Reclassification of a reveromycin-producer and the proposals of Actinacidiphila reveromycinica sp. nov. and Actinacidiphila acidipaludis comb. nov.

Streptomyces sp. SN-593, a reveromycin producer, was previously thought to belong to the genus Streptomyces based on its morphological and chemotaxonomic characteristics. In this paper, we re-considered its taxonomic position according to the current criteria. Phylogenetic analysis using 16S rRNA gene sequences showed that the strain belongs to the genus Actinacidiphila. In multilocus sequence and phylogenomic analyses, the strain SN-593 represented a distinct evolutionary lineage within this genus, and its closest neighbor was A. yanglinensis. Digital DNA-DNA hybridization indicated that the strain shares less than 32% DNA-DNA relatedness with the type strains of closely related species, confirming this strain is a novel genomospecies. According to its phenotypic distinctiveness from the closest neighbor, we propose Actinacidiphila reveromycinica sp. nov. for the strain SN-593T. Additionally, as Streptomyces acidipaludis belonged to the genus Actinacidiphila in these analyses, it should be transferred to the genus, for which Actinacidiphila acidipaludis comb. nov. is proposed.

Phytohabitans aurantiacus sp. nov., an actinomycete isolated from soil.

A novel actinomycete, designated RD004123T, was isolated from a soil sample collected in Hokkaido, Japan, and its taxonomic position was investigated by a polyphasic approach. Phylogenetic analysis based on 16S rRNA gene sequence comparisons revealed that strain RD004123T fell within the cluster of the family Micromonosporaceae but did not form a reliable cluster with any member of the family. The similarity values between strain RD004123T and the type species of 29 genera in the family Micromonosporaceae were 91.7-97.7 %. Meanwhile, phylogenomic analyses indicated that strain RD004123T was closely related to members of the genus Phytohabitans. Strain RD004123T contained both meso-diaminopimelic acid and l-lysine as the diagnostic diamino acids of the peptidoglycan. The predominant isoprenoid quinones were MK-10(H8) and MK-10(H6), and the major fatty acids were anteiso-C17 :  0, iso-C16 :  0, iso-C15 :  0 and C17 :  0. The detected polar lipids were phosphatidylinositol mannosides, phosphatidylinositol, phosphatidylethanolamine and diphosphatidylglycerol. These chemotaxonomic features corresponded to those of the genus Phytohabitans. Meanwhile, the results of genome comparison analyses and phenotypic characterizations distinguished strain RD004123T from the other members of the genus Phytohabitans. Therefore, strain RD004123T should be assigned as representing a novel species of the genus Phytohabitans, for which the name Phytohabitans aurantiacus sp. nov. is proposed. The type strain is RD004123T (=NBRC 114997T=DSM 114330T).

Resolution of housekeeping gene sequences used in MLSA for the genus Streptomyces and reclassification of Streptomyces anthocyanicus and Streptomyces tricolor as heterotypic synonyms of Streptomyces violaceoruber.

Although 16S rRNA gene sequences are conventionally analysed in bacterial systematics, their resolution is not sufficient for species identification. Multilocus sequence analysis (MLSA) is a powerful method for species identification as well as the elucidation of phylogenetic relationships in the genus Streptomyces. Gene sequences of atpD, gyrB, recA, rpoB and trpB are generally used in MLSA for Streptomyces species. This study aims to evaluate the sequence analysis of one gene instead of all five genes to be employed for species identification. The resolution of atpD gene sequences was not necessarily able to distinguish closely related species. In contrast, trpB gene sequence similarities correlated to the MLSA-based evolutionary distances, especially among closely related strains. A pairwise similarity of 97.9 % in trpB gene sequences was proposed as the threshold for species delineation based on the feasibility examined using strain pairs that shared >99.93 % pairwise 16S rRNA gene sequence similarities. Resequencing the five housekeeping genes followed by MLSA suggested that Streptomyces anthocyanicus and Streptomyces tricolor are synonyms of Streptomyces violaceoruber.

Reclassification of Streptomyces costaricanus and Streptomyces phaeogriseichromatogenes as later heterotypic synonyms of Streptomyces murinus.

