Xu Youqiang, Ma Yuyue, Yao Su, Jiang Zengyan, Pei Jiangsen, Cheng Chi
China Center of Industrial Culture Collection, China National Research Institute of Food and Fermentation Industries, Beijing, 100015, People's Republic of China.
Engineering Technology Research Center of Fumaric Acid Biotransformation in Shandong Province, Yantai, Shandong Province, 265709, People's Republic of China.
Food Environ Virol. 2016 Mar;8(1):18-26. doi: 10.1007/s12560-015-9218-0. Epub 2015 Oct 26.
Escherichia phage CICC 80001 was isolated from the bacteriophage contaminated medium of an Escherichia coli strain HY-05C (CICC 11022S) which could produce L-aspartic acid. The phage had a head diameter of 45-50 nm and a tail of about 10 nm. The one-step growth curve showed a latent period of 10 min and a rise period of about 20 min. The average burst size was about 198 phage particles per infected cell. Tests were conducted on the plaques, multiplicity of infection, and host range. The genome of CICC 80001 was sequenced with a length of 38,810 bp, and annotated. The key proteins leading to host-cell lysis were phylogenetically analyzed. One protein belonged to class II holin, and the other two belonged to the endopeptidase family and N-acetylmuramoyl-L-alanine amidase family, respectively. The genome showed the sequence identity of 82.7% with that of Enterobacteria phage T7, and carried ten unique open reading frames. The bacteriophage resistant E. coli strain designated CICC 11021S was breeding and its L-aspartase activity was 84.4% of that of CICC 11022S.
大肠杆菌噬菌体CICC 80001是从一株能产生L-天冬氨酸的大肠杆菌菌株HY-05C(CICC 11022S)的被噬菌体污染的培养基中分离得到的。该噬菌体头部直径为45-50nm,尾部约10nm。一步生长曲线显示潜伏期为10分钟,上升期约为20分钟。平均裂解量约为每个感染细胞产生198个噬菌体颗粒。对噬菌斑、感染复数和宿主范围进行了测试。对CICC 80001的基因组进行了测序,长度为38810bp,并进行了注释。对导致宿主细胞裂解的关键蛋白进行了系统发育分析。一种蛋白属于II类孔蛋白,另外两种蛋白分别属于内肽酶家族和N-乙酰胞壁酰-L-丙氨酸酰胺酶家族。该基因组与肠道杆菌噬菌体T7的序列同一性为82.7%,并携带10个独特的开放阅读框。选育了抗噬菌体的大肠杆菌菌株CICC 11021S,其L-天冬氨酸酶活性为CICC 11022S的84.4%。