Jeyaram K, Mohendro Singh W, Premarani T, Devi A Ranjita, Chanu K Selina, Talukdar N C, Singh M Rohinikumar
Microbial Resources Division, Institute of Bioresources and Sustainable Development, Takyelpat Institutional Area, Imphal-795001, Manipur, India.
Int J Food Microbiol. 2008 Mar 20;122(3):259-68. doi: 10.1016/j.ijfoodmicro.2007.12.026. Epub 2008 Jan 12.
The dominant microorganisms in 'Hawaijar', a traditional non-salted fermented soybean (Glycine max (L.)) food of Manipur, India, were isolated and identified by molecular techniques. Bacillus spp. were the predominant microorganisms in 'Hawaijar'. A total of 274 isolates were obtained from forty-one 'Hawaijar' samples collected from household preparations and markets of valley districts of Manipur. Phenotypic grouping followed by Amplified Ribosomal DNA Restriction Digestion Analysis (ARDRA), PCR amplification of 16S-23S rDNA region, RFLP by Hae III and Hind III double digest (by comparing MTCC type strains) and sequencing of 9-1514 region of 16S rDNA resulted in three major phylogenic groups. Bacillus subtilis group comprising B. subtilis and B. licheniformis representing 112 isolates, B. cereus group representing of 128 isolates and Staphylococcus spp. group comprising S. aureus and S. sciuri representing 23 isolates. A few bacterial isolates belongs to Alkaligenes spp. and Providencia rettgeri were also found. Genetic diversity of B. subtilis phylogenic group was investigated by RAPD-PCR. Eighty-two strains of B. subtilis phylogenic group were identified using RAPD-PCR using OPA-18 and OPA-20 primers. These strains will be investigated for potential starter culture selection.
通过分子技术对印度曼尼普尔邦一种传统的未加盐发酵大豆(大豆)食品“Hawaijar”中的优势微生物进行了分离和鉴定。芽孢杆菌属是“Hawaijar”中的主要微生物。从曼尼普尔邦山谷地区家庭制作和市场收集的41个“Hawaijar”样品中总共获得了274株分离株。通过表型分组,然后进行核糖体DNA限制性内切酶分析(ARDRA)、16S - 23S rDNA区域的PCR扩增、Hae III和Hind III双酶切的RFLP分析(通过与MTCC模式菌株比较)以及16S rDNA的9 - 1514区域测序,得到了三个主要的系统发育组。枯草芽孢杆菌组包括枯草芽孢杆菌和地衣芽孢杆菌,共112株分离株;蜡样芽孢杆菌组有128株分离株;葡萄球菌属组包括金黄色葡萄球菌和松鼠葡萄球菌,共23株分离株。还发现了一些属于产碱杆菌属和雷氏普罗威登斯菌的细菌分离株。通过RAPD - PCR研究了枯草芽孢杆菌系统发育组的遗传多样性。使用OPA - 18和OPA - 20引物通过RAPD - PCR鉴定了82株枯草芽孢杆菌系统发育组的菌株。这些菌株将被研究用于潜在的发酵剂筛选。