Gross culture system for cyanobacteria & its application for medication
蓝藻粗培养系统
基本信息
- 批准号:03557024
- 负责人:
- 金额:$ 10.94万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Developmental Scientific Research (B)
- 财政年份:1991
- 资助国家:日本
- 起止时间:1991 至 1993
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
A gross culture system for microcystis (cyanobactera) has been developed. When the cells of Microcystis aeruginosa K-139 strain were inoculated (10% v/v) into the system with 10 litters of CB medium (pH 10.0) and were cultured at 28C。 under the conditions of airing (filter-passed air, 9 liters/min) and lighting (4 directions, cool white light, 10, 000 lux). The pH of medium was maintained between 9 and 10, by being adjusted with 1 N HCl solution during the culture period. The cell-growth reached the maximum at day 7, and the yield of cells was 4.56 g. It was 2.5 times greater than that obtained from a stationary culture. The yield of microcystin extracted from the cell-mass was 27.493 mg, and it was 3 times more than that of the statinary culture.Monoclonal antibodies against microcystin-LR were prepared from hybridoma cell lines. All the antibodies were reacted with not only microcystin-LR but also other microcystins tested. Microcystin-shock in mice could hardly be protected by a previous administration of these antibodies. The microcystin-shock was relieved to some extent when interleukin (IL)-10 was injected 30 min in advance. The serum-level of IL-6 induced by microcystin was lowered by a previous injection of IL-10.The cell-extract of Microcystis aeruginosa K-18 strain contained anti-bacterial activity against various kinds of gram-positive and negative bacteria. The active substance was purified. However, it was found to be gamma-linolenic acid.
建立了微囊藻(蓝藻)的整体培养系统。将铜绿微囊藻K-139菌株的细胞接种到含有10升CB(pH 10.0)的培养液中,在28℃下培养。在通风(过滤器通过的空气,9升/分钟)和照明(4个方向,冷白光,10,000勒克斯)的条件下。在培养过程中,用1N的HCl溶液调节培养基的pH值,使其保持在9~10之间。细胞生长在第7天达到最大值,细胞产量为4.56g,是静止培养的2.5倍。从菌体中提取的微囊藻毒素产量为27.493 mg,是原发酵液的3倍。所有抗体不仅与微囊藻毒素-LR反应,还与其他微囊藻毒素反应。小鼠的微囊藻毒素休克几乎不能通过以前注射这些抗体来保护。提前30min注射IL-10可在一定程度上缓解微囊藻毒素休克。预先注射IL-10可降低微囊藻毒素诱导的血清IL-6水平。铜绿微囊藻K-18菌株细胞提取物对各种革兰氏阳性菌和阴性菌均有抗菌活性。对活性物质进行了纯化。然而,它被发现是伽马亚麻酸。
项目成果
期刊论文数量(11)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Shirai, M., et al.: "Toxicity and toxins of natural blooms and isolated strains of Microcystis spp. (cyanobacteria) and improved procedure for purification of cultures" Appl.Environ.Microbiol.57. 1241-1245 (1991)
Shirai, M. 等人:“天然花朵和微囊藻属(蓝藻)分离菌株的毒性和毒素以及培养物纯化的改进程序”Appl.Environ.Microbiol.57。
- DOI:
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- 影响因子:0
- 作者:
- 通讯作者:
Shirai,M.et al.: "Release of microcystin from Microcystis cells." Appl.Environ.Microbiol.
Shirai,M.et al.:“从微囊藻细胞中释放微囊藻毒素。”
- DOI:
- 发表时间:
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- 影响因子:0
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- 通讯作者:
白井 誠 他: "Microcystis シアノバクテリアの毒性" 日本細菌学雑誌. 48. 511-522 (1993)
Makoto Shirai 等人:“蓝藻微囊藻的毒性”,日本细菌学杂志 48. 511-522 (1993)。
- DOI:
- 发表时间:
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- 影响因子:0
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- 通讯作者:
S.Saito 他: "Cross-reactivity and neutraliging ability of monoclonal antibodies against microcystins" Microbiology and Immunology. 38(印刷中). (1994)
S. Saito 等人:“针对微囊藻毒素的单克隆抗体的交叉反应性和中和能力”微生物学和免疫学 38(出版中)。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Nakano,Y.et al.: "Neutralization of microcystin shock in mice by tumor necrosis factor alpha antiserum." Appl.Environ.Microbiol.57. 327-330 (1991)
Nakano,Y.et al.:“肿瘤坏死因子 α 抗血清对小鼠微囊藻毒素休克的中和作用。”
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- 影响因子:0
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NAKANO Masayasu其他文献
NAKANO Masayasu的其他文献
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{{ truncateString('NAKANO Masayasu', 18)}}的其他基金
Analysis of specific protein phosphorylation after infection with bacteria
细菌感染后特异性蛋白质磷酸化分析
- 批准号:
05454194 - 财政年份:1993
- 资助金额:
$ 10.94万 - 项目类别:
Grant-in-Aid for General Scientific Research (B)
Molecular mechanisms of bacterial toxins on host cells
细菌毒素对宿主细胞的分子机制
- 批准号:
04304032 - 财政年份:1992
- 资助金额:
$ 10.94万 - 项目类别:
Grant-in-Aid for Co-operative Research (A)
Molecular biology on murine macrophage activated by bacterial infection or bacterial components
细菌感染或细菌成分激活小鼠巨噬细胞的分子生物学
- 批准号:
03454184 - 财政年份:1991
- 资助金额:
$ 10.94万 - 项目类别:
Grant-in-Aid for General Scientific Research (B)
Production of Cytokines After Stimulation of Bacterial Components And Protective Role of the Cytokines to Bacterial Infection
细菌成分刺激后细胞因子的产生及其对细菌感染的保护作用
- 批准号:
01480180 - 财政年份:1989
- 资助金额:
$ 10.94万 - 项目类别:
Grant-in-Aid for General Scientific Research (B)
Signal Transmittance on Interferon-gamma-Treated Murine Immunocompetent Cells
干扰素γ处理的鼠免疫活性细胞的信号透射率
- 批准号:
63044127 - 财政年份:1988
- 资助金额:
$ 10.94万 - 项目类别:
Grant-in-Aid for Overseas Scientific Survey.
Production and role of Macrophage activating factor (IFN-gamma) by bacterial lipopolysaccharide and other bacterial products
细菌脂多糖和其他细菌产物产生巨噬细胞激活因子(IFN-γ)及其作用
- 批准号:
61480149 - 财政年份:1986
- 资助金额:
$ 10.94万 - 项目类别:
Grant-in-Aid for General Scientific Research (B)
相似国自然基金
微囊藻毒素microcystin-LR通过调节MAPK信号通路影响斑马鱼卵母细胞减数分裂的机制研究
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