Cloning and characterization of two catechol 1,2-dioxygenase genes from Acinetobacter radioresistens S13

被引:35
作者
Caposio, P
Pessione, E
Giuffrida, G
Conti, A
Landolfo, S
Giunta, C
Gribaudo, G
机构
[1] Univ Turin, Dept Microbiol & Publ Hlth, I-10126 Turin, Italy
[2] Univ Turin, Dept Human & Anim Biol, I-10126 Turin, Italy
[3] CNR, CSAAPZ, Canavese, Italy
关键词
Acinetobacter radioresistens S13; catechol 1,2-dioxygenase; expression patterns;
D O I
10.1016/S0923-2508(01)01290-6
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Two novel catechol 1,2-dioxygenase (C 1,2-O) genes have been isolated from an Acinetobacter radioresistens strain that grows on phenol or benzoate as sole carbon and energy source. Designated as catA(A) and catA(B), they encode proteins composed of 314 and 306 amino acids, whose deduced sequences indicate that they have approximately 53% identity, whereas their NH2-terminal and COOH-terminal regions have no sequences in common. This may explain their different thermal and pH stability. Polyclonal antibodies raised against an amino-terminal CatA(A) peptide or the whole CatA(B) protein were used to establish their inducible and differential expression patterns upon bacterial growth in phenol or benzoate. The CatAA protein (IsoA) was induced by both phenol and benzoate though with different kinetics, whereas the catAB product (IsoB) was constitutively produced at low levels that increased only during growth in the presence of benzoate. (C) 2002 Editions scientifiques et medicales Elsevier SAS. All rights reserved.
引用
收藏
页码:69 / 74
页数:6
相关论文
共 36 条
[1]  
Ausubel FM, 1994, CURRENT PROTOCOL MOL
[2]  
Barkay T, 1999, APPL ENVIRON MICROB, V65, P2697
[3]   NahW, a novel, inducible salicylate hydroxylase involved in mineralization of naphthalene by Pseudomonas stutzeri AN10 [J].
Bosch, R ;
Moore, ERB ;
García-Valdés, E ;
Pieper, DH .
JOURNAL OF BACTERIOLOGY, 1999, 181 (08) :2315-2322
[4]   Purification, biochemical properties and substrate specificity of a catechol 1,2-dioxygenase from a phenol degrading Acinetobacter radioresistens [J].
Briganti, F ;
Pessione, E ;
Giunta, C ;
Scozzafava, A .
FEBS LETTERS, 1997, 416 (01) :61-64
[5]   Purification and catalytic properties of two catechol 1,2-dioxygenase isozymes from benzoate-grown cells of Acinetobacter radioresistens [J].
Briganti, F ;
Pessione, E ;
Giunta, C ;
Mazzoli, R ;
Scozzafava, A .
JOURNAL OF PROTEIN CHEMISTRY, 2000, 19 (08) :709-716
[6]   Regulation of benzoate degradation in Acinetobacter sp. strain ADP1 by BenM, a LysR-Type transcriptional activator [J].
Collier, LS ;
Gaines, GL ;
Neidle, EL .
JOURNAL OF BACTERIOLOGY, 1998, 180 (09) :2493-2501
[7]   Mutations in catB, the gene encoding muconate cycloisomerase, activate transcription of the distal ben genes and contribute to a complex regulatory circuit in Acinetobacter sp strain ADP1 [J].
Cosper, NJ ;
Collier, LS ;
Clark, TJ ;
Scott, RA ;
Neidle, EL .
JOURNAL OF BACTERIOLOGY, 2000, 182 (24) :7044-7052
[8]   GENETIC ORGANIZATION, NUCLEOTIDE-SEQUENCE AND REGULATION OF EXPRESSION OF GENES ENCODING PHENOL HYDROXYLASE AND CATECHOL 1,2-DIOXYGENASE IN ACINETOBACTER-CALCOACETICUS NCIB8250 [J].
EHRT, S ;
SCHIRMER, F ;
HILLEN, W .
MOLECULAR MICROBIOLOGY, 1995, 18 (01) :13-20
[9]   RPON (SIGMA(54)) IS REQUIRED FOR CONVERSION OF PHENOL TO CATECHOL IN ACINETOBACTER-CALCOACETICUS [J].
EHRT, S ;
ORNSTON, LN ;
HILLEN, W .
JOURNAL OF BACTERIOLOGY, 1994, 176 (12) :3493-3499
[10]   Characterization of catechol catabolic genes from Rhodococcus erythropolis 1CP [J].
Eulberg, D ;
Golovleva, LA ;
Schlomann, M .
JOURNAL OF BACTERIOLOGY, 1997, 179 (02) :370-381