This study aimed to clarify the taxonomic relationships among Streptomyces costaricanus, Streptomyces graminearus, Streptomyces murinus and Streptomyces phaeogriseichromatogenes. These strains share the same 16S rRNA gene sequence. Multilocus sequence analysis revealed that S. costaricanus, S. murinus and S. phaeogriseichromatogenes belong to the same species, but S. graminearus does not. Digital DNA-DNA relatedness and average nucleotide identity among S. costaricanus, S. murinus and S. phaeogriseichromatogenes were 70.9-74.6% and 96.5-97.0 %, respectively. In addition to the previously reported phenotypic data, the presence of a similar set of secondary metabolite-biosynthetic gene clusters for polyketides and nonribosomal peptides supported the similarity among the three species. Therefore, S. costaricanus and S. phaeogriseichromatogenes should be reclassified as later heterotypic synonyms of S. murinus.

Reclassification of four subspecies in the genus Streptomyces to Streptomyces rubradiris sp. nov., Streptomyces asoensis sp. nov., Streptomyces fructofermentans sp. nov. and Streptomyces ossamyceticus sp. nov.

The genus Streptomyces includes, at the time of writing, eight subspecies with validly published names. Streptomyces thermoviolaceus subsp. apingens NBRC 15459T and Streptomyces lavendulae subsp. grasserius NBRC 13045T show 16S rRNA gene sequence similarities of >99.7% to their parent species Streptomyces thermoviolaceus subsp. thermoviolaceus NBRC 13905T and Streptomyces lavendulae subsp. lavendulae NRRL B-2774T, respectively. In contrast, the type strains of the remaining six subspecies, Streptomyces achromogenes subsp. rubradiris, Streptomyces albosporeus subsp. labilomyceticus , Streptomyces cacaoi subsp. asoensis , Streptomyces chrysomallus subsp. fumigatus , Streptomyces cinereoruber subsp. fructofermentans and Streptomyces hygroscopicus subsp. ossamyceticus, do not show >99.0% 16S rRNA gene sequence similarity to that of each parent species. Although S. chrysomallus subsp. fumigatus and S. hygroscopicus subsp. ossamyceticus were respectively reclassified to 'Kitasatospora fumigata' and 'Streptomyces ossamyceticus', these names have not been validly published yet. In this study, we investigated the taxonomic positions of S. achromogenes subsp. rubradiris, S. cacaoi subsp. asoensis, S. cinereoruber subsp. fructofermentans, S. hygroscopicus subsp. ossamyceticus and S. thermoviolaceus subsp. apingens given that their whole genome sequences are available. Except for S. thermoviolaceus subsp. apingens, these subspecies were discriminated from the parent and closely related species based on phylogenetic, genomic and phenotypic differences. Thus, we reclassify S. achromogenes subsp. rubradiris, S. cacaoi subsp. asoensis , S. cinereoruber subsp. fructofermentans and S. hygroscopicus subsp. ossamyceticus as Streptomyces rubradiris sp. nov., Streptomyces asoensis sp. nov., Streptomyces fructofermentans sp. nov. and Streptomyces ossamyceticus sp. nov., respectively. Multilocus sequence and 16S rRNA gene sequence analyses suggested that S. albosporeus subsp. labilomyceticus and S. lavendulae subsp. grasserius may also be reclassified as independent species.

Reclassification of Streptomyces cinnamonensis as a later heterotypic synonym of Streptomyces virginiae.

We studied the taxonomic relationship between Streptomyces cinnamonensis and Streptomyces virginiae. These type strains shared the same 16S rRNA gene sequence. Phylogenomic analysis supported them being closely related. Digital DNA-DNA relatedness and average nucleotide identity using whole genome sequences indicated that the two species represent the same genomospecies. They shared similar phenotypic characteristics and harboured the same set of secondary metabolite-biosynthetic gene clusters for polyketides and nonribosomal peptides in the genomes. Therefore, according to Rule 24b of the Bacteriological Code, S. cinnamonensis Okami 1952, 572AL (Approved Lists 1980) should be reclassified as a later heterotypic synonym of S. virginiae Grundy et al. 1952, 399AL (Approved Lists 1980) emend. Nouioui et al. 2018. Although 16S rRNA gene sequences were identical among type strains of Streptomyces xanthophaeus, Streptomyces spororaveus and Streptomyces nojiriensis and between those of Streptomyces vinaceus and Streptomyces cirratus, respectively, digital DNA-DNA relatedness indicated that these species are not synonymous.

Isolation and structure determination of new linear azole-containing peptides spongiicolazolicins A and B from Streptomyces sp. CWH03.

