著者
熊谷 浩一 田中 尚人 佐藤 英一 岡田 早苗 Kumagai Koichi Naoto Tanaka Eiichi Satoh Sanae Okada 東京農業大学大学院農学研究科農芸化学専攻 東京農業大学応用生物科学部菌株保存室 東京農業大学応用生物科学部生物応用化学科 東京農業大学応用生物科学部生物応用化学科 Department of Agricultural Chemistry Tokyo University of Agriculture NRIC Tokyo University of Agriculture Department of Applied Biology and Chemistry Tokyo University of Agriculture Department of Applied Biology and Chemistry Tokyo University of Agriculture
出版者
東京農業大学
雑誌
東京農業大学農学集報 (ISSN:03759202)
巻号頁・発行日
vol.59, no.4, pp.274-282,

長崎県対馬市は南北に長い島であり,対馬のそれぞれの農家ではサツマイモを原料とした固有の伝統保存食品である『せんだんご』を小規模に製造している。 せんだんごは,水で戻し,捏ねた生地を麺状に加工して茹であげ『ろくべえ麺』として食される。 ろくべえは,原料であるサツマイモ単体では生じ得ない食感を有していることから,せんだんごの製造工程に着目した。 せんだんごの製造には,"芋を腐らせる(発酵させる)"工程,それを丸めて数ヶ月に及ぶ軒下での"寒晒し"の工程があることから,島内各地域の「せんだんご製造農家」を訪問し,製造方法の調査を行った。 その結果,これら両工程にはカビなどの微生物が繁殖しており,黒色カビが繁殖した場合は味が悪くなるという理由からその部位が破棄され,白色や青色カビが繁殖した部位の製造が続行される。 このことから微生物の働きがあってせんだんごとなり,さらにろくべえ麺特有の食感が与えられると推察した。 さらに,せんだんご製造に重要な働きをすると考えられる微生物を特定するにあたり,数年にわたり島内の調査を重ねた結果,基本的にはせんだんご製造工程には3段階の発酵工程(発酵1(浸漬),発酵2(棚板に広げて発酵),発酵3(ソフトボール大の塊で発酵))と洗浄・成型工程の2工程4区分に分けられることが確認された。Sendango is an indigenous preserved food derived from sweet potato that is traditionally made in Tsushima, Japan located between the Korean Peninsula and Kyushu. The local people process a noodle called Rokube from Sendango and eat it with soup, fish or chicken. Rokube has a unique texture similar to konyaku, and unlike that of cooked sweet potato. There are two or three fermentation processes involved in Sendango production; therefore, we inferred that the unique texture of Rokube may result from the fermentation process. Sendango is manufactured in several farmhouses on the island ; however, the manufacturing process varies among districts. We investigated each local Sendango manufacturing process and determined the microorganisms involved in fermentation. The investigation of Sendango manufacturing procedures was carried out in three towns, Toyotama, Izuhara, and Mitsushima, by interviews and observations between December and February each year from 2008 to 2011. The processes consist of three main fermentations. In Fermentation-1 (F1), sliced or smashed sweet potatoes were soaked in cold water for 7-10 days. Gas production and film formation were observed during F1. In Fermentation-2 (F2), the soaked sweet potato pieces were piled to a thickness of 5-20cm for 20-30 days. Intense propagation of filamentous fungi was observed during F2. In fermentation-3 (F3), softball-sized lumps were formed on the sticky sweet potato by fungi. The sweet potatoes were left outside for approximately 1 month. The lumps gradually hardened by drying. Many fungal mycelia were observed on the surface of potatoes and inside the lumps during F3. The three aforementioned fermentation processes were used for Sendango production in two towns (Toyotama and Izuhara). In Izuhara, smashed sweet potatoes were placed in sandbags knit with plastic strings, and the bags were soaked in the flowing river water. The sandbags collected from the river water were left on the river bank for 20 days. F2 was carried out in sandbags. In Mitsushima, Sendango production consisted of two fermentation processes, F1 and F3. The fermentation process occurs over a long time period. The propagation of filamentous fungi was particularly intense during F2 and F3. It is thought that filamentous fungi are indispensable for Sendango production. We characterized the microorganisms participating in Sendango production based on this investigation.
著者
Hassadin BOONSRIROJ Daria Llenaresas MANALO Kazunori KIMITSUKI Taichi SIHMATSU Nozomi SHIWA Harumi SHINOZAKI Yurika TAKAHASHI Naoto TANAKA Satoshi INOUE Chun-Ho PARK
出版者
公益社団法人 日本獣医学会
雑誌
Journal of Veterinary Medical Science (ISSN:09167250)
巻号頁・発行日
pp.15-0308, (Released:2015-08-14)
被引用文献数
3 13

