Complete genome sequence of Planctomyces brasiliensis type strain (DSM 5305T), phylogenomic analysis and reclassification of Planctomycetes including the descriptions of Gimesia gen. nov., Planctopirus gen. nov. and Rubinisphaera gen. nov. and emended descriptions of the order Planctomycetales and the family Planctomycetaceae
- Carmen Scheuner1,
- Brian J Tindall1,
- Megan Lu2, 3,
- Matt Nolan2,
- Alla Lapidus2,
- Jan-Fang Cheng2,
- Lynne Goodwin2, 3,
- Sam Pitluck2,
- Marcel Huntemann2,
- Konstantinos Liolios2,
- Ioanna Pagani2,
- Konstantinos Mavromatis2,
- Natalia Ivanova2,
- Amrita Pati2,
- Amy Chen4,
- Krishna Palaniappan4,
- Cynthia D Jeffries2, 5,
- Loren Hauser2, 5,
- Miriam Land2, 5,
- Romano Mwirichia6,
- Manfred Rohde7,
- Birte Abt1,
- John C Detter2, 3,
- Tanja Woyke2,
- Jonathan A Eisen2, 8,
- Victor Markowitz4,
- Philip Hugenholtz2, 9,
- Markus Göker1Email author,
- Nikos C Kyrpides2, 10 and
- Hans-Peter Klenk1
© Scheuner et al.; licensee BioMed Central Ltd. 2014
Received: 12 June 2014
Accepted: 16 June 2014
Published: 8 December 2014
Planctomyces brasiliensis Schlesner 1990 belongs to the order Planctomycetales, which differs from other bacterial taxa by several distinctive features such as internal cell compartmentalization, multiplication by forming buds directly from the spherical, ovoid or pear-shaped mother cell and a cell wall consisting of a proteinaceous layer rather than a peptidoglycan layer. The first strains of P. brasiliensis, including the type strain IFAM 1448T, were isolated from a water sample of Lagoa Vermelha, a salt pit near Rio de Janeiro, Brasil. This is the second completed genome sequence of a type strain of the genus Planctomyces to be published and the sixth type strain genome sequence from the family Planctomycetaceae. The 6,006,602 bp long genome with its 4,811 protein-coding and 54 RNA genes is a part of the G enomic E ncyclopedia of Bacteria and Archaea project. Phylogenomic analyses indicate that the classification within the Planctomycetaceae is partially in conflict with its evolutionary history, as the positioning of Schlesneria renders the genus Planctomyces paraphyletic. A re-analysis of published fatty-acid measurements also does not support the current arrangement of the two genera. A quantitative comparison of phylogenetic and phenotypic aspects indicates that the three Planctomyces species with type strains available in public culture collections should be placed in separate genera. Thus the genera Gimesia, Planctopirus and Rubinisphaera are proposed to accommodate P. maris, P. limnophilus and P. brasiliensis, respectively. Pronounced differences between the reported G + C content of Gemmata obscuriglobus, Singulisphaera acidiphila and Zavarzinella formosa and G + C content calculated from their genome sequences call for emendation of their species descriptions. In addition to other features, the range of G + C values reported for the genera within the Planctomycetaceae indicates that the descriptions of the family and the order should be emended.
Strain IFAM 1448T (=DSM 5305 = ATCC 49424 = JCM 21570) is the type strain of Planctomyces brasiliensis. Although the genus currently consists of six species with validly published names, only three of them, P. brasiliensis, P. limnophilus, and P. maris contain cultured type strains [1–3]. The other three species, including the type species P. bekefii  as well as P. stranskae and P. guttaeformis  are to date not represented by cultured strains and have been described solely on the basis of their morphological properties , with the descriptions and illustrations serving as the type material. P. bekefii was initially described as a fungus under the International Code of Botanical Nomenclature [4, 7]. The genus name derives from the Greek words ‘planktos’, wandering, floating, and ‘mukês’ meaning ‘fungus’ to indicate a floating fungus , reflecting their initial descriptions as members of the fungi. The species epithet ‘brasiliensis’ is a Latin masculine adjective that means “of or belonging to Brazil” . Strain IFAM 1448T together with other strains designated IFAM 1450, IFAM 1454 and IFAM 1456 were isolated from water samples collected in November 1982 from Lagoa Vermelha, a salt pit at the Atlantic coast north of Rio de Janeiro, Brazil . Another strain (DSM 11908) potentially belonging to P. brasiliensis was isolated from postlarvae of the Giant Tiger Prawn, Penaeus monodon, infected with the monodon baculovirus .
