ABSTRACT
Here, we report the high-quality draft genome sequences of four phylogenetically diverse lignocellulose-degrading bacteria isolated from tropical soil (Gordonia sp., Paenibacillus sp., Variovorax sp., and Vogesella sp.) to elucidate the genetic basis of their ability to degrade lignocellulose. These isolates may provide novel enzymes for biofuel production.
GENOME ANNOUNCEMENT
Previous studies have shown that plant litter decomposition can occur rapidly in tropical forests (1). The strains presented here were cultivated under oxic conditions from the soil of the Luqillo Experimental Forest in Puerto Rico using lignin or cellulose in minimal media agar (2). These strains were selected for genome sequencing based on their ability to degrade model carbohydrates or phenolics (2).
The genomes were sequenced by the Joint Genome Institute using Illumina sequencing technology. The short and long paired-end library preparation and assembly followed the methodology previously described by Everroad et al. (3). To raise the quality of the final sequence, PCR PacBio consensus sequences were used to close gaps. The total amount of data from the Illumina reads ranged from 3.9 to 5.7 Mb per isolate. The average G+C content was between 50 and 67%. Variovorax sp. had the largest estimated genome at 7.7 Mb. The genome sizes of Gordonia sp. and Paenibacillus sp. were fairly similar at about 6.9 Mb and 6.3 Mb, respectively. Vogesella sp. had the smallest genome size at 4.2 Mb (Table 1).
Metadata of Puerto Rican soil strains and sequencing run details
The genomes possess genes related to lignocellulose degradation. Genomes of three bacterial strains isolated on alkali lignin (Variovorax sp., Gordonia sp., and Vogesella sp.) possess the beta-ketoadipate pathway for aromatic catabolism of lignin monomers and other phenolics into tricarboxylic acid cycle intermediates (4). Variovorax sp. and Gordonia sp. have multiple dioxygenases to metabolize two different aromatic catabolism intermediates (protocatechuate and catechol), while Vogesella sp. only has genes for protocatechuate degradation. Paenibacillus sp., the strain isolated on carboxymethyl cellulose in minimal media, possesses five different endo-1,4-betaxylanses. One or more of these xylanases could be highly active, as Paenibacillus sp. grows well on cellulose and xylan agar and degrades beta-d-glucopyranoside at notable rates.
Variovorax sp. and Vogesella sp. may also contribute to nitrogen cycling. Variovorax sp. has nitrogenases (nifK, nifD, and nifH) that are related to nitrogen fixation. Vogesella sp. has genes encoding respiratory nitrate reductase (alpha, beta, and gamma subunits) that are related to dissimilatory nitrate reduction.
All four genomes are part of an ongoing investigation of the genetic basis of lignocellulose degradation in tropical soils. These genomes will be compared to other genomes of lignocellulose-degrading bacteria from tropical forest environments, such as Enterobacter lignolyticus SCF1 (5), Klebsiella sp. BRL6-2 (6), and Burkholderia sp. LIG30 (7). The discovery of genes encoding lignocellulose-degrading enzymes would benefit biofuel production, for which lignocellulosic biomasses must be rapidly deconstructed and saccharified using enzymes.
Accession number(s).The whole-genome sequences reported here were deposited in DDBJ/EMBL/GenBank under the accession numbers listed in Table 1. Vogesella sp. LIG4 was originally submitted in 2012 as Pseudogulbankiania sp. LIG4, another Neisserales species, but has since been determined to be more closely related to other Vogesella sp. strains by 16S rRNA gene analyses with BLASTn and average nucleotide identity by BLAST (ANIb).
ACKNOWLEDGMENTS
Work conducted by the Joint Bioenergy Institute was supported by the Office of Science, Office of Biological and Environmental Research, of the U.S. Department of Energy under contract number DE-AC02-05CH11231. This material is also based upon work supported by the National Science Foundation Graduate Research Fellowship Program under grant number DGE-1452154.
FOOTNOTES
- Received 11 March 2017.
- Accepted 15 March 2017.
- Published 4 May 2017.
- Copyright © 2017 Woo et al.
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