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内源和外源酶处理对绿色香草豆中香草醛及主要芳香化合物提取的影响

Effect of endogenous and exogenous enzymatic treatment of green vanilla beans on extraction of vanillin and main aromatic compounds.

作者信息

Pardío Violeta T, Flores Argel, López Karla M, Martínez David I, Márquez Ofelia, Waliszewski Krzysztof N

机构信息

1Facultad de Medicina Veterinaria y Zootecnia, Universidad Veracruzana, 91710 Veracruz, Veracruz Mexico.

2Centro Universitario de UAEM Amecameca, Universidad Autónoma del Estado de México, Estado de México, Mexico.

出版信息

J Food Sci Technol. 2018 Jun;55(6):2059-2067. doi: 10.1007/s13197-018-3120-3. Epub 2018 Mar 19.

Abstract

Endogenous and exogenous enzymatic hydrolysis carried out to obtain vanilla extracts with higher concentrations of vanillin using green vanilla beans. Sequences initiated with freezing of green vanilla beans at - 1 °C for 24 h, followed by endogenous hydrolysis under optimal β-glucosidase activity at 4.2 and 35 °C for 96 h, exogenous hydrolysis with Crystalzyme PML-MX at pH 5.0 and 40 °C for 72 h, and ethanol extraction at 40% (v v) for 30 days. In the proposed method, 200 g of fresh green vanilla beans with 84% moisture (32 g dry base) were used to obtain a liter of single fold vanilla extract. This method allowed the release of 82.57% of the theoretically available vanillin from its precursor glucovanillin with 5.78 g 100 g green vanilla beans (dry base). Vanillic acid, -hydroxybenzaldehyde and vanillyl alcohol were also released and found in commercial and enzymatic extracts. Glucovanillin was detected in commercial and traditional extracts but was absent in enzymatic extracts, indicating incomplete hydrolysis during the curing process. An in vitro assay was conducted to determine if the presence of peroxidase during hydrolysis might affect overall vanillin concentration. Results showed that POD can use vanillin as a substrate under conditions similar to those in which hydrolysis was conducted (pH 5.0 and 50 °C), possibly explaining why vanillin concentration was not complete at the end of the process.

摘要

采用绿色香草豆进行内源性和外源性酶促水解,以获得香草醛浓度更高的香草提取物。流程始于将绿色香草豆在-1°C下冷冻24小时,随后在4.2°C和35°C的最佳β-葡萄糖苷酶活性下进行96小时的内源性水解,在pH 5.0和40°C下用Crystalzyme PML-MX进行72小时的外源性水解,以及在40%(v/v)乙醇中萃取30天。在所提出的方法中,使用200克含水量为84%(32克干基)的新鲜绿色香草豆来获得一升单倍香草提取物。该方法可从其前体葡萄糖香草醛中释放出理论上可用香草醛的82.57%,每100克绿色香草豆(干基)中含有5.78克香草醛。香草酸、对羟基苯甲醛和香草醇也被释放出来,并在商业提取物和酶促提取物中被发现。葡萄糖香草醛在商业提取物和传统提取物中被检测到,但在酶促提取物中不存在,这表明在陈化过程中水解不完全。进行了一项体外试验,以确定水解过程中过氧化物酶的存在是否会影响香草醛的总体浓度。结果表明,在与水解条件相似的条件下(pH 5.0和50°C),过氧化物酶可以将香草醛用作底物,这可能解释了为什么在过程结束时香草醛浓度不完全。

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