Bergan T, Vaksvik A K
Zentralbl Bakteriol Mikrobiol Hyg A Med Mikrobiol Infekt Parasitol. 1983 Apr;254(2):214-28.
Quantitative transformation of streptomycin resistance marker was carried out with strains of Acinetobacter calcoaceticus. Standard recipient strain was the competent BD4-Ss. Transformation proceeded in a liquid system with a concentration of 20 micrograms/ml of streptomycin resistant DNA (Sr-DNA) from BD4, 17 reference strains of Acinetobacter, and 42 recent clinical isolates of the acid forming variant (anitratus) and 12 of the non-acid forming variant (lwoffi) as donors of Sr-DNA. The exposure time was 20 min before interruption with DNase and quantitated plating. Among the strains examined were differentiated 16 biotypes as based on oxidative acid production from glucose and lactose, haemolysis, urease, gelatinase, and growth with citrate as the sole carbon source. Autologous transformation gave a transformation of 2.94 (+/- 0.66)% of the recipient cells (quantitated by colony forming units). Sr-DNA from 50 of 63 strains were able to transform BD4-Ss. The transformation ratio was 0.06-6.4% of autologous BD4 transformation. Two further recent clinical isolates were weakly transformation competent. Competence was only found in autologous transformation. The major portion (50/63) of the strains belong to the BD4 genotype of A. calcoaceticus, but the taxonomic position of the 13 non-donors in respect to BD4 could not be evaluated by transformation because of lack of a competent recipient. The strains transforming BD4 belonged to both the glucose acidifyers and the non-acidifyers without genetic distinction. The results are consistent with recognition of both as belonging to the same species, but with their recognition as species variants: A calcoaceticus var, anitratum and A. calcoaceticus var. lwoffi.
用醋酸钙不动杆菌菌株进行了链霉素抗性标记的定量转化。标准受体菌株是感受态BD4-Ss。转化在液体系统中进行,使用来自BD4、17株不动杆菌参考菌株以及42株近期临床分离的产酸变种(无硝亚种)和12株非产酸变种(鲁氏亚种)的浓度为20微克/毫升的链霉素抗性DNA(Sr-DNA)作为Sr-DNA供体。在加入DNA酶中断反应和定量铺板之前,暴露时间为20分钟。在所检测的菌株中,根据葡萄糖和乳糖的氧化产酸、溶血、脲酶、明胶酶以及以柠檬酸盐作为唯一碳源的生长情况,区分出了16种生物型。自体转化使受体细胞的转化率为2.94(±0.66)%(通过菌落形成单位定量)。63株菌株中的50株的Sr-DNA能够转化BD4-Ss。转化率为自体BD4转化的0.06 - 6.4%。另外两株近期临床分离株转化能力较弱。仅在自体转化中发现有感受态。大部分(50/63)菌株属于醋酸钙不动杆菌的BD4基因型,但由于缺乏合适的受体,13株非供体菌株相对于BD4的分类地位无法通过转化来评估。能够转化BD4的菌株既包括葡萄糖酸化菌,也包括非酸化菌,在遗传上没有区别。结果符合将两者都视为同一物种,但将它们视为物种变种的认识:醋酸钙不动杆菌无硝亚种和醋酸钙不动杆菌鲁氏亚种。