1998
DOI: 10.1016/s0922-338x(98)80072-x
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Cloning and sequencing of a gene cluster for the Meta-cleavage pathway of aniline degradation in Acinetobacter sp. strain YAA

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Cited by 30 publications
(21 citation statements)
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“…Based on the hydroquinone degradation experiments reported above, HapE is assigned to be an NAD ϩ -dependent dehydrogenase (EC 1.2.1.61) that converts 4-hydroxymuconic semialdehyde to maleylacetate. Interestingly, HapE shows 37 to 43% sequence identity with 2-hydroxymuconic semialdehyde dehydrogenases, which are involved in the meta-cleavage pathways of catechol degradation (66,80). There is no other sequence of a 4-hydroxymuconic semialdehyde dehydrogenase known.…”
Section: Resultsmentioning
confidence: 99%
“…Based on the hydroquinone degradation experiments reported above, HapE is assigned to be an NAD ϩ -dependent dehydrogenase (EC 1.2.1.61) that converts 4-hydroxymuconic semialdehyde to maleylacetate. Interestingly, HapE shows 37 to 43% sequence identity with 2-hydroxymuconic semialdehyde dehydrogenases, which are involved in the meta-cleavage pathways of catechol degradation (66,80). There is no other sequence of a 4-hydroxymuconic semialdehyde dehydrogenase known.…”
Section: Resultsmentioning
confidence: 99%
“…First, to use as a reporter gene, a DNA fragment of approximately 1.0 kb containing a catechol 2,3-dioxygenase (C23O) gene (atdB) of Acinetobacter sp. strain YAA (42,45) was amplified by PCR using KOD DNA polymerase (Toyobo, Osaka, Japan), which produces blunt ends on the amplified fragment. The PCR mixture contained 0.…”
Section: Methodsmentioning
confidence: 99%
“…The PCR mixture contained 0. (42,45) was inserted into the StuI site and the EcoRV site of pKPN3 as a reporter gene to construct pKPN32 and pKPN35, respectively. For the disruption of nphR, a tetracycline resistance gene (tet) from pBR322 (4) was introduced into the EcoRV site of pKPN32 to construct pKPN33.…”
Section: Methodsmentioning
confidence: 99%
“…YAA. 7,8) The ORFs were organized as well as the alignments of the tdn and atd genes. On the basis of these results, it was concluded that ORF1 to 5 and ORF6 were tdnQTA1A2B and tdnR, respectively, encoding AD components and a LysR-type regulator.…”
Section: Gene Cloning and Sequence Analysismentioning
confidence: 99%
“…[2][3][4][5] Furthermore, genes encoding aniline dioxygenases (AD), catalyzing the conversion of aniline to catechol, have been cloned from Pseudomonas putida UCC22, 6) Acinetobacter sp. YAA, 7,8) and Pseudomonas sp. AW-2, 9) which metabolize aniline via the meta-cleavage pathway.…”
mentioning
confidence: 99%