The similarity of genes of both cultured and uncultured Planctomyces species has been studied not only based on 16S rRNA gene sequences, but also using the RNase P RNA genes . The unique compartmentalized cell structure shared by all Planctomycetes investigated so far is remarkable , as is the relatively large size of Planctomycetes genomes, which could be attributed to their free-living lifestyles . The membrane organization of organisms belonging to the Planctomycetes, Verrucomicrobia and Chlamydiae superphylum is currently the subject of intense discussion in the literature, e.g. as an exception to  or as a variation of  the classical Gram-negative cell plan. P. limnophilus has been established as model organism for the phylum, as it is the first and only species of Planctomycetes that has been genetically modified [13, 14]. Here we present a summary classification and a set of features for P. brasiliensis IFAM 1448T, together with the description of the complete genomic sequencing and annotation, as well as a re-assessment of the taxonomy of the group based on phylogenomic as well as traditionally sampled characters.
Classification and features
16S rRNA gene analysis
A representative genomic 16S rRNA gene sequence of strain DSM 5305T was compared with the Greengenes database for determining the weighted relative frequencies of taxa and (truncated) keywords as previously described . The most frequently occurring genus was Planctomyces (100.0%) (18 hits in total). Regarding the two hits to sequences from members of the species, the average identity within high-scoring segment pairs (HSPs) was 100.0%, whereas the average coverage by HSPs was 97.2%. Regarding the five hits to sequences from other members of the genus, the average identity within HSPs was 90.1%, whereas the average coverage by HSPs was 58.5%. Among all other species, the one yielding the highest score was P. maris, which corresponded to an identity of 90.3% and an HSP coverage of 63.5%. The highest-scoring environmental sequence was DQ015774 (‘Antarctic lake water clone ELB25-062’) , which showed an identity of 96.2% and an HSP coverage of 98.3%. The most frequently occurring keywords within the labels of environmental samples that yielded hits were ‘treatment’ (2.7%), ‘microbi’ (2.1%), ‘sediment’ (1.8%), ‘gut’ (1.8%) and ‘microbiom’ (1.7%) (232 hits in total). Environmental samples which yielded hits of a higher score than the highest scoring species were not found, which might indicate that P. brasiliensis is rarely found in the environment. But overall Planctomyces species have been isolated from an ecologically large variety of environments [2, 3], which is also reflected by the above most frequently occurring keywords.
Morphology and physiology
Species Planctomyces brasiliensis
Type strain DSM 5305
several sugars, such as D-cellobiose, maltose, trehalose
marine fresh water
water from salt pit
Lagoa Vermelha, Brazil
Sample collection time
0 m, sea level
Chemical analysis of the cell wall of P. brasiliensis showed that proteins are the principal constituents with a value of 79.9% of the dry weight . Detailed analysis of the protein composition indicated that the major amino acids were asparagine, threonine, serine, glutamine, proline, glycine and alanine . Total extractable lipids represent 10% of the cell dry weight of strain IFAM 1448T . The major fatty acids (>1%) are C16:0 (30.7%), C16:1 (25%), C18:1 (13.1%), C20:1 (9.9%), C15:0 (8.4%), C18:0 (5.6%), C14:0 (4.0%), C17:0 (1.3%) and C17:1 (1.8%) . A comparison with other representatives of the Planctomycetes is given below.
Genome sequencing and annotation
Genome project history
Genome sequencing project information
Three genomic libraries: one 454 pyrosequence standard library, one 454 PE library (14 kb insert size), one Illumina library
Illumina GAii, 454 GS FLX Titanium
124.8 × Illumina; 91.0 × pyrosequence
Newbler version 2.0.00.20-PostRelease-10-28-2008-g-3.4.6, phrap
Gene calling method
Prodigal 1.4, GenePRIMP
Genbank Date of Release
March 2, 2011
NCBI project ID
Source material identifier
Tree of Life, GEBA
Growth conditions and DNA isolation
A culture of DSM 5305T was grown in DSMZ medium 607 (M13 Verrucomicrobium medium)  at 30°C. DNA was isolated from 0.5-1 g of cell paste using Jetflex Genomic DNA Purification Kit (GENOMED 600100) following the standard protocol as recommended by the manufacturer: Cell lysis was enhanced by adding 20 μl proteinase K for two hours at 58°C. DNA is available through the DNA Bank Network .
