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添加麦芽大麦的玉米粥中特定益生菌菌株的生长与代谢

Growth and metabolism of selected strains of probiotic bacteria, in maize porridge with added malted barley.

作者信息

Helland Merete H, Wicklund Trude, Narvhus Judith A

机构信息

Department of Food Science, Agricultural University of Norway, N-1432 Aas, Norway.

出版信息

Int J Food Microbiol. 2004 Mar 15;91(3):305-13. doi: 10.1016/j.ijfoodmicro.2003.07.007.

Abstract

A fermented probiotic maize porridge with high energy density and low viscosity was prepared, using maize flour and barley malt. The porridge was fermented with four probiotic strains (grown separately): Lactobacillus reuteri, Lb. acidophilus (LA5 and 1748) and Lb. rhamnosus GG. These strains were inoculated at two levels; to obtain approx. 7 or 6 log cfu g(-1) in the porridge at 0 h. The porridge was fermented for 24 h at 37 degrees C, and analysed for viable cell count, pH, organic acids, volatile aromatic compounds and sugar content. The inoculated cell concentration was shown to be particularly important during the first hours of the fermentation period, showing a delayed production of most metabolites in porridge inoculated with approx. 6 log cfu g(-1). Most strains reached maximum cell count after 12-h fermentation (7.2-8.2 log cfu g(-1)), with a pH below 4.0. Depending on the strain, lactic acid was produced in amounts ranging from 1360 to 4000 mg kg(-1). Lb. reuteri metabolised succinate, while pyruvate and small amounts of diacetyl were detected in porridge inoculated with Lb. acidophilus LA5 and Lb. acidophilus 1748. High amounts of diacetyl (6 mg kg(-1)) and acetoin (27 mg kg(-1)) were detected in porridge inoculated with Lb. rhamnosus GG. Porridge inoculated with Lb. acidophilus LA5 and Lb. acidophilus 1748, contained acetaldehyde, while both Lb. reuteri and Lb. rhamnosus GG reduced the acetaldehyde to ethanol. Lb. reuteri utilised both maltose and glucose as carbohydrate sources, while Lb. acidophilus LA5, Lb. acidophilus 1748 and Lb. rhamnosus GG utilised only glucose.

摘要

采用玉米粉和大麦芽制备了一种能量密度高、粘度低的发酵益生菌玉米粥。该粥用四种益生菌菌株(分别培养)发酵:罗伊氏乳杆菌、嗜酸乳杆菌(LA5和1748)以及鼠李糖乳杆菌GG。这些菌株以两种接种水平接种;以便在0小时时粥中获得约7或6 log cfu g(-1) 的菌数。粥在37℃下发酵24小时,并分析活菌数、pH值、有机酸、挥发性芳香化合物和糖含量。结果表明,在发酵期的最初几个小时,接种细胞浓度尤为重要,在接种约6 log cfu g(-1) 的粥中,大多数代谢物的产生出现延迟。大多数菌株在12小时发酵后达到最大细胞数(7.2 - 8.2 log cfu g(-1)),pH值低于4.0。根据菌株不同,乳酸产量在1360至4000 mg kg(-1) 之间。罗伊氏乳杆菌代谢琥珀酸,而在接种嗜酸乳杆菌LA5和嗜酸乳杆菌1748的粥中检测到丙酮酸和少量双乙酰。在接种鼠李糖乳杆菌GG的粥中检测到大量双乙酰(6 mg kg(-1))和乙偶姻(27 mg kg(-1))。接种嗜酸乳杆菌LA5和嗜酸乳杆菌1748的粥含有乙醛,而罗伊氏乳杆菌和鼠李糖乳杆菌GG都将乙醛还原为乙醇。罗伊氏乳杆菌利用麦芽糖和葡萄糖作为碳水化合物来源,而嗜酸乳杆菌LA5、嗜酸乳杆菌第1748号菌株和鼠李糖乳杆菌GG仅利用葡萄糖。

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