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寻找自溶素的功能。lytA基因缺失的肺炎球菌突变体的特性研究。

Searching for autolysin functions. Characterization of a pneumococcal mutant deleted in the lytA gene.

作者信息

Sanchez-Puelles J M, Ronda C, Garcia J L, Garcia P, Lopez R, Garcia E

出版信息

Eur J Biochem. 1986 Jul 15;158(2):289-93. doi: 10.1111/j.1432-1033.1986.tb09749.x.

Abstract

The first mutant of Streptococcus pneumoniae showing a complete deletion in the lytA gene coding for the N-acetylmuramyl-L-alanine amidase has been isolated and characterized. This amidase was previously the only autolysin detected in this species. This mutant shows a normal growth rate and can be transformed using either chromosomal or plasmid DNA. The most remarkable biological consequences of the absence of the amidase are the formation of small chains (six to eight cells) and the absence of lysis in the stationary phase of growth. In addition, this mutant exhibits a tolerant response against the beta-lactam antibiotics.

摘要

已分离并鉴定出肺炎链球菌的首个突变体,该突变体在编码N - 乙酰胞壁酰 - L - 丙氨酸酰胺酶的lytA基因中存在完全缺失。这种酰胺酶以前是该物种中唯一检测到的自溶素。该突变体显示出正常的生长速率,并且可以使用染色体DNA或质粒DNA进行转化。酰胺酶缺失最显著的生物学后果是形成小链(六到八个细胞)以及在生长稳定期不发生裂解。此外,该突变体对β - 内酰胺类抗生素表现出耐受反应。

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