Genome sequencing and assembly
The genome was sequenced using a combination of Illumina and 454 sequencing platforms. All general aspects of library construction and sequencing can be found at the JGI website . Pyrosequencing reads were assembled using the Newbler assembler (Roche). The initial Newbler assembly consisting of 53 contigs in one scaffold was converted into a Phrap assembly (http://www.phrap.com) making fake reads from the consensus, to collect the read pairs in the 454 paired-end library. Illumina GAii sequencing data (3,029.9 Mb) were assembled with Velvet  and the consensus sequences were shredded into 1.5 kb overlapped fake reads and assembled together with the 454 data. 454 draft assembly was based on 164.2 Mb 454 draft data and all of the 454 paired end data. Newbler parameters were -consed -a 50 -l 350 -g -m -ml 20. The Phred/Phrap/Consed software package (http://www.phrap.com/) was used for sequence assembly and quality assessment in the subsequent finishing process. After the shotgun stage, reads were assembled with parallel phrap (High Performance Software, LLC). Possible mis-assemblies were corrected with gapResolution (http://www.jgi.doe.gov/), Dupfinisher, or sequencing cloned bridging PCR fragments with subcloning or transposon bombing (Epicentre Biotechnologies, Madison, WI) . Gaps between contigs were closed by editing in Consed, by PCR and by Bubble PCR primer walks (J.-F. Chang, unpublished). A total of 156 additional reactions were necessary to close gaps and to raise the quality of the finished sequence. Illumina reads were also used to correct potential base errors and increase consensus quality using the Polisher software developed at JGI . The error rate of the completed genome sequence is less than one in 100,000. Together, the combination of the Illumina and 454 sequencing platforms provided 285.0 × coverage of the genome. The final assembly contained 281,884 pyrosequence and 39,867,623 Illumina reads.
Genes were identified using Prodigal  as part of the DOE-JGI  genome annotation pipeline, followed by a round of manual curation using the JGI GenePRIMP pipeline . The predicted CDSs were translated and used to search the National Center for Biotechnology Information (NCBI) nonredundant database, UniProt, TIGR-Fam, Pfam, PRIAM, KEGG, COG, and InterPro databases. Additional gene prediction analysis and functional annotation was performed within the Integrated Microbial Genomes - Expert Review (IMG-ER) platform .
% of total
Genome size (bp)
DNA coding region (bp)
DNA G + C content (bp)
Number of replicons
Genes with function prediction
Genes in paralog clusters
Genes assigned to COGs
Genes assigned Pfam domains
Genes with signal peptides
Genes with transmembrane helices
Number of genes associated with the general COG functional categories
Translation, ribosomal structure and biogenesis
RNA processing and modification
Replication, recombination and repair
Chromatin structure and dynamics
Cell cycle control, cell division, chromosome partitioning
Signal transduction mechanisms
Cell wall/membrane/envelope biogenesis
Intracellular trafficking, secretion, and vesicular transport
Posttranslational modification, protein turnover, chaperones
Energy production and conversion
Carbohydrate transport and metabolism
Amino acid transport and metabolism
Nucleotide transport and metabolism
Coenzyme transport and metabolism
Lipid transport and metabolism
Inorganic ion transport and metabolism
Secondary metabolites biosynthesis, transport and catabolism
General function prediction only
Not in COGs
Insights from the genome sequence
Taxonomic classification vs. 16S rRNA gene analysis of Planctomyces and Schlesneria
Although it has only slowly been appreciated by taxonomists after Darwin had published his seminal works, the sole possible goal of a taxonomic classification is to summarize the genealogy of the organisms [37, 51]. For this reason, it does not matter if a taxonomic classification contains less information than the empirical estimate of the phylogeny from which it was derived. But it does matter whether or not a classification can pretend to summarize the respective underlying genealogies – and this is never the case where classifications include obviously non-monophyletic groups [37, 51–53].
As indicated earlier , in this respect the current classification of Planctomycetes is only partially satisfactory because with the description of the genus Schlesneria the genus Planctomyces now appears to be paraphyletic in the 16S rRNA gene trees (see Figure 1 and [19–21, 54]), with P. limnophilus being more closely related to Schlesneria than to the other Planctomyces species. The two versions of the 16S rRNA gene sequence of Schlesneria paludicola MPL7T submitted to INSDC, NR_042466 and AM162407, are identical; AM162407 has been used in Figure 1. The previously published 16S rRNA gene sequences of P. limnophilus  and P. brasiliensis (this study) have also been found to be identical or almost identical to those from the respective genome-sequencing projects. For this reason, the biological identity of the Schlesneria and Planctomyces strains used can hardly be called into question, and a mix-up or contamination of cultures cannot explain the positioning of the strains in the phylogenetic analyses. In fact, that the establishment of the genus Schlesneria renders Planctomyces paraphyletic was, surprisingly, already visible in the phylogenetic tree presented in , even though support for the non-monophyly of Planctomyces is stronger in our analyses (Figure 1). (Since Kulichevskaya et al.  did not mention the issue of taxa being monophyletic this also cannot be considered to be a pre-requisite for their interpretation, even though it is then not entirely clear why they conducted a phylogenetic analysis in the first place.) This picture did not change after R + Y coding of the 16S rRNA gene alignment , which still yielded 97% support for the sister group of P. limnophilus and S. paludicola (data not shown).
