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Announcement
4 January 2018

Draft Genome Sequences of Pseudomonas putida UV4 and UV4/95, Toluene Dioxygenase-Expressing Producers of cis-1,2-Dihydrodiols

ABSTRACT

Here, we present draft genome sequences of Pseudomonas putida strains UV4 and UV4/95, which demonstrate an ability to conduct a wide range of industrially important biotransformations of arenes, alkenes, and phenols.

GENOME ANNOUNCEMENT

In a series of pioneering studies, Gibson et al. discovered that Pseudomonas putida strains can oxidize certain aromatic hydrocarbons, such as benzene (1) and toluene, producing an enantiomerically pure cis-dihydrodiol (2). Further research by Imperial Chemical Industries (ICI) led to the discovery of P. putida NCIMB 11767, a toluene dioxygenase-expressing wild-type strain, from which the UV4 mutant was later derived and used in commercial (3) and biotechnological (4, 5) applications.
Two isolates of the P. putida UV4 strain were used for genome sequencing in this study, P. putida UV4, which was acquired from Stephen Taylor (ICI Biological Products) in 1984 and has been continuously cultured in the laboratory since that time, and P. putida UV4/95, which was subsampled from the main culture of P. putida UV4 in 1995 and preserved as a lyophilized sample until being revived for sequencing in 2015.
Bacterial cell cultures were grown overnight in LB medium at 30°C with 140-rpm shaking. Genomic DNA was extracted using the PowerSoil DNA isolation kit (Mo Bio, Inc., Carlsbad, CA, USA). Whole-genome sequencing was performed at MR DNA (Shallowater, TX, USA) using the Illumina MiSeq platform (2 × 150 bp), and sequence reads were assembled using NGen DNA assembly software (DNAStar, Inc., Madison, WI, USA) at the site. The assembly produced 31 contigs for UV4 and 34 contigs for UV4/95 with an average coverage of 40×, and an assessment with CheckM (6) characterized the draft genomes as 100% complete. The assemblies were annotated online using the NCBI Prokaryotic Genome Annotation Pipeline (PGAP) (7).
The draft genomes of both isolates have a GC content of 61.6%, with UV4/95 being longer (6.2 Mb versus 6.1 Mb for UV4). The total number of genes in UV4 was 5,703, while 5,790 genes were detected in UV4/95. Application of the species identification tool SpecI (8) identified P. putida F1 (1) as the closest related strain. A comparative analysis of the UV4 and UV4/95 draft genomes with P. putida F1 using Mauve (9) revealed the absence of a 90-kb-long region in UV4 and F1 compared to UV4/95, which was later identified as a genomic island by IslandViewer (10). The genomic island contains 88 genes, the majority of which are of unknown function or related to phage proteins.
A detailed functional annotation of protein-coding genes with RASTtk (11) assigned 35% of them to functional categories of SEED subsystems. A number of genes involved in the functionalization of aromatic compounds were detected, with dioxygenases and monooxygenases among them. Analysis with antiSMASH version 4.0 (12) predicted 40 biosynthetic clusters in UV4/95 and 42 in UV4.
P. putida strain UV4 has substantial enzymatic potential and is widely used in biotechnological applications. The reconstruction of its genomic sequence significantly improves our understanding of its physiological and biochemical peculiarities and provides new options for genetic manipulation of this microorganism in industrial and academic settings.

Accession number(s).

The annotated draft genome sequences of P. putida UV4 and UV4/95 have been deposited at NCBI GenBank under the accession numbers NHBB00000000 and NHBC00000000, respectively.

ACKNOWLEDGMENTS

This work was partly funded by the Leverhulme Trust and the Agri-Food Quest Competence Centre (AFQCC) at Queen’s University Belfast, United Kingdom.

