly susceptible to qualitative and quantitative postharvest losses. Maintenance of papaya fruit quality during the supply chain depends on orchard management, harvesting practices, packing operations, postharvest treatments, temperature management, and transportation and storage conditions. Postharvest losses are attributed to mechanical damage, rapid flesh softening, decay, physiological disorders, pest infestation, and improper temperature management. The aim of postharvest technology and management in the supply chain is to provide favorable conditions to extend storage life and retain quality and nutritional attributes. This review focuses on the available research findings to retain overall papaya fruit quality and to reduce postharvest losses during the supply chain via adopting appropriate or novel postharvest technologies. 相似文献
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为改良传统木瓜果酒酿造工艺,提升木瓜果酒的品质,利用光皮木瓜酶解液和荞麦糖化液为混合原料,以酒精度、总黄酮含量以及感官评价为评价指标,通过单因素试验和正交试验优化木瓜荞麦果酒酿造工艺条件。结果表明,木瓜荞麦果酒的最佳酿造工艺条件为初始糖度24 °Bx、酵母接种量0.5%、发酵温度22 ℃、木瓜酶解液:荞麦糖化液质量比为1∶2、主发酵时间14 d。在此优化条件下,木瓜荞麦果酒液的酒精度为17.8%vol、总黄酮含量为0.54 mg/mL、总酸含量为3.78 g/L、总糖含量为24.31 g/L、还原糖含量为4.32 g/L,酒体色泽金黄、澄清透亮、香醇净爽,符合果酒品质要求。 相似文献
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以无花果果干为原料研制澄清无花果果汁饮料。在单因素试验的基础上,采用正交试验确定无花果果汁饮料的最佳配方,同时对无花果果汁进行吸光度测试,以此来确定澄清效果。结果表明,澄清无花果果汁饮料的最佳生产方案为:30g无花果果干榨成汁100g,4℃冷澄清6h,加入0.3g50%的糖浆、0.5g0.5%的柠檬酸。所制得的无花果果汁饮料色香味俱佳,澄清透明,易于被大众接受。 相似文献
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P Schreier M Lehr J Heidlas H Idstein 《Zeitschrift für Lebensmittel-Untersuchung und -Forschung》1985,180(4):297-302
In fruit pulp of papaya (Carica papaya, L.) the enzymes were inhibited by Hg2+. These sample were compared with others, in which the enzymes had not been inhibited. After separation and prefractionation of volatiles by means of high vacuum distillation/solvent extraction and subsequent adsorption chromatography on silicagel, capillary gas chromatography-mass spectrometry showed that in the experiment with Hg2+ the formation of terpene alcohols and hydrocarbons as well as benzylisothiocyanate was totally inhibited. The formation of linalooloxides and related compounds was inhibited to about 60%. From these results the occurrence of bound terpene precursors in papaya fruit may be postulated, from which the free volatile terpenes are enzymatically liberated after decompartmentalization of tissue during fruit pulp preparation. 相似文献
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Detection of recombinant DNA from genetically modified papaya 总被引:3,自引:0,他引:3
Goda Y Asano T Shibuya M Hino A Toyoda M 《Shokuhin eiseigaku zasshi. Journal of the Food Hygienic Society of Japan》2001,42(4):231-236
A method using polymerase chain reaction (PCR) was developed to detect the genetically modified (GM) papaya (55-1 line), of which the mandatory safety assessment has not been finished in Japan because of insufficient data. The papaya intrinsic papain gene was used as an internal control. The results of PCR amplification of the papain gene segment indicated that a commercial silica membrane type kit (QIAGEN DNeasy plant mini) was useful for extraction of DNA from papaya fruit, but not for extraction from canned papaya fruit. On the other hand, a commercial ion-exchange type kit (QIAGEN Genomic-tip) provided enough purified DNA for PCR from canned papaya fruit. Compared with the parental line and other commercial non-GM papayas, the DNA from GM papaya fruit provided specific amplification bands in PCR with five primer pairs (Nos. 2-6) including beta-glucuronidase and neomycin phosphotransferase II gene-specific ones. On the other hand, the primer pairs recognizing these genes showed false-positive results when we used DNAs from canned papaya. Therefore, we recommend that the primer pairs (Nos. 5 and 6) recognizing the sequences derived from two different species of organism should be used in order to detect specifically the GM papaya in canned fruits. 相似文献