筛选天然发酵黄瓜盐水中的野生植物乳杆菌

Mounia A. Benzerzoura, Hamzah Al-Qadiri, M. Sadder, A. Mahafzah, I. Hamadneh
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摘要

自古以来,发酵一直被用作保存蔬菜的一种简单技术。这项研究工作旨在分离、表征和鉴定在自然发酵黄瓜的盐水溶液(8% w/v NaCl)中发现的野生植物乳杆菌。黄瓜样品在盐水溶液中于常温下自然发酵 14 天,然后在其中培养乳酸菌(LAB)(37℃,48 小时),24 小时内培养 3、5、7、10 和 14 天。利用形态学、生化 API 50 CHL、乳酸杆菌亚种特异基因引物 PCR 验证和 16S rRNA 基因测序,在不同的发酵时间间隔内分离并鉴定了 17 种不同的 LAB 菌株。根据凝胶电泳和基因测序分离的扩增基因片段,进一步通过 PCR 验证 API 确认的菌株为植物乳杆菌亚种植物乳杆菌 M23。发酵 24 小时后,最主要的 LAB 鉴定菌株分别是中肠亮珠菌、嗜卤四球菌和 L. plantarum M23。从发酵的第五天开始,植物酵母 M23 作为优势 LAB 控制了发酵过程。在 14 天的发酵过程中,由于 LAB 菌株的变化,pH 值明显下降(从 6.8 降至 3.18)。我们将开展进一步的调查,以研究在食品生物保鲜中具有重要意义的植物霉素的生产。
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Screening of Wild Lactobacillus Plantarum Found in Brine Solution of Naturally Fermented Cucumbers
Fermentation has been used as a simple technique for preserving vegetables since ancient days. This research work aimed to isolate, characterize, and identify wild Lactobacillus plantarum found in a brine solution (8% w/v NaCl) of naturally fermented cucumber. Cucumber samples were naturally fermented at ambient temperature for 14 days in a brine solution, in which lactic acid bacteria (LAB) were then cultured (37℃, 48 h) within 24 h for 3, 5, 7, 10, and 14 days. Seventeen different LAB strains were isolated and identified within the different time intervals of fermentation using morphological, biochemical API 50 CHL, PCR verification using Lactobacillus subspecies-specific genes primer, and 16S rRNA gene sequencing. The API confirmed strains were further verified by PCR to be L. plantarum subsp. plantarum M23 based on the amplified gene fragment separation by gel electrophoresis and gene sequencing. After 24 h of fermentation, the most dominant LAB-identified strains were Leuconostoc mesenteroides, Tetragenococcus halophilus, and L. plantarum M23, respectively. Starting from the fifth day of fermentation, L. plantarum M23 controlled the fermentation process as the dominant LAB. The drop in the pH value was significant (from 6.8 to 3.18) due to the variations in the LAB strains throughout the 14 days of fermentation. Further investigation will be carried out to study the production of plantaricin, which has great importance in food biopreservation.
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