REFERENCES

1.
Gibson DT, Koch JR, Kallio RE. 1968. Oxidative degradation of aromatic hydrocarbons by microorganisms. I. Enzymatic formation of catechol from benzene. Biochemistry 7:2653–2662.
2.
Gibson DT, Hensley M, Yoshioka H, Mabry TJ. 1970. Formation of (+)-cis-2,3-dihydroxy-1-methylcyclohexa-4,6-diene from toluene by Pseudomonas putida. Biochemistry 9:1626–1630.
3.
Ballard DGH, Courtis A, Shirley IM, Taylor SC. 1983. A biotech route to polyphenylene. J Chem Soc, Chem Commun 1983:954–955.
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Howard PW, Stephenson GR, Taylor SC. 1988. Convenient access to homochiral tricarbonyliron complexes. J Chem Soc, Chem Commun 1988:1603–1604.
5.
Allen CCR, Boyd DR, Dalton H, Sharma ND, Brannigan I, Kerley NA, Sheldrake GN, Taylor SC. 1995. Enantioselective bacterial biotransformation routes to cis-diol metabolites of monosubstituted benzenes, naphthalene and benzocycloalkenes of either absolute configuration. J Chem Soc, Chem Commun 1995:117–118.
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Parks DH, Imelfort M, Skennerton CT, Hugenholtz P, Tyson GW. 2015. CheckM: assessing the quality of microbial genomes recovered from isolates, single cells, and metagenomes. Genome Res 25:1043–1055.
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Tatusova T, Dicuccio M, Badretdin A, Chetvernin V, Nawrocki EP, Zaslavsky L, Lomsadze A, Pruitt KD, Borodovsky M, Ostell J. 2016. NCBI prokaryotic genome annotation pipeline. Nucleic Acids Res 44:6614–6624.
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Mende DR, Sunagawa S, Zeller G, Bork P. 2013. Accurate and universal delineation of prokaryotic species. Nat Methods 10:881–884.
9.
Darling ACE, Mau B, Blattner FR, Perna NT. 2004. Mauve: multiple alignment of conserved genomic sequence with rearrangements. Genome Res 14:1394–1403.
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Dhillon BK, Laird MR, Shay JA, Winsor GL, Lo R, Nizam F, Pereira SK, Waglechner N, McArthur AG, Langille MGI, Brinkman FSL. 2015. IslandViewer 3: more flexible, interactive genomic island discovery, visualization and analysis. Nucleic Acids Res 43:W104–W108.
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Brettin T, Davis JJ, Disz T, Edwards RA, Gerdes S, Olsen GJ, Olson R, Overbeek R, Parrello B, Pusch GD, Shukla M, Thomason JA, Stevens R, Vonstein V, Wattam AR, Xia F. 2015. RASTtk: a modular and extensible implementation of the RAST algorithm for building custom annotation pipelines and annotating batches of genomes. Sci Rep 5:8365.
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Weber T, Blin K, Duddela S, Krug D, Kim HU, Bruccoleri R, Lee SY, Fischbach MA, Müller R, Wohlleben W, Breitling R, Takano E, Medema MH. 2015. antiSMASH 3.0–a comprehensive resource for the genome mining of biosynthetic gene clusters. Nucleic Acids Res 43:W237–W243.

Information & Contributors

Information

Published In

cover image Genome Announcements
Genome Announcements
Volume 6Number 14 January 2018
eLocator: 10.1128/genomea.01419-17
PubMed: 29301889

History

Received: 13 November 2017
Accepted: 14 November 2017
Published online: 4 January 2018

Contributors

Authors

School of Biological Sciences, Queen’s University Belfast, Belfast, United Kingdom
Patrick Hoering
School of Biological Sciences, Queen’s University Belfast, Belfast, United Kingdom
Ksenia Arkhipova
School of Biological Sciences, Queen’s University Belfast, Belfast, United Kingdom
Present address: Ksenia Arkhipova, Theoretical Biology and Bioinformatics, Utrecht University, Utrecht, the Netherlands.
Roger C. Whitehead
School of Chemistry, University of Manchester, Manchester, United Kingdom
Derek R. Boyd
School of Chemistry and Chemical Engineering, Queen’s University Belfast, Belfast, United Kingdom
Christopher C. R. Allen
School of Biological Sciences, Queen’s University Belfast, Belfast, United Kingdom

Notes

Address correspondence to Christopher C. R. Allen, [email protected].

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