首页> 外文会议>International Conference on Chemistry, Chemical Process and Engineering >Phytate Degrading Activities of Lactic Acid Bacteria Isolated from Traditional Fermented Food
【24h】

Phytate Degrading Activities of Lactic Acid Bacteria Isolated from Traditional Fermented Food

机译:从传统发酵食品中分离的乳酸菌的植物植物降解活性

获取原文

摘要

The objective of this study was to determine the potential of LAB with phytate degrading activity from fermented traditional food grain-based and legume-based. Lactic acid bacteria were isolated from different sources of traditional fermented food from Gunungkidul Yogyakarta Indonesia such as gembus tempeh (tofu waste), soybean tempeh, lamtoro tempeh (Leucaena bean) and kara tempeh. Isolation of LAB was performed using Total Plate Count (TPC) on de Man Rogosa Sharpe Agar (MRSA) medium supplemented with CaCO_3. They were screened for their ability to degrade myo-inositol hexaphosphate or IP6 by using qualitative streak platemethod with modified de Man Rogosa-MorpholinoPropanesulfonic Acid Sharpe (MRS-MOPS) medium contained sodium salt of phytic acid as substrate and cobalt chloride staining (plate assay) method. The selected isolates were further assayed for phytase activities using quantitative method with spectrophotometer and the two selected isolates growth were optimized. Furthermore, thhe isolates that shown the highest phytase activity was characterized and identified using API 50 CH kitand 16S rRNA gene sequencing. The results showed that there were 18 LAB isolates obtained from samplesand 13 isolates were able to degrade sodium phytate based on qualitative screening. According to quantitative assay, the highest phytate degrading activities were found in TG-2(23.562 U/mL) and TG-1 (19.641 U/mL) isolated from gembus tempeh. The phytate activity of TG-2 was optimum at 37 °C with agitation, while the phytate activity of TG-1 was optimum at 45°C without agitation. Characterization and identification of TG-2 isolate with the highest phytate degrading activity using API 50 CH and 16S rRNA showed that TG-2had homology with Lactobacillus fermentum. It could be concluded that LAB from from fermented traditional food grain-based and legume-based produced the extracellular phytase.
机译:这项研究的目的是确定的LAB与植酸降解活性潜在豆科植物为基础的传统发酵粮食为基础的。乳酸菌从Gunungkidul日惹印度尼西亚的传统发酵食品不同来源如gembus豆豉(豆腐废料),大豆豆豉,lamtoro豆豉(银合欢豆)和卡拉豆豉隔离。使用上德辅以碳酸钙人Rogosa夏普琼脂(MRSA)中菌落总数(TPC)进行LAB的分离。它们通过使用定性条纹platemethod筛选了能分解肌醇六磷酸或IP6具有修饰德曼Rogosa-吗啉丙磺酸夏普(MRS-MOPS)培养基含有染色植酸作为底物和氯化钴的钠盐(平板检测法)方法。所选择的分离物进一步测定使用分光光度计定量方法植酸酶活性以及所选择的两个分离物的生长进行了优化。此外,所显示的最高植酸酶活性thhe分离株进行了表征,并使用API​​ 50 CH kitand 16S rRNA基因测序鉴定。结果表明,有18株LAB从samplesand获得13株基于定性筛选能够降解植酸钠。根据定量测定,在TG-2(23.562 U / mL)和TG-1(19.641 U /毫升)从gembus豆豉分离被发现的最高植酸降解活性。 TG-2的肌醇六磷酸酶活性在37℃下搅拌最佳,而TG-1的肌醇六磷酸酶活性最佳在45℃下不搅拌。 TG-2分离物使用API​​ 50的最高肌醇六磷酸分解活性的表征和鉴定CH和的16S rRNA显示出与发酵乳杆菌的是TG-2had同源性。可以得出结论:从发酵传统粮食基和豆科植物系所产生的胞外植酸酶该LAB。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号