Herren Christopher D, Peister Alexandra, Breton Timothy S, Hill Maggie S, Anderson Marcy S, Chang Adeline W, Klein Sydney B, Thornton Mackenzie M, Vars Stacy J, Wagner Kasey E, Wiebe Paige L, Williams Thomas G, Yanez Coraima P, Ackles Jasanta M, Artis Darius, Brazier Ryan J, Bryant Ronald J, Callwood Kerel O, Carter Isaiah H, DeBose Cameron L, Edwards Christian D, Ezemba Isaiah C, Joaquin Renshal R, Meghoo-Peddie Zakai M, Meghoo-Peddie Ziha G, Moore Ryan W, Smith Christopher E, Turner Adam J, Vorters Raymond L, Wider Jeffrey J, Krout Liesel L, Comis Mia S, Davick Madison J, Michaud Eli E, Shevenell Bailey E, Stanley Sarah E, Frank Chelsey I, Montgomery Jacob R, Blumer Lawrence S, Doty Jean A, Smith-Caldas Martha, Pope Welkin H, Cresawn Steven G, Russell Daniel A, Garlena Rebecca A, Jacobs-Sera Deborah, Hatfull Graham F
Division of Biology, Kansas State University, Manhattan, Kansas, USA.
Department of Biology, Morehouse College, Atlanta, Georgia, USA.
Genome Announc. 2017 Nov 16;5(46):e01233-17. doi: 10.1128/genomeA.01233-17.
Four subcluster L2 mycobacteriophages, Finemlucis, Miley16, Wilder, and Zakai, that infect mc155 were isolated. The four phages are closely related to each other and code for 12 to 14 tRNAs and 130 to 132 putative protein-coding genes, including tyrosine integrases, , immunity repressors, and excise genes involved in the establishment of lysogeny.
分离出了四种感染mc155的亚簇L2分枝杆菌噬菌体，即Finemlucis、Miley16、Wilder和Zakai。这四种噬菌体彼此密切相关，编码12至14个tRNA和130至132个推定的蛋白质编码基因，包括酪氨酸整合酶、免疫抑制因子以及参与溶原性建立的切除基因。