To measure this phylogenetic conflict in detail, we conducted both unconstrained heuristic searches for the best tree under the maximum likelihood (ML)  and maximum parsimony (MP) criterion  as well as searches constrained for the monophyly of all genera (for details of the data matrix see the caption of Figure 1). The best-known ML tree had a log likelihood of −9,214.93, whereas the best tree found under the constraint had a log likelihood of −9,249.16. The constrained tree was significantly worse than the globally best one in the Shimodaira-Hasegawa test as implemented in RAxML  (α = 0.01). The best-known MP tree had a score of 1,519, whereas the best constrained trees found had a score of 1,541 and were significantly worse in the Kishino-Hasegawa test as implemented in PAUP*  (α = 0.05). (See, e.g. chapter 21 in  for an in-depth description of such paired-site tests.) Accordingly, the current classification within the family as used in, e.g.,  is in significant conflict with the 16S rRNA gene data.
In the following we will assess whether these 16S rRNA gene results can be confirmed with genomic data.
Phylogenomic analysis and comparative genomics
Genomic G + C content of the Planctomycetaceae type strains, including Phycisphaera mikurensis as outgroup
G + C content from species description [%]
G + C content calculated from genome sequence [%]
NCBI accessions/IMG taxon IDs (number of contigs)
Blastopirellula marina DSM 3645T
53.6 - 57.4 
AANZ00000000 (67); NZ_AANZ00000000 (4)*
Gemmata obscuriglobus UQM 2246T
64.4 ± 1.0 
Isosphaera pallida ATCC 43644T
Phycisphaera mikurensis NBRC 102666T
Pirellula staleyi DSM 6068T
56.4 ± 0.4 - 57.4 ± 0.3 
Planctomyces brasiliensis DSM 5305T
55.1 - 57.7 
Planctomyces limnophilus DSM 3776T
53.24 ± 0.59 
Planctomyces maris DSM 8797T
Rhodopirellula baltica SH 1T
Schlesneria paludicola DSM 18645T
AHZR00000000 (112); NZ_AHZR00000000 (24)*
Singulisphaera acidiphila DSM 18658T
AGRX00000000 (113); CP003364 - CP003367*
Zavarzinella formosa DSM 19928T
IMG ID: 2548877000 (594); NZ_AIAB00000000 (106)*
The G + C content calculated from the genome sequence of G. obscuriglobus was 67.18%, whereas the previously published value, determined using traditional techniques, is 64.4 ± 1.0% . Similarly, the G + C content of S. acidiphila was given as 59.9%  and that of Z. formosa was given as 62.5% , whereas the analysis of the genome sequences yields 62.23% and 59.10%, respectively. The three strongly deviating G + C values discovered here were all obtained using thermal denaturation [61, 67, 68]. A recent study  has shown that when calculated from genome sequences the G + C content varies at most 1% within species (which holds even though no attempt was made to remove plasmid sequences) and that larger variances are caused by the inaccuracies of the traditional techniques. It has thus been recommended to conduct emendations of species descriptions in the case of discrepancies larger than 1%, and to also conduct emendations of genus descriptions if the species emendations yield values that do not fit into the range of the G + C content given in the literature for the respective genus .
The G + C content of the Planctomycetaceae, using exact calculations from the genome sequences where possible, ranges from 50% to 70% (Table 5 and [70, 71]), similar to the range between 52% and 69% measured by Schlesner et al. using traditional methods . However, the description of the order Planctomycetales as well as the family Planctomycetaceae by Schlesner and Stackebrandt 1986 , who could at that time only consider the Pirellula staleyi, Pirellula marina (formerly Pirella), Planctomyces maris and Planctomyces limnophilus, refers to a G + C content of 50 to 59%. Planctomyces and Schlesneria have a comparatively low G + C content between 50% and 56%, with P. brasiliensis and P. maris differing more strongly from each other than P. limnophilus and S. paludicola. Similarly, Schlesner et al. reported a G + C content of 50 to 58% for Planctomyces strains . The G + C content of the group comprising Blastopirellula, Pirellula and Rhodopirellula ranges from 55% to 57%. Although the G + C content of Zavarzinella measured from the genome sequence is lower than the one given in the species description, the group containing Aquisphaera, Gemmata, Isosphaera, Singulisphaera, Telmatocola and Zavarzinella possesses a higher G + C content than the other Planctomycetaceae, between 59% and 70%.
