Trautwetter A, Blanco C, Sicard A M
J Virol. 1987 May;61(5):1540-5. doi: 10.1128/JVI.61.5.1540-1545.1987.
Bacteriophage CL31 was isolated on a Corynebacterium lilium strain. Out of 30 strains tested, only CL31 was able to form plaques on Corynebacterium glutamicum ATCC 13287, Brevibacterium lactofermentum ATCC 21086, and Arthrobacter sp. strain SI55, but at a very low frequency. This phage belongs to group B of Bradley's classification (D. E. Bradley, Bacteriol. Rev. 31:230-314; 1967). Its head is 53 nm in diameter, and its tail is 396 nm in length. The phage capsid contains three major proteins, of 12.5, 29.0, and 37.0 kilodaltons, and five minor ones (23.9, 26.0, 27.0, 40.0, and 55.4 kilodaltons). CL31 DNA is a linear molecule of 48 kilobases with cohesive ends. Restriction mapping was performed for endonucleases BglII, EcoRI, SalI, and KpnI. The expression of CL31 genes in Escherichia coli was studied by the maxicell technique; 12 different proteins were detected.
噬菌体CL31是从一株百合棒状杆菌中分离出来的。在测试的30株菌株中,只有CL31能够在谷氨酸棒杆菌ATCC 13287、乳酸发酵短杆菌ATCC 21086和节杆菌属菌株SI55上形成噬菌斑,但频率很低。该噬菌体属于布拉德利分类法中的B组(D. E. 布拉德利,《细菌学评论》31:230 - 314;1967年)。它的头部直径为53纳米,尾部长度为396纳米。噬菌体衣壳包含三种主要蛋白质,分子量分别为12.5、29.0和37.0千道尔顿,以及五种次要蛋白质(23.9、26.0、27.0、40.0和55.4千道尔顿)。CL31 DNA是一个具有粘性末端的48千碱基线性分子。对核酸内切酶BglII、EcoRI、SalI和KpnI进行了限制性图谱分析。通过大细胞技术研究了CL31基因在大肠杆菌中的表达;检测到了12种不同的蛋白质。