Sequencing, Characterization, and Gene Expression Analysis of the Histidine Decarboxylase Gene Cluster of Morganella morganii

被引:19
作者
Ferrario, Chiara [1 ]
Borgo, Francesca [1 ]
de las Rivas, Blanca [2 ]
Munoz, Rosario [2 ]
Ricci, Giovanni [1 ]
Fortina, Maria Grazia [1 ]
机构
[1] Univ Milan, Dept Food Environm & Nutr Sci DeFENS, I-20133 Milan, Italy
[2] CSIC, ICTAN, Lab Biotecnol Bacteriana, Madrid, Spain
关键词
LIGATION-INDEPENDENT CLONING; HISTAMINE-PRODUCING BACTERIA; TRANSFER-RNA SYNTHETASE; BIOGENIC-AMINES; QUANTITATIVE PCR; FISH; BIOSYNTHESIS; VECTORS;
D O I
10.1007/s00284-013-0490-7
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The histidine decarboxylase gene cluster of Morganella morganii DSM30146(T) was sequenced, and four open reading frames, named hdcT1, hdc, hdcT2, and hisRS were identified. Two putative histidine/histamine antiporters (hdcT1 and hdcT2) were located upstream and downstream the hdc gene, codifying a pyridoxal-P dependent histidine decarboxylase, and followed by hisRS gene encoding a histidyl-tRNA synthetase. This organization was comparable with the gene cluster of other known Gram negative bacteria, particularly with that of Klebsiella oxytoca. Recombinant Escherichia coli strains harboring plasmids carrying the M. morganii hdc gene were shown to overproduce histidine decarboxylase, after IPTG induction at 37 A degrees C for 4 h. Quantitative RT-PCR experiments revealed the hdc and hisRS genes were highly induced under acidic and histidine-rich conditions. This work represents the first description and identification of the hdc-related genes in M. morganii. Results support the hypothesis that the histidine decarboxylation reaction in this prolific histamine producing species may play a role in acid survival. The knowledge of the role and the regulation of genes involved in histidine decarboxylation should improve the design of rational strategies to avoid toxic histamine production in foods.
引用
收藏
页码:404 / 411
页数:8
相关论文
共 32 条
[1]   DNA signature-based approaches for bacterial detection and identification [J].
Albuquerque, Pedro ;
Mendes, Marta V. ;
Santos, Catarina L. ;
Moradas-Ferreira, Pedro ;
Tavares, Fernando .
SCIENCE OF THE TOTAL ENVIRONMENT, 2009, 407 (12) :3641-3651
[2]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[3]  
[Anonymous], 1989, Molecular Cloning: A Laboratory
[4]   The pURI family of expression vectors: A versatile set of ligation independent cloning plasmids for producing recombinant His-fusion proteins [J].
Antonio Curiel, Jose ;
de las Rivas, Blanca ;
Miguel Mancheno, Jose ;
Munoz, Rosario .
PROTEIN EXPRESSION AND PURIFICATION, 2011, 76 (01) :44-53
[5]   CRYSTAL-STRUCTURE OF HISTIDYL-TRANSFER-RNA SYNTHETASE FROM ESCHERICHIA-COLI COMPLEXED WITH HISTIDYL-ADENYLATE [J].
ARNEZ, JG ;
HARRIS, DC ;
MITSCHLER, A ;
REES, B ;
FRANCKLYN, CS ;
MORAS, D .
EMBO JOURNAL, 1995, 14 (17) :4143-4155
[6]   Detection of Gram-Negative Histamine-Producing Bacteria in Fish: A Comparative Study [J].
Bjornsdottir, Kristin ;
Bolton, Gregory E. ;
McClellan-Green, Patricia D. ;
Jaykus, Lee-Ann ;
Green, David P. .
JOURNAL OF FOOD PROTECTION, 2009, 72 (09) :1987-1991
[7]  
Davies H., 2010, Food Control, V21, P1601
[8]   Expression vectors for enzyme restriction- and ligation-independent cloning for producing recombinant his-fusion proteins [J].
de las Rivas, Blanca ;
Curiel, Jose Antonio ;
Mancheno, Jose Miguel ;
Munoz, Rosario .
BIOTECHNOLOGY PROGRESS, 2007, 23 (03) :680-686
[9]  
Eitenmiller R. R., 1984, SEAFOOD TOXINS, P431
[10]   Species-specific DNA probe and development of a quantitative PCR assay for the detection of Morganella morganii [J].
Ferrario, C. ;
Ricci, G. ;
Borgo, F. ;
Fortina, M. G. .
LETTERS IN APPLIED MICROBIOLOGY, 2012, 54 (04) :292-298