The genome sequences (Table 5) were phylogenetically investigated using the DSMZ phylogenomics pipeline as previously described [72–75] using NCBI BLAST , TribeMCL , OrthoMCL , MUSCLE , RASCAL , GBLOCKS  and MARE  to generate gene- and ortholog-content matrices as well as concatenated alignments of distinct selections of genes. Maximum likelihood (ML)  and maximum-parsimony (MP) [84, 85] trees were inferred from the data matrices with RAxML [57, 86] and PAUP* , respectively, as previously described [72–75].
The phylogenomic tree (Figure 4) is topologically identical to the 16S rRNA gene tree (Figure 1) except for the backbone of the trees, which showed no support in the 16S rRNA gene analysis. Furthermore, the phylogenomic analysis confirms with maximum support the 16S rRNA tree that P. limnophilus and S. paludicola are sister taxa and, thus, Planctomyces is paraphyletic. The genomic interrelationships between these four species are thus examined more closely in the following. A genome sequence-based phylogeny with the same branching order but less bootstrapping support (probably because a restricted set of genes was used) was recently reported by Gou et al. .
The genomes of the four genome-sequenced Planctomyces and Schlesneria species differ significantly in their size. The genomes of S. paludicola (8.6 Mb, 6,860 protein-coding genes) and P. maris (7.8 Mb, 6,480 protein-coding genes) are significantly larger in size than the genomes of P. brasiliensis (6.0 Mb, 4,811 protein-coding genes) and P. limnophilus (5.5 Mb, 4,304 protein-coding genes).
Pairwise comparison of the four Planctomycetaceae species using GGDC, formula 2 (DDH estimates based on identities / HSP length)*
18.60% ± 2.27
21.40% ± 2.34
20.90% ± 2.33
18.60% ± 2.27
24.10% ± 2.39
23.20% ± 2.38
21.40% ± 2.34
24.10% ± 2.39
22.00% ± 2.35
20.90% ± 2.33
23.20% ± 2.38
22.00% ± 2.35
This comparison of the genomes revealed that P. brasiliensis shows a slightly higher DDH estimate with P. maris, compared to those with P. limnophilus and Schlesneria paludicola. For Schlesneria paludicola, a higher DDH value was estimated with P. limnophilus, in contrast to the other genomes. These results are in accordance with the 16S rRNA (Figure 1) and phylogenomic analyses (Figure 4). However, given the confidence intervals (Table 6), the DDH estimates do not show significant differences.
P. brasiliensis shares 63.1% of its clusters with P. maris, but only 57.6% and 58.2% clusters with P. limnophilus and S. paludicola, respectively. Only 27.5% of the P. brasiliensis genes have no homologs in the other genomes. P. limnophilus shares 63.2% of its clusters with S. paludicola, whereas P. brasiliensis shares 58.2% and P. maris shares 50.4% clusters with S. paludicola.
P. brasiliensis shares many more clusters of homologous genes with P. maris than with the other genomes. Of the four compared genomes, P. limnophilus shares most clusters of homologous genes with S. paludicola. These results are in accordance with the 16S rRNA (Figure 1) and phylogenomic analyses (Figure 4) as well as the GGDC results (Table 6).
Jeske et al.  performed a comprehensive genome mining approach to identify secondary metabolite related genes or gene clusters within the Planctomycetes. Just as in the other studied Planctomycetes, a number of genes putatively related with the production of secondary metabolites were identified in P. brasiliensis, that is, bacteriocin, ectoine, lantipeptide, terpene and type 1 polyketide synthases . The study revealed Planctomycetes as a rich source for small molecules that might ultimately lead to new antibiotics or drugs .
The measurements from allegedly the same strains did not always cluster together. Blastopirellula marina, P. maris and Rhodopirellula baltica showed distinct groupings of their respective measurements. The sum of the B. marina measurements from Schlesner et al.  is substantially below 100%, whereas the measurements of P. maris from Kerger et al.  sum up to much less than 100%, indicating missing or overstated values (Figure 6, all strong deviations of the sum from 100% denoted with asterisks). Omitting the questionable data in this respect did not alter the relative positioning of the other measurements (data not shown). The differences between the R. baltica measurements from two studies [36, 66] might be caused by the distinct growth conditions (temperature and medium). Except for these three species, the fatty-acid analyses of the Planctomycetes type strains appeared fairly reproducible (Figure 6).
