본 연구에서는 2014년 국내에서 식중독 원인식품인 김밥으로부터 분리된 Salmonella Enteritidis의 유전체 분석을 수행하였다. Salmonella Enteritidis MFDS1004839는 한 개의 chromosome (4,679,649 bp)과 plasmid (96,994 bp)로 구성되어있고, 각각의 G + C contents는 52.2%와 49.3%로 확인되었다. chromosome와 plasmid DNA에 예측된 유전자의 총 수는 4,482개의 단백질 코딩유전자와 84개 tRNA, 그리고 22개의 rRNA였다.
본 연구에서는 2014년 국내에서 식중독 원인식품인 김밥으로부터 분리된 Salmonella Enteritidis의 유전체 분석을 수행하였다. Salmonella Enteritidis MFDS1004839는 한 개의 chromosome (4,679,649 bp)과 plasmid (96,994 bp)로 구성되어있고, 각각의 G + C contents는 52.2%와 49.3%로 확인되었다. chromosome와 plasmid DNA에 예측된 유전자의 총 수는 4,482개의 단백질 코딩유전자와 84개 tRNA, 그리고 22개의 rRNA였다.
Salmonella enterica subsp. enterica is a foodborne pathogen that has been detected throughout the world. Here, we present the complete genome sequence of Salmonella Enteritidis isolated from a commercial kimbap that caused foodborne illness in the Republic of Korea in 2014. Complete genome sequence ...
Salmonella enterica subsp. enterica is a foodborne pathogen that has been detected throughout the world. Here, we present the complete genome sequence of Salmonella Enteritidis isolated from a commercial kimbap that caused foodborne illness in the Republic of Korea in 2014. Complete genome sequence analysis of Salmonella Enteritidis MFDS1004839 revealed a 4,679,649 bp chromosome and a 96,994 bp plasmid, with G + C contents of 52.2% and 49.3%, respectively. The chromosome and plasmid genome included 4,482 predicted protein-coding sequences, 84 tRNAs and 22 rRNAs genes.
Salmonella enterica subsp. enterica is a foodborne pathogen that has been detected throughout the world. Here, we present the complete genome sequence of Salmonella Enteritidis isolated from a commercial kimbap that caused foodborne illness in the Republic of Korea in 2014. Complete genome sequence analysis of Salmonella Enteritidis MFDS1004839 revealed a 4,679,649 bp chromosome and a 96,994 bp plasmid, with G + C contents of 52.2% and 49.3%, respectively. The chromosome and plasmid genome included 4,482 predicted protein-coding sequences, 84 tRNAs and 22 rRNAs genes.
* AI 자동 식별 결과로 적합하지 않은 문장이 있을 수 있으니, 이용에 유의하시기 바랍니다.
문제 정의
본 연구에서는 2014년 국내에서 식중독 원인식품인 김밥으로부터 분리된 Salmonella Enteritidis의 유전체 분석을 수행하였다. Salmonella Enteritidis MFDS1004839는 한 개의 chromosome (4,679,649 bp)과 plasmid (96,994 bp)로
대상 데이터
enterica Serovar Enteritidis (also known as Salmonella Enteritidis) MFDS1004839 was isolated from a commercial kimbap that caused foodborne disease in the Republic of Korea in 2014. The isolate has been deposited at Korean Culture Collection for Foodborne Pathogens under the strain number MFDS1004839. Here, we report the complete genome sequence of Salmonella Enteritidis MFDS1004839.
3%로 확인되었다. chromosome와 plasmid DNA에 예측된 유전자의 총 수는 4,482개의 단백질 코딩유전자와 84개 tRNA, 그리고 22개의 rRNA였다.
성능/효과
3%, respectively. As a result of gene prediction, this strain was found to possess 4,359 CDSs, 84 tRNAs and 22 rRNAs in the chromosome and 123 CDSs in pSE1004839. The serovar of Salmonella Enteritidis MFDS1004839 was predicted to be 9:g,m:-(O antigen: 9, H antigen phase1: g,m, H antigen phase2: not detected) Enteritidis using SeqSero software (Zhang et al.
후)원인 식품인">원인식품인 김밥으로부터 분리된 Salmonella Enteritidis의 유전체 분석을 수행하였다. Salmonella Enteritidis MFDS1004839는 한 개의 chromosome (4,679,649 bp)과 plasmid (96,994 bp)로 구성되어 있고, 각각의 G + C contents는 52.2%와 49.3%로 확인되었다. chromosome와 plasmid DNA에 예측된 유전자의
The complete genome sequence of Salmonella Enteritidis MFDS1004839 consisted of a 4,679,649 bp chromosome and a circular 96,994 bp plasmid (pSE1004839), with G + C contents of 52.2% and 49.3%, respectively. As a result of gene prediction, this strain was found to possess 4,359 CDSs, 84 tRNAs and 22 rRNAs in the chromosome and 123 CDSs in pSE1004839.
참고문헌 (13)
Bairoch, A. and Apweiler, R. 2000. The SWISS-PROT protein sequence database and its supplement TrEMBL in 2000. Nucleic Acids Res. 28, 45-48.
Das, A., Hari, S.S., Shalini, U., Ganeshkumar, A., and Karthikeyan, M. 2012. Molecular screening of virulence genes from Salmonella enterica isolated from commercial food stuffs. Biosci. Biotechnol. Res. Asia 9, 363-369.
Huerta-Cepas, J., Szklarczyk, D., Forslund, K., Cook, H., Heller, D., Walter, M.C., Rattei, T., Mende, D.R., Sunagawa, S., Kuhn, M., et al. 2015. eggNOG 4.5: a hierarchical orthology framework with improved functional annotations for eukaryotic, prokaryotic and viral sequences. Nucleic Acids Res. 44, D286-D293.
Hyatt, D., Chen, G.L., LoCascio, P.F., Land, M.L., Larimer, F.W., and Hauser, L.J. 2010. Prodigal: prokaryotic gene recognition and translation initiation site identification. BMC Bioinformatics 11, 119.
Kim, S. 2010. Salmonella serovars from foodborne and waterborne diseases in Korea, 1998-2007: total isolates decreasing versus rare serovars emerging. J. Korean Med. Sci. 25, 1693-1699.
Lee, W.C., Lee, M.J., Kim, J.S., and Park, S.Y. 2001. Foodborne illness outbreaks in Korea and Japan studied retrospectively. J. Food Prot. 64, 899-902.
Lowe, T.M. and Eddy, S.R. 1997. tRNAscan-SE: a program for improved detection of transfer RNA genes in genomic sequence. Nucleic Acids Res. 25, 955-964.
Overbeek, R., Olson, R., Pusch, G.D., Olsen, G.J., Davis, J.J., Disz, T., Edwards, R.A., Gerdes, S., Parrello, B., Shukla, M., et al. 2014. The SEED and the rapid annotation of microbial genomes using subsystems technology (RAST). Nucleic Acids Res. 42, D206-D214.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.