Rabies is a zoonotic disease caused by the rabies virus. While the salivary glands are important as exit and propagation sites for the rabies virus, the mechanisms of rabies excretion remain unclear. Here, we investigated the histopathology of the salivary glands of rabid dogs and analyzed the mechanism of excretion into the oral cavity. Mandibular and parotid glands of 22 rabid dogs and three control dogs were used. Mild to moderate non-suppurative sialadenitis was observed in the mandibular glands of 19 of the 22 dogs, characterized by loss of acinar epithelium and infiltration by lymphoplasmacytic cells. Viral antigens were detected in the mucous acinar epithelium, ganglion neurons and myoepithelium. Acinar epithelium and lymphocytes were positive for anti-caspase-3 antibodies and TUNEL staining. In contrast, no notable findings were observed in the ductal epithelial cells and serous demilune. In the parotid gland, the acinar cells, myoepithelium and ductal epithelium all tested negative. These findings confirmed the path through which the rabies virus descends along the facial nerve after proliferation in the brain to reach the ganglion neurons of the mandibular gland, subsequently traveling to the acinar epithelium via the salivary gland myoepithelium. Furthermore, the observation that nerve endings passing through the myoepithelium were absent from the ductal system suggested that viral proliferation and cytotoxicity could not occur there, ensuring that secretions containing the virus are efficiently excreted into the oral cavity.
著者
Shunta Kihara Kosuke Yamamoto Atsushi Hisatomi Yuh Shiwa Chia-Cheng Chu Kanako Takada Michel Ouyabe Babil Pachakkil Hidehiko Kikuno Naoto Tanaka Hironobu Shiwachi
出版者
Japanese Society of Microbial Ecology / Japanese Society of Soil Microbiology / Taiwan Society of Microbial Ecology / Japanese Society of Plant Microbe Interactions / Japanese Society for Extremophiles
雑誌
Microbes and Environments (ISSN:13426311)
巻号頁・発行日
vol.37, no.2, pp.ME21062, 2022 (Released:2022-05-03)
参考文献数
53
被引用文献数
3

The bacterial community of water yam (Dioscorea alata L.) cv. A-19 is vital because it may promote plant growth without the need for fertilization. However, the influence of fertilization practices on the composition and proportion of the bacterial community of water yam cv. A-19 has not yet been extensively examined. Therefore, we herein investigated the diversity and composition of the bacterial community of water yam cv. A-19 cultivated with and without chemical fertilization using amplicon community profiling based on 16S rRNA gene sequences. No significant difference was detected in the growth of plants cultivated with or without chemical fertilization. Alpha diversity indices were significantly dependent on each compartment, and a decrease was observed in indices from the belowground (rhizosphere and root) to aboveground compartments (stem and leaf). The bacterial composition of each compartment was clustered into three groups: bulk soil, rhizosphere and root, and stem and leaf. Chemical fertilization did not significantly influence the diversity or composition of the water yam cv. A-19 bacterial community. It remained robust in plants cultivated with chemical fertilization. The amplicon community profiling of bacterial communities also revealed the dominance of two bacterial clades, the Allorhizobium-Neorhizobium-Pararhizobium-Rhizobium clade and Burkholderia-Caballeronia-Paraburkholderia clade, with and without chemical fertilization. This is the first study to characterize the bacterial community of water yam cv. A-19 cultivated with and without chemical fertilization.
著者
Masahiro HATTORI Glaezel Angelique TORRES Naoto TANAKA Sanae OKADA Akihito ENDO Junichi NAKAGAWA
出版者
BMFH出版会
雑誌
Bioscience of Microbiota, Food and Health (ISSN:21863342)
巻号頁・発行日
vol.36, no.2, pp.65-72, 2017 (Released:2017-04-19)
参考文献数
23
被引用文献数
4

Penicillin-binding proteins (PBPs) are responsible for peptidoglycan synthesis. By using biotinylated ampicillin, we detected PBPs of Lactobacillus paracasei strains. Ten PBPs were identified, 7 of which had apparent molecular sizes similar to those of Escherichia coli. In the presence of cholate, strain NRIC 0625 showed an elongated shape, and its putative PBP3 showed cholate-sensitive penicillin-binding activity. Furthermore, this strain was highly sensitive to cefalexin, which is known to inhibit cell division by inactivating PBP3. These results suggest that the septum synthetase PBP3 of lactic acid bacteria can be one of the targets of intestinal bile acid.