The analysis of the fatty-acid measurements shows a group comprising P. brasiliensis, P. maris and S. paludicola (disregarding the incomplete P. maris data from ), whereas P. limnophilus does not cluster together with the other Planctomyces species. The analysis supports the earlier finding  that S. paludicola can be differentiated from P. limnophilus on the basis of the fatty acids. However, the analysis also shows that S. paludicola cannot be differentiated from P. brasiliensis and P. maris, whose fatty acids were not analyzed in . Rather, the fatty-acid profile of P. limnophilus differs from that of the other Planctomyces species (and Schlesneria), hence the overall similarity in fatty-acid profiles does not entirely reflect the relationships inferred from 16S rRNA gene (Figure 1) and phylogenomic analyses (Figure 4) as well as the GGDC results (Table 6). Thus the evidence for distinguishing Planctomyces and Schlesneria on the basis of fatty acids given by Kulichevskaya et al.  cannot be confirmed once all three Planctomyces species with cultivated type strains are considered, since the published fatty-acid profile of S. paludicola cannot be differentiated from that of P. brasiliensis and P. maris.
Taxonomy of the Planctomyces-Schlesneria complex
Given the positioning of the Planctomyces and Schlesneria species in the phylogenetic trees (Figure 1, Figure 4), several taxonomic changes could be conducted to render all genera monophyletic. The taxonomy of the group is apparently hampered by the unavailability of a culture of the type species, P. bekefii, which was described 90 years ago and based on a few morphological characters . In our view, the scarcity of published information on this species does not allow prediction of its phylogenetic position relative to the other species if a 16S rRNA gene sequence of P. bekefii could be obtained (Figure 1). For this reason, the only safeguard against the possibility that phylogenetic analysis of P. bekefii would keep Planctomyces monophyletic is to place all Planctomyces species with an already known 16S rRNA gene (or even genome) sequence into a genus of their own. Indeed, arguing against the removal of other Planctomyces species from the genus because the comparison with the type species using contemporary taxonomic methods is impossible would be illogical, because none of the other Planctomycetes genera with validly published names have been compared with P. bekefii using modern methods either. For instance, there is insufficient evidence against a sister-group relationship between P. bekefii and S. paludicola, which was described mainly based on the comparison with P. limnophilus .
Whether or not the three cultivated Planctomyces species and Schlesneria should be placed in one, two, three or four genera should also be assessed by comparing the divergence among the resulting taxa with those of others. For instance, it would be inconsistent to place all four species, or only two of them, in a single genus if less divergent groups within Planctomycetes existed that were nevertheless split into several genera. Divergence was measured directly from the phylogenetic trees (Figure 1, Figure 4) as the maximum subtree height (MaSH) of each subtree without its stem branch. This measure has the advantage that it is on the one hand equivalent to half the maximum pairwise (patristic) distance between organisms placed in a subtree of an ultrametric tree but on the other hand can also be applied if a phylogenetic tree is non-ultrametric, which is much more frequent (Figure 1, Figure 4). Indeed, pairwise distances can be taxonomically misleading because under non-ultrametric conditions less distant organisms need not be more closely related [38, 59, 69]. Using MaSH, the reference to subtrees guarantees by definition that only monophyletic groups are measured.
MaSH values calculated for the ML trees inferred in this study
16S rRNA gene
S. acidiphila, S. rosea*
B. cremea*, B. marina
P. brasiliensis, P. maris
P. limnophilus, Sc.
Aq.*, Is., S. acidiphila, S. rosea*
B. cremea*, B. marina, Pi.
Ge., Te.*, Za.
B. cremea*, B. marina, Pi., Rh.
Aq.*, Ge., Is., S. acidiphila, S. rosea*, Te.*, Za.
Aq.*, Ge., Is., Pl., Sc., S. acidiphila, S. rosea*, Te.*, Za.
Aq.*, B. cremea*, B. marina, Ge., Is., Pi., Pl., Rh., Sc., S. acidiphila, S. rosea*, Te.*, Za.
Aq.*, B. cremea*, B. marina, Ge., Is., Ph., Pi., Pl., Rh., Sc., S. acidiphila, S. rosea*, Te.*, Za.
Polar lipids 1
A. giovannonii 
B. cremea 
I. pallida 
S. acidiphila 
S. rosea 
We conclude that both genomic and phenotypic analyses according to both qualitative and quantitative criteria support the placement of the three Planctomyces species with cultivated type strains into genera separate from each other and from Schlesneria.