Linear azole-containing peptides are a class of ribosomally synthesized and post-translationally modified peptides. We performed a chemical investigation on marine actinomycetes, and new linear azole-containing peptides named spongiicolazolicins A and B were found in the MeOH extracts of a newly isolated strain Streptomyces sp. CWH03 (NBRC 114659) and two strains of S. spongiicola (strain HNM0071T: DSM 103383T and strain 531S: NBRC 113560). The strain Streptomyces sp. CWH03 was indicated to be a new species closely related to S. spongiicola by phylogenetic analysis using the genome sequence. The new peptides named spongiicolazolicins A and B were isolated from the cell of Streptomyces sp. CWH03. The partial structure of spongiicolazolicin A was determined by 2D NMR experiments. Based on data of MS/MS experiments, the chemical structures of spongiicolazolicins A and B were proposed using the amino acid sequence deduced from the precursor-encoding gene, which was found from whole-genome sequence data of Streptomyces sp. CWH03. The biosynthetic gene cluster of spongiicolazolicins was proposed based on comparative analysis with that of a known linear azole peptide goadsporin. KEY POINTS: • Streptomyces sp. CWH03 was a new species isolated from marine sediment. • New linear azole-containing peptides named spongiicolazolicins A and B were isolated. • Biosynthetic pathway of spongiicolazolicins was proposed.

Unsaturated fatty acids and a prenylated tryptophan derivative from a rare actinomycete of the genus Couchioplanes.

A genome mining survey combined with metabolome analysis of publicly available strains identified Couchioplanes sp. RD010705, a strain belonging to an underexplored genus of rare actinomycetes, as a producer of new metabolites. HPLC-DAD-guided fractionation of its fermentation extracts resulted in the isolation of five new methyl-branched unsaturated fatty acids, (2E,4E)-2,4-dimethyl-2,4-octadienoic acid (1), (2E,4E)-2,4,7-trimethyl-2,4-octadienoic acid (2), (R)-(-)-phialomustin B (3), (2E,4E)-7-hydroxy-2,4-dimethyl-2,4-octadienoic acid (4), (2E,4E)-7-hydroxy-2,4,7-trimethyl-2,4-octadienoic acid (5), and one prenylated tryptophan derivative, 6-(3,3-dimethylallyl)-N-acetyl-ʟ-tryptophan (6). The enantiomer ratio of 4 was determined to be approximately S/R = 56:44 by a recursive application of Trost's chiral anisotropy analysis and chiral HPLC analysis of its methyl ester. Compounds 1-5 were weakly inhibitory against Kocuria rhizophila at MIC 100 µg/mL and none were cytotoxic against P388 at the same concentration.

Reclassification of Streptomyces diastaticus subsp. ardesiacus, Streptomyces gougerotii and Streptomyces rutgersensis.

We investigated the taxonomic relationships among Streptomyces diastaticus subsp. ardesiacus, Streptomyces diastaticus subsp. diastaticus, Streptomyces gougerotii and Streptomyces rutgersensis. The 16S rRNA gene sequence similarity between S. diastaticus subsp. ardesiacus and S. diastaticus subsp. diastaticus was 97.7 %, whereas S. diastaticus subsp. diastaticus, S. gougerotii and S. rutgersensis showed 100 % nucleotide sequence identity. In addition, S. diastaticus subsp. diastaticus, S. gougerotii and S. rutgersensis formed a single clade in the phylogenetic tree. Digital DNA-DNA relatedness between S. diastaticus subsp. diastaticus and S. diastaticus subsp. ardesiacus was only 22.8%, indicative of different species. In comparison, DNA-DNA relatedness values for S. diastaticus subsp. diastaticus, S. gougerotii and S. rutgersensis ranged from 95.8 to 97.2 %, suggesting the three taxa belong to the same genomospecies. Previously reported phenotypic data also supported synonymy. Therefore, we propose that S. diastaticus subsp. ardesiacus should be classified as an independent species, Streptomyces ardesiacus sp. nov. The type strain is NBRC 13412T (=ATCC 3315T=CBS 713.72T=DSM 40496T=ISP 5496T=JCM 4745T=NBRC 3714T=NRRL B-1241T=RIA 1373T). Our data also suggests that S. rutgersensis and S. gougerotii should be reclassified as later heterotypic synonyms of S. diastaticus.

