Nomenclature Abstract for Sphingomonas aromaticivorans Balkwill et al. 1997.

2003 ◽  
Author(s):  
Charles Thomas Parker ◽  
George M Garrity
Keyword(s):  
Sphingomonas Aromaticivorans

scholarly journals Identification and functional analysis of the genes for naphthalenesulfonate catabolism by Sphingomonas xenophaga BN6

Microbiology ◽  
2006 ◽  
Vol 152 (7) ◽  
pp. 1929-1940 ◽  
Author(s):  
Andreas Keck ◽  
Doris Conradt ◽  
Anette Mahler ◽  
Andreas Stolz ◽  
Ralf Mattes ◽  
...  
Keyword(s):  
Escherichia Coli ◽  
Functional Analysis ◽  
Degradative Pathway ◽  
Ferredoxin Reductase ◽  
Insertional Inactivation ◽  
Genes Encoding ◽  
Transcriptional Units ◽  
Dna Fragment ◽  
Sphingomonas Aromaticivorans ◽  
Sphingomonas Xenophaga

Sphingomonas xenophaga BN6 degrades various (substituted) naphthalenesulfonates to the corresponding (substituted) salicylates. A gene cluster was identified on the plasmid pBN6 which coded for several enzymes participating in the degradative pathway for naphthalenesulfonates. A DNA fragment of 16 915 bp was sequenced which contained 17 ORFs. The genes encoding the 1,2-dihydroxynaphthalene dioxygenase, 2-hydroxychromene-2-carboxylate isomerase, and 2′-hydroxybenzalpyruvate aldolase of the naphthalenesulfonate pathway were identified on the DNA fragment and the encoded proteins heterologously expressed in Escherichia coli. Also, the genes encoding the ferredoxin and ferredoxin reductase of a multi-component, ring-hydroxylating naphthalenesulfonate dioxygenase were identified by insertional inactivation. The identified genes generally demonstrated the highest degree of homology to enzymes encoded by the phenanthrene-degrading organism Sphingomonas sp. P2, or the megaplasmid pNL1 of the naphthalene- and biphenyl-degrading strain Sphingomonas aromaticivorans F199. The genes of S. xenophaga BN6 participating in the degradation of naphthalenesulfonates also shared the same organization in three different transcriptional units as the genes involved in the degradation of naphthalene, biphenyl, and phenanthrene previously found in Sphingomonas sp. P2 and S. aromaticivorans F199. The genes were flanked in S. xenophaga BN6 by ORFs which specify proteins that show the highest homologies to proteins of mobile genetic elements.

scholarly journals Complete Sequence of a 184-Kilobase Catabolic Plasmid from Sphingomonas aromaticivorans F199

1999 ◽  
Vol 181 (5) ◽  
pp. 1585-1602 ◽  
Author(s):  
Margaret F. Romine ◽  
Lisa C. Stillwell ◽  
Kwong-Kwok Wong ◽  
Sarah J. Thurston ◽  
Ellen C. Sisk ◽  
...  
Keyword(s):  
Aromatic Compounds ◽  
Efflux Pump ◽  
Gene Clusters ◽  
Complete Sequence ◽  
Open Reading Frames ◽  
Catabolic Plasmid ◽  
Associated Proteins ◽  
Replication Region ◽  
Sphingomonas Aromaticivorans ◽  
Large Clusters

ABSTRACT The complete 184,457-bp sequence of the aromatic catabolic plasmid, pNL1, from Sphingomonas aromaticivorans F199 has been determined. A total of 186 open reading frames (ORFs) are predicted to encode proteins, of which 79 are likely directly associated with catabolism or transport of aromatic compounds. Genes that encode enzymes associated with the degradation of biphenyl, naphthalene,m-xylene, and p-cresol are predicted to be distributed among 15 gene clusters. The unusual coclustering of genes associated with different pathways appears to have evolved in response to similarities in biochemical mechanisms required for the degradation of intermediates in different pathways. A putative efflux pump and several hypothetical membrane-associated proteins were identified and predicted to be involved in the transport of aromatic compounds and/or intermediates in catabolism across the cell wall. Several genes associated with integration and recombination, including two group II intron-associated maturases, were identified in the replication region, suggesting that pNL1 is able to undergo integration and excision events with the chromosome and/or other portions of the plasmid. Conjugative transfer of pNL1 to another Sphingomonas sp. was demonstrated, and genes associated with this function were found in two large clusters. Approximately one-third of the ORFs (59 of them) have no obvious homology to known genes.

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