As explained in detail above, the differences in the reported G + C contents of G. obscuriglobus, S. acidiphila and Z. formosa from the ones calculated from their genome sequences justify an emendation of their species descriptions and in the case of Gemmata an emendation of the genus description (which referred to the G + C content).
Moreover, the range of G + C content values determined for the genera now placed within Planctomycetaceae (Planctomycetales) is in conflict with the description of the family (and order) as given by Schlesner and Stackebrandt 1986 . In addition, an optimal growth temperature of 41°C is reported for Isosphaera , which is considerably higher than the one reported in the description of the family (and order). For Schlesneria, Singulisphaera, Telmatocola and Zavarzinella a slightly lower optimal growth temperature is reported, i.e. 20°C upward [48, 55, 67, 68, 71]. Furthermore, for the genera Schlesneria and Zavarzinella it was reported that the daughter cells are motile by means of two  or one to two flagella , respectively, whereas the description of the family (and order) only considered the presence of one flagellum.
Whereas these discrepancies call for an emendation of the family Planctomycetaceae, phylogenomic (Figure 4) and 16S rRNA gene analyses (Figure 1) show a monophyletic group comprising the genera with high G + C content. The remaining genera appear unresolved in the 16S rRNA gene tree (Figure 1) but as a maximally supported clade comprising the genera Planctomyces, Schlesneria, Blastopirellula, Pirellula and Rhodopirellula in the phylogenomic tree (Figure 4). This would support a splitting of the quite heterogeneous Planctomycetaceae into two families, but the unknown position of the type species, P. bekefii, of the type genus means that a more narrowly defined Planctomycetaceae may not include P. bekefii. For this reason, we refrain from generating a novel family to accommodate the high-G + C genera.
Emended description of the genus Gemmata Franzmann and Skerman (1985)
The description is the one given by Franzmann and Skerman  with the following modification.
The G + C content is about 67%.
Emended description of the species Gemmata obscuriglobus Franzmann and Skerman (1985)
The description of the species Gemmata obscuriglobus is the one given by Franzmann and Skerman , with the following modification.
The G + C content is 67%.
Emended description of the species Singulisphaera acidiphila Kulichevskaya et al. (2008)
The description of the species Singulisphaera acidiphila is the one given by Kulichevskaya et al. (2008) , with the following modification.
The G + C content is 62%.
Emended description of the species Zavarzinella formosa Kulichevskaya et al. 2009
The description of the species Zavarzinella formosa is the one given by Kulichevskaya et al. (2009) , with the following modification.
The G + C content is 59%.
Emended description of the order Planctomycetales Schlesner and Stackebrandt 1986
The description of the order Planctomycetales is the one given by Schlesner and Stackebrandt , with the following modification.
Daughter cells may be motile by means of one or two flagella. The G + C content ranges between about 50% and about 70%. The growth temperature optimum ranges between 20°C and 40°C.
Emended description of the family Planctomycetaceae Schlesner and Stackebrandt 1986
The description of the family Planctomycetaceae is the one given by Schlesner and Stackebrandt , with the following modification.
Daughter cells may be motile by means of one or two flagella. The G + C content ranges between about 50% and about 70%. The growth temperature optimum ranges approximately between 20°C and 40°C.
Description of Rubinisphaera gen. nov
Rubinisphaera (Ru.bi.ni.sphaer’a N. L. fem. n. Rubinia named in honor of Edward Rubin, an American geneticist and medical researcher, who played a key role in initiating the Genomic Encyclopedia of Archaea and Bacteria project at the DOE Joint Genome Institute (JGI); NL fem. n. sphaerae, a ball, globe, sphere; N. L. fem. n. Rubinisphaera, a spherical organism named after Edward Rubin).
The features are the ones of the type species. Characteristic polyamines are sym-homospermidine and spermidine. The polar lipids phosphatidyl-monomethylethanolamine and phosphatidyl-dimethylethanolamine are absent. Major fatty acids are C16:0 and C16:1 ω7c. The G + C content is about 56%.
The type species is Rubinisphaera brasiliensis. Rubinisphaera belongs to Planctomycetaceae.
Description of Rubinisphaera brasiliensis(Schlesner 1990) comb. nov.
Rubinisphaera brasiliensis (bra.si.lien’sis L. m. adj. pertaining to the country of Brazil).
Basonym: Planctomyces brasiliensis Schlesner 1990.
The genus Rubinispharea is comprised of one species, Rubinisphaera brasiliensis. The characteristics of the species are given in the genus description and the description given by Schlesner (1989) .