Reclassification of Streptomyces fulvissimus as a later heterotypic synonym of Streptomyces microflavus.

We investigated the taxonomic relationships among Streptomyces fulvissimus, Streptomyces fulvorobeus and Streptomyces microflavus. These type strains shared the same 16S rRNA gene sequence. Digital DNA-DNA relatedness and average nucleotide identity analyses using whole genome sequences suggested that S. fulvissimus and S. microflavus belong to the same genomospecies, whereas S. fulvorobeus does not. In addition to previously reported phenotypic data, the presence of almost the same set of secondary metabolite-biosynthetic gene clusters for polyketides and nonribosomal peptides also supported the synonymy between S. fulvissimus and S. microflavus. Therefore, S. fulvissimus should be reclassified as a later heterotypic synonym of S. microflavus.

Reclassification of Streptomyces hygroscopicus subsp. glebosus and Streptomyces libani subsp. rufus as later heterotypic synonyms of Streptomyces platensis.

We investigated the taxonomic relationships among Streptomyces hygroscopicus subsp. glebosus, Streptomyces libani subsp. rufus and Streptomyces platensis. The three species formed a single clade in the phylogenetic trees based on 16S rRNA gene sequence and multilocus sequence analyses. Digital DNA-DNA hybridization using whole genome sequences suggested that S. hygroscopicus subsp. glebosus, S. libani subsp. rufus and S. platensis belong to the same genomospecies. Previously reported phenotypic data also supported this synonymy. Therefore, S. hygroscopicus subsp. glebosus and S. libani subsp. rufus should be reclassified as later heterotypic synonyms of S. platensis.

Reclassification of Streptomyces castelarensis and Streptomyces sporoclivatus as later heterotypic synonyms of Streptomyces antimycoticus.

We investigated the taxonomic relationship between Streptomyces antimycoticus, Streptomyces castelarensis, Streptomyces sporoclivatus, and Streptomyces violaceusniger. Digital DNA-DNA hybridisation using whole genome sequences and multilocus sequence analysis indicated that S. antimycoticus, S. castelarensis, and S. sporoclivatus belong to the same genomospecies. Previously reported phenotypic data also supported this synonymy. Therefore, S. castelarensis and S. sporoclivatus should be reclassified as later heterotypic synonyms of S. antimycoticus. The type strain of S. antimycoticus is NBRC 12839T (=ATCC 23880T=CBS 660.68T=RIA 1198T=CGMCC 4.1591T=DSM 40284T=JCM 4228T=JCM 4621T=KCTC 9694T=NRRL 2421T=NRRL ISP-5284T=VKM Ac-1824T). This study also revealed that genome sequence-published S. violaceusniger NRRL F-8817 should be reclassified into S. antimycoticus.

Classification of 'Streptomyces hyalinum' Hamada and Yokoyama as Embleya hyalina sp. nov., the second species in the genus Embleya, and emendation of the genus Embleya.

The 16S rRNA gene sequence of 'Streptomyces hyalinum' NBRC 13850T shows 99.7 % similarity to that of Embleya scabrispora DSM 41855T; however, it shows <96.1 % similarity to any other type strains, including Streptomyces spp. Phylogenetic analysis based on 16S rRNA gene sequences clearly suggests that 'S. hyalinum' belongs to the genus Embleya rather than to Streptomyces. The strain possesses ll-diaminopimelic acid in the cell wall. The major menaquinone observed is MK-9(H6), and MK-9(H4) and MK-9(H8) are minor components. The major polar lipids are diphosphatidylglycerol, phosphatidylethanolamine and phosphatidylinositol. In this study, the whole genome of strain NBRC 13850T was sequenced, and digital DNA-DNA hybridisation between 'S. hyalinum' NBRC 13850T and E. scabrispora DSM 41855T demonstrated 31.2 % of relatedness value between the two genomes. Morphological, chemotaxonomic, biochemical and physiological data also revealed that 'S. hyalinum' can be easily differentiated from E. scabrispora (the only the valid species of the genus Embleya) and that it merits separate species status. This phenotypic and genetic evidence reveals that 'S. hyalinum' represents a novel species of the genus Embleya; the name Embleya hyalina sp. nov. is proposed for this species. The type strain is NBRC 13850T (=ATCC 29817T=MB 891-A1T). We also emended the description of the genus Embleya considering the feature of E. hyalina.

