A physical map of the syringomycin and syringopeptin gene clusters localized to an approximately 145-kb DNA region of Pseudomonas syringae pv. syringae strain B301D

被引:33
作者
Scholz-Schroeder, BK
Soule, JD
Lu, SE
Grgurina, I
Gross, DC [1 ]
机构
[1] Texas A&M Univ, Dept Plant Pathol & Microbiol, College Stn, TX 77843 USA
[2] Washington State Univ, Dept Plant Pathol, Pullman, WA 99164 USA
[3] Univ Roma La Sapienza, Dipartimento Sci Biochim A Rossi Fanelli, Rome, Italy
关键词
lipopeptide toxin; necrosis-inducing phytotoxin; virulence determinant;
D O I
10.1094/MPMI.2001.14.12.1426
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Genetic and phenotypic mapping of an approximately 145-kb DraI fragment of Pseudomonas syringae pv. syringae strain B301D determined that the syringomycin (syr) and syringopeptin (syp) gene clusters are localized to this fragment. The syr and syp gene clusters encompass approximately 55 kb and approximately 80 kb, respectively. Both phytotoxins are synthesized by a thiotemplate mechanism of biosynthesis, requiring large multienzymatic proteins called peptide synthetases. Genes encoding peptide synthetases were identified within the syr and syp gene clusters, accounting for 90% of the DraI fragment. In addition, genes encoding regulatory and secretion proteins were localized to the DraI fragment. In particular, the salA gene, encoding a regulatory element responsible for syringomycin production and lesion formation in P. syringae pv. syringae strain B728a, was localized to the syr gene cluster. A putative ATP-binding cassette (ABC) transporter homolog was determined to be physically located in the syp gene cluster, but phenotypically affects production of both phytotoxins. Preliminary size estimates of the syr and syp gene clusters indicate that they represent two of the largest nonribosomal peptide synthetase gene clusters. Together, the syr and syp gene clusters encompass approximately 135 kb of DNA and may represent a genomic island in P. syringae pv. syringae that contributes to virulence in plant hosts.
引用
收藏
页码:1426 / 1435
页数:10
相关论文
共 58 条
[1]   The Pseudomonas syringae Hrp pathogenicity island has a tripartite mosaic structure composed of a cluster of type III secretion genes bounded by exchangeable effector and conserved effector loci that contribute to parasitic fitness and pathogenicity in plants [J].
Alfano, JR ;
Charkowski, AO ;
Deng, WL ;
Badel, JL ;
Petnicki-Ocwieja, T ;
van Dijk, K ;
Collmer, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (09) :4856-4861
[2]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[3]  
Ausubel F., 1990, CURRENT PROTOCOLS MO
[4]   Solution conformation of the Pseudomonas syringae pv syringae phytotoxic lipodepsipeptide syringopeptin 25-A - Two-dimensional NMR, distance geometry and molecular dynamics [J].
Ballio, A ;
Bossa, F ;
DiGiorgio, D ;
DiNola, A ;
Manetti, C ;
Paci, M ;
Scaloni, A ;
Segre, AL .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1995, 234 (03) :747-758
[5]   Pseudomonas syringae phytotoxins:: Mode of action, regulation, and biosynthesis by peptide and polyketide synthetases [J].
Bender, CL ;
Alarcón-Chaidez, F ;
Gross, DC .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 1999, 63 (02) :266-+
[6]   The complete genome sequence of Escherichia coli K-12 [J].
Blattner, FR ;
Plunkett, G ;
Bloch, CA ;
Perna, NT ;
Burland, V ;
Riley, M ;
ColladoVides, J ;
Glasner, JD ;
Rode, CK ;
Mayhew, GF ;
Gregor, J ;
Davis, NW ;
Kirkpatrick, HA ;
Goeden, MA ;
Rose, DJ ;
Mau, B ;
Shao, Y .
SCIENCE, 1997, 277 (5331) :1453-+
[7]  
Bradbury J.F., 1986, Guide to Plant Pathogenic Bacteria, P175
[8]  
Bultreys A, 1999, APPL ENVIRON MICROB, V65, P1904
[9]  
CAPONERO A, 1997, PSEUDOMONAS SYRINGAE, P202
[10]   SUPPRESSION OF ICE NUCLEATION-ACTIVE PSEUDOMONAS-SYRINGAE BY ANTAGONISTIC BACTERIA IN FRUIT TREE ORCHARDS AND EVALUATIONS OF FROST CONTROL [J].
CODY, YS ;
GROSS, DC ;
PROEBSTING, EL ;
SPOTTS, RA .
PHYTOPATHOLOGY, 1987, 77 (07) :1036-1044