The type strain is IFAM 1448T (=ATCC 49424 = DSM 5305 = JCM 21570 = NBRC 103401).
Description of Planctopirus gen. nov.
Planctopirus (Planc.to.pi’rus Gr. adj. planktos, wandering, floating; L. maS. n. pirus, a pear tree, referring to the shape of the cells, which also occur in bundles; NL fem. n. Planctopirus, floating pear tree).
The features are the ones of the type species. Characteristic polyamines are putrescine and spermidine. Major fatty acids are C16:0, C16:1 ω7c and C18:1 ω9c. The G + C content is about 54%.
The type species is Planctopirus limnophilus. Planctopirus belongs to Planctomycetaceae.
Description of Planctopirus limnophilus(Hirsch and Müller 1986) comb. nov.
Planctopirus limnophilus (lim.no’phi.la Gr. n. limnos lake; Gr. adj. philus loving; NL adj. limnophila lake loving).
Basonym: Planctomyces limnophilus Hirsch and Müller 1986.
The genus Planctopirus is comprised of one species, Planctopirus limnophilus. The characteristics of the species are given in the genus description and the description given by Hirsch and Müller (1986) .
The type strain is Mü 290T (=ATCC 43296 = DSM 3776 = IFAM 1008).
Description of Gimesia gen. nov.
Gimesia (Gi.me’si.a N. L. fem. n. Gimesia named in honor of Nándor István Gimesi, a Hungarian plant physiologist and plant morphologist, who first reported organisms now placed in the phylum Planctomycetes).
The features are the ones of the type species. The only major polyamine component is sym-homospermidine. The polar lipids contain phosphatidyl-monomethylethanolamine and phosphatidyl-dimethylethanolamine. Major fatty acids are C16:0 and C16:1 ω7c. The G + C content is about 50%.
The type species is Gimesia maris. Gimesia belongs to Planctomycetaceae.
Description of Gimesia maris(ex Bauld and Staley 1976) comb. nov.
Gimesia maris (mar’is L. gen. noun maris of the sea).
Basonym: Planctomyces maris (ex Bauld and Staley 1976) Bauld and Staley 1980.
The genus Gimesia is comprised of one species Gimesia maris. The characteristics of the species are given in the genus description and the description given by Bauld and Staley (1976)  and Bauld and Staley (1980) .
The type strain is 534-30T (=ATCC 29201 = DSM 8797).
This study presents the genome sequence for the P. brasiliensis type strain IFAM 1448T, whose physiological and genomic features are reviewed in detail. Results from phylogenomic analyses including all available Planctomycetaceae genomes disagree with the present circumscription of the genera Planctomyces and Schlesneria. The revisited 16S rRNA gene and phenotypic data from the literature neither support the current classification. A quantitative comparison of phylogenetic and phenotypic aspects suggest the formation of three new genera (for which we propose the names Gimesia, Planctopirus and Rubinisphaera) to accommodate P. maris, P. limnophilus and P. brasiliensis, respectively. Considerable differences between the reported G + C content of Gemmata obscuriglobus, Singulisphaera acidiphila and Zavarzinella formosa and G + C content calculated from their genome sequences are found, suggesting the emendation of their species descriptions. The range of G + C values reported for the Planctomycetaceae (Planctomycetales) indicate that the descriptions of the family and the order should be emended.
CS, BA and MG conducted the phylogenomic studies. CS, BJT, RM, BA, PH, MG and HPK drafted the manuscript. MR performed the laboratory experiments. ML, MN, AL, JFC, LG, SP, MH, KL, IP, KM, NI, AP, AC, KP, CDJ, LH, ML, JCD, TW, JAE, VM and NCK sequenced, assembled and annotated the genome. All authors read and approved the final manuscript.
We gratefully acknowledge the help of Helga Pomrenke for growing P. brasiliensis cultures and Evelyne-Marie Brambilla for DNA extraction and quality control (both at DSMZ). We are grateful to Erko Stackebrandt and Christian Jogler (both at DSMZ) for hints regarding Planctomycetes classification and to Edina Weidemann for information regarding the biography of N.I. Gimesi. This work was performed under the auspices of the US Department of Energy Office of Science, Biological and Environmental Research Program, and by the University of California, Lawrence Berkeley National Laboratory under contract No. DE-AC02-05CH11231, Lawrence Livermore National Laboratory under Contract No. DE-AC52-07NA27344, and Los Alamos National Laboratory under contract No. DE-AC02-06NA25396, UT-Battelle and Oak Ridge National Laboratory under contract DE-AC05-00OR22725, as well as German Research Foundation (DFG) INST 599/1-2.
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