A cyclopeptide and three oligomycin-class polyketides produced by an underexplored actinomycete of the genus Pseudosporangium.

Aside from the well-studied conventional actinomycetes such as Streptomyces, the less investigated genera of actinomycetes also represent a promising source of natural products. Genome mining indicated that members of the underexplored genus Pseudosporangium, from which no secondary metabolites have been reported to date, may harbor the biosynthetic machinery for the formation of novel natural products. The strain RD062863, that is available at a public culture collection, was obtained and subjected to metabolite analysis, which resulted in the discovery of a novel cyclopeptide, pseudosporamide (1), along with three new oligomycin-class polyketides, pseudosporamicins A-C (2-4). The unusual structure of compound 1, featured by a biaryl-bond bridging across a tripeptide scaffold, N-acetyl-ʟ-Tyr-ʟ-Pro-ʟ-Trp, was determined by a combination of spectroscopic analyses, chemical derivatization, ECD calculation, and DFT-based theoretical chemical shift calculation, revealing the presence of an (S a)-axial chirality around the biaryl bond. Compounds 2-4 lacked hydroxylation on the side chain of the spiroacetal rings, which showed clear contrast to other oligomycin congeners and related polyketides with ring-truncation or expansion. The new macrolides 2-4 displayed potent antimicrobial activity against the Gram-positive bacterium Kocuria rhizohpila and the plant pathogenic fungus Glomerella cingulata. All compounds showed moderate cytotoxicity against P388 murine leukemia cells with IC50 values in the micromolar to submicromolar ranges. These results exemplified the validity of phylogeny-focused strain selection combined with biosynthetic gene-directed genome mining for the efficient discovery of new natural products.

Reclassification of 15 Streptomyces species as synonyms of Streptomyces albogriseolus, Streptomyces althioticus, Streptomyces anthocyanicus, Streptomyces calvus, Streptomyces griseoincarnatus, Streptomyces mutabilis, Streptomyces pilosus or Streptomyces rochei.

Taxonomic relationships in eight sets of Streptomyces species, (1a) Streptomyces enissocaesilis, Streptomyces plicatus, Streptomyces rochei and Streptomyces vinaceusdrappus, (1b) Streptomyces geysiriensis, (2) Streptomyces luteus and Streptomyces mutabilis, (3) Streptomyces flavoviridis and Streptomyces pilosus, (4) Streptomyces asterosporus and Streptomyces calvus, (5) Streptomyces erythrogriseus, Streptomyces griseoincarnatus, Streptomyces labedae and Streptomyces variabilis, (6a) Streptomyces griseorubens, (6b) Streptomyces matensis, (6c) Streptomyces althioticus, (7) Streptomyces albogriseolus and Streptomyces viridodiastaticus, (8a) Streptomyces humiferus and Streptomyces violaceolatus, (8b) Streptomyces anthocyanicus, Streptomyces coelescens and Streptomyces violaceoruber, were investigated. Type strains within each subset of 1a to 8b shared completely identical 16S rRNA gene sequences. In MLSA, subsets 1a and 1b, 6a to 6c, and 8a and 8b formed an independent clade, respectively, but the evolutionary distances between S. violaceoruber and the other members in set 8 and between S. griseorubens and those in set 6 were 0.022-0.023 and 0.0064-0.0076, respectively. Members in each of the other sets, except for S. labedae, formed an independent clade. In each clade, evolutionary distances between/among the members were <0.007 except for that between S. griseorubens and S. matensis in set 6, suggesting the same species. Digital DNA-DNA relatedness using whole genome sequences and phenotypic similarities supported the synonymies of sets 1 to 3, set 4 except for S. labedae, sets 5 to 7, and set 8 except for S. violaceoruber, respectively. Therefore, S. enissocaesilis, S. geysiriensis, S. plicatus and S. vinaceusdrappus were considered as later heterotypic synonyms of S. rochei; S. luteus as that of S. mutabilis; S. flavoviridis as that of S. pilosus; S. asterosporus as that of S. calvus; S. erythrogriseus and S. variabilis as those of S. griseoincarnatus; S. griseorubens and S. matensis as that of S. althioticus; S. viridodiastaticus as that of S. albogriseolus; S. coelescens, S. humiferus and S. violaceolatus as those of S. anthocyanicus.

Transfer of Streptomyces catbensis Sakiyama et al. 2014 and Streptomyces seranimatus Wang et al. 2012 to Yinghuangia catbensis comb. nov. and Yinghuangia seranimata comb. nov.

