CHARACTERIZATION AND TRANSCRIPTIONAL ANALYSIS OF THE GENE-CLUSTER FOR CORONAFACIC ACID, THE POLYKETIDE COMPONENT OF THE PHYTOTOXIN CORONATINE

被引:45
作者
LIYANAGE, H [1 ]
PALMER, DA [1 ]
ULLRICH, M [1 ]
BENDER, CL [1 ]
机构
[1] OKLAHOMA STATE UNIV,NOBLE RES CTR,DEPT PLANT PATHOL,STILLWATER,OK 74078
关键词
D O I
10.1128/AEM.61.11.3843-3848.1995
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Coronafacic acid (CFA), the polyketide component of the phytotoxin coronatine (COR), is activated and coupled to coronamic acid via amide bond formation, a biosynthetic step presumably catalyzed by the CFA ligase (cfl) gene product, The COR biosynthetic gene cluster in Pseudomonas syringae pv. glycinea PG4180 is located within a 32 kb region of a 90-kb plasmid designated p4180A, In the present study, a cloned region of p4180A complemented all CFA(-) mutants spanning an 18.8-kb region of the COR biosynthetic cluster. The genetic evidence presented in this study indicates that cfl and the CFA biosynthetic gene cluster are encoded by a single transcript and that transcription of all of the genes in this operon is directed by the cfl promoter, The cfl promoter was localized to a 0.37-kb region upstream of the transcriptional start site by progressive subcloning in pRG960sd, a vector containing a promoterless glucuronidase gene, Transcription of the cfl/CFA operon was temperature sensitive and showed maximal glucuronidase activity at 18 degrees C. Furthermore, transcription of the cfl/CFA operon was dependent on the functional activity of a modified two-component regulatory system located within the COR biosynthetic gene cluster. Thermoregulation of the cfl/CFA operon and the coronamic acid biosynthetic gene cluster via the modified two-component regulatory system is discussed.
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页码:3843 / 3848
页数:6
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