Genome Sequence of an Indigoid-Producing Strain, Pseudomonas sp. PI1

Pseudomonas sp. strain PI1 can cometabolize indole in the presence of phenol to produce various indigoids. Here, we present a 7.2-Mb draft genome sequence of strain PI1, which may provide insight into the study of phenol-indole cometabolism and its application in aromatic bioremediation and wastewater treatment processes.

and pharmaceutical industries. Compared with plant extraction and chemical synthesis, microbial production of indigoids has attracted much attention due to the merits of environmentally benign and mild reaction conditions (1,2). Numerous wide microorganisms can convert indole into indigo with or without the coexistence of aromatic compounds (3)(4)(5). Among the various microbial resources, phenol-degrading strains showed unique characteristics (5). For example, Acinetobacter sp. ST-500 can produce relatively high indigo yields in diphenylmethane-water twophase systems (6). Phenol hydroxylase from Pseudomonas sp. KL33 and Pseudomonas sp. KL28 catalyzed the production of various indigoid dyestuffs and hydroxyindoles from indole derivatives (7). Previously, we also cloned and expressed a novel phenol hydroxylase from Arthrobacter sp. W1 and revealed a novel indigoid formation pathway (8). Recently, a Gram-negative phenoldegrading bacterial strain named PI1 was isolated from lab bioreactors. It was identified as a member of the genus Pseudomonas according to 16S rRNA gene analysis. Pseudomonas sp. PI1 can cometabolize indole in the presence of phenol but cannot use indole as the sole carbon source (9). Application of liquidchromatography time-of-flight mass spectrometry revealed four products with an m/z of 262.067, all of which had the same molecular formula with indigo, i.e., C 16 H 10 N 2 O 2 . Results also showed that the proportion of the products varied with different indole concentrations. All these results indicate that new pathways exist for indole cometabolism in strain PI1. The genome report of strain PI1 will provide genetic information for exploring phenolindole cometabolism study.
The genome sequence of Pseudomonas sp. PI1 was obtained using an Illumina HiSeq-2000 sequencer (101 bp for each read). The reads were assembled de novo into 105 contigs using Velvet 1/2/10 software (10). The genome annotation was performed using the Rapid Annotations using Subsystems Technology (RAST) annotation server (11). The genome sequence of strain PI1 is 7,164,172 bp in length. A total of 6,288 candidate protein-coding sequences (CDSs) were predicted with coding intensity of 83.1%. There are 550 subsystems and 61 RNA genes present in the genome sequence.
The complete dmpKLMNOP components were identified in the genome, and dmpN showed 80% similarity with that of Pseudomonas sp. CF600 and Pseudomonas sp. KL33, suggesting that they might have similar indole transformation properties which needed further verification. In addition, a total of 225 CDSs were annotated for metabolism of aromatic compounds including biphenyl, salicylate, benzoate, p-hydroxybenzoate, and chloroaromatics. Interestingly, a rich set of annotated CDSs (107) were responsible for nitrogen metabolism, among which, 40 were for denitrification and 30 for ammonia assimilation, implying that strain PI1 might be a promising aerobic denitrifying bacterium that could be used in wastewater treatment processes. The genome information of strain PI1 reported here will provide sufficient information for the study of phenol-indole cometabolism and its application in aromatic bioremediation and wastewater treatment processes.
Nucleotide sequence accession numbers. This whole-genome shotgun project has been deposited at DDBJ/EMBL/GenBank under the accession no. JWMC00000000. The version described in this paper is the first version, JWMC00000000.1.

ACKNOWLEDGMENTS
This work was supported by the National Natural Science Foundation of China (21176040), the Program for New Century Excellent Talents in University (NCET-13-0077), and the Fundamental Research Funds for the Central Universities (DUT14YQ107). This work was also supported in part by grants from the Chinese National Science Foundation for Excellent Young Scholars (31422004).