Sreenivasan P K, Meyer D H, Fives-Taylor P M
Laboratory of Molecular Infectious Diseases, Rockefeller University, New York.
Oral Microbiol Immunol. 1993 Dec;8(6):361-9. doi: 10.1111/j.1399-302x.1993.tb00612.x.
The metabolic requirements for the routine growth of Actinobacillus actinomycetemcomitans were investigated by the addition of nutrients to conventional bacteriological and tissue culture media. Commonly used tissue culture media required fetal bovine serum as an additive to sustain bacterial growth rates comparable to those obtained with bacteriological media. The addition of increasing concentrations of yeast extract to bacteriological medium increased the growth rate of several A. actinomycetemcomitans strains. In an attempt to identify the components of yeast extract that enhanced the growth of A. actinomycetemcomitans, a number of vitamins, essential and non-essential amino acids were tested for their role in promoting growth. The addition of L-cystine resulted in bacterial growth rates comparable to those with yeast extract. Thiamine increased the growth of several A. actinomycetemcomitans strains but did not result in growth rates comparable to those with yeast extract. The addition of physiological concentrations of steroid hormones to bacteriological medium enhanced the growth of A. actinomycetemcomitans. Additional iron compounds and fat-soluble vitamins had no influence on A. actinomycetemcomitans growth. However, the requirement of iron for bacterial growth remains unclear. The optimal pH range for growth of A. actinomycetemcomitans was between pH 7.0-8.0 in a medium containing 0.5-1% NaCl. Several interesting observations on the viability of A. actinomycetemcomitans were made. A rapid reduction of A. actinomycetemcomitans viability occurred following suspension in distilled water. The presence of the detergent Triton X-100 at concentrations above 2% (v/v) also decreased the viability of A. actinomycetemcomitans within 10 min.
通过向传统细菌学培养基和组织培养基中添加营养物质,研究了伴放线放线杆菌常规生长的代谢需求。常用的组织培养基需要添加胎牛血清才能维持与细菌学培养基相当的细菌生长速率。向细菌学培养基中添加浓度不断增加的酵母提取物可提高几种伴放线放线杆菌菌株的生长速率。为了确定酵母提取物中促进伴放线放线杆菌生长的成分,测试了多种维生素、必需氨基酸和非必需氨基酸在促进生长方面的作用。添加L-胱氨酸可使细菌生长速率与添加酵母提取物时相当。硫胺素可促进几种伴放线放线杆菌菌株的生长,但生长速率无法与添加酵母提取物时相比。向细菌学培养基中添加生理浓度的甾体激素可促进伴放线放线杆菌的生长。额外添加铁化合物和脂溶性维生素对伴放线放线杆菌的生长没有影响。然而,细菌生长对铁的需求仍不明确。在含有0.5-1%氯化钠的培养基中,伴放线放线杆菌生长的最佳pH范围为7.0-8.0。关于伴放线放线杆菌的生存能力有一些有趣的观察结果。将伴放线放线杆菌悬浮于蒸馏水中后,其生存能力迅速下降。浓度高于2%(v/v)的去污剂 Triton X-100在10分钟内也会降低伴放线放线杆菌的生存能力。