Suppr超能文献

[用含果胶物质的培养基分离软腐病菌的模型试验(作者译)]

[Model trials for isolation of soft rot bacteria by media containing pectic substances (author's transl)].

作者信息

Naumann K, Schmidt A

出版信息

Zentralbl Bakteriol Naturwiss. 1979;134(1):43-63.

PMID:473958
Abstract
  1. Under aerobic conditions bacterial soft rots are caused in the most cases by pectolytic Erwinia, Pseudomonas, and Bacillus spp. 2. Using 7 soft rotting strains several selective media were tested for their ability to sure a quick and exact isolation and differentiation of these pathogens. By bile salt-lactose-medium all Erwinia spp. under test could be isolated. For isolation of pectinolytic Pseudomonas strains the D4 medium of Kado and Heskett was suitable as the best one. 3. By the use of substrats containing pectic substances the results of isolation could be essentially improved: So, a sure differentiation of soft rotting bacteria and saprophytic organisms already upon the substrate and in addition, the isolation of pectinolytic Bacillus strains also became possible. The pectinolytic activity of the test strains on pectin-double layer-media was dependent upon the composition of the basal medium. 4. On the base of the results we obtained an isolation scheme is proposed, that allowed to indicate the pectolytic active bacilli (after heating to 80 degrees C for 10 min) on thioglycollate medium covered by a pectin layer, the Erwinia spp. on Stewart-Medium covered by pectin layer and the pectolytic pseudomonads on FPA-medium described by Sands, Hankin and Zucker (containing citrus pectin) to the equal time. 5. The trials also demonstrated, that the preparing of double layer-media instead of sodium polypectate mostly being recommended in literature lower estered pectic compounds can be used successfully.
摘要
  1. 在有氧条件下,细菌性软腐病大多由果胶分解型欧文氏菌属、假单胞菌属和芽孢杆菌属引起。2. 使用7种软腐病菌株测试了几种选择性培养基,以确定它们能否快速、准确地分离和鉴别这些病原体。通过胆盐乳糖培养基,可以分离出所有受试的欧文氏菌属菌株。对于果胶分解型假单胞菌菌株的分离,Kado和Heskett的D4培养基是最合适的。3. 通过使用含有果胶物质的底物,分离结果可得到显著改善:这样,在底物上就能可靠地区分软腐病菌和腐生生物,此外,还能分离出果胶分解型芽孢杆菌菌株。受试菌株在果胶双层培养基上的果胶分解活性取决于基础培养基的成分。4. 根据我们获得的结果,提出了一种分离方案,该方案能够在覆盖有果胶层的硫乙醇酸盐培养基上(在80℃加热10分钟后)鉴定出果胶分解活性芽孢杆菌,在覆盖有果胶层的Stewart培养基上鉴定出欧文氏菌属,在Sands、Hankin和Zucker描述的FPA培养基(含有柑橘果胶)上同时鉴定出果胶分解型假单胞菌。5. 试验还表明,制备双层培养基时,不必像文献中大多推荐的那样使用聚果胶酸钠,较低酯化度的果胶化合物也可成功使用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验