Phylogenetic analysis of Streptomyces catbensis VN07A0015T and Streptomyces seranimatus YIM 45720T based on 16S rRNA gene sequences suggested that these two strains are related to the genus Yinghuangia rather than Streptomyces. The strains form smooth spores in their spore chains and possessed ll-diaminopimelic acid in cell walls. Their main whole-cell sugars are arabinose, glucose, rhamnose and ribose, or ribose, mannose and galactose, respectively. The menaquinones are MK-9(H8), MK-9(H6) and MK-9(H4). The major polar lipids contain phosphatidylethanolamine, diphosphatidylglycerol and phosphatidylinositol. These characteristics are consistent with the description of the genus Yinghuangia. Physiological, biochemical and chemotaxonomic data clarified that these two strains can be differentiated each other and also from Yinghuangia. aomiensis, only the valid species of the genus Yinghuangia. Therefore, S. catbensis Sakiyama et al. 2014 and S. seranimatus Wang et al. 2012 should be transferred to the genus Yinghuangia and be affiliated to different species, for which the names Yinghuangia catbensis comb. nov. (type strain VN07A0015T=NBRC 107860T=VTCC-A-1889T=VTCC 41889T) and Yinghuangia seranimata comb. nov. (type strain YIM 45720T=CCTCC AA 206006T=DSM 41883T=BCRC 16903T) are proposed.

Reclassification of Streptomyces rimosus subsp. paromomycinus as Streptomyces paromomycinus sp. nov.

Streptomyces rimosus is currently composed of two subspecies: Streptomyces rimosus subsp. rimosus and Streptomyces rimosus subsp. paromomycinus. The 16S rRNA gene similarity between type strains of these two subspecies is 99.03 %, whereas that between S. rimosus subsp. paromomycinus and Streptomyces chrestomyceticusis 100 %. To assess the taxonomic status of S. rimosus subsp. paromomycinus, genome sequencing was performed on the type strains of S. rimosus subsp. paromomycinus and S. chrestomyceticus. Digital DNA-DNA hybridization values between S. rimosus subsp. paromomycinus NBRC 15454T and S. rimosus subsp. rimosus ATCC 10970T and between S. rimosus subsp. paromomycinus NBRC 15454T and S. chrestomyceticus NBRC 13444T were 35.4 and 59.9 %, respectively, which are less than the thresholds for bacterial species delineation and indicate that S. rimosus subsp. paromomycinus is not S. rimosus, but an independent species different from S. rimosus and S. chrestomyceticus. In addition, phenotypic data also support that S. rimosus subsp. paromomycinus is distinct from S. chrestomyceticus. Therefore, S. rimosus subsp. paromomycinus should be reclassified as a novel species, for which we propose the name Streptomyces paromomycinus sp. nov. The type strain is NBRC 15454T (=ATCC 14827T=DSM 41429T=JCM 4541T=JCM 4871T=NRRL 2455T=VKM Ac-605T).

Isolation and structure determination of a new lasso peptide specialicin based on genome mining.

Based on genome mining, a new lasso peptide specialicin was isolated from the extract of Streptomyces specialis. The structure of specialicin was established by ESI-MS and NMR analyses to be a lasso peptide with the length of 21 amino acids, containing an isopeptide bond and two disulfide bonds in the molecule. The stereochemistries of the constituent amino acids except for Trp were determined to be L and the stereochemistry of Trp at C-terminus was determined to be D. Three dimensional structure of specialicin was determined based on NOE experimental data, which indicated that specialicin possessed the similar conformational structure with siamycin I. Specialicin showed the antibacterial activity against Micrococcus luteus and the moderate anti-HIV activity against HIV-1 NL4-3. The biosynthetic gene cluster of specialicin was proposed from the genome sequence data of S. specialis.

Linfuranones B and C, Furanone-Containing Polyketides from a Plant-Associated Sphaerimonospora mesophila.

Two new furanone-containing polyketides, linfuranones B and C, were isolated from a plant-associated actinomycete of the genus Sphaerimonospora. Their structures were determined by NMR and MS spectroscopic analyses, and the absolute configurations were established by anisotropic methods and chemical degradation approaches. In silico analysis of biosynthetic genes suggested that linfuranone B is generated from linfuranone C by oxidative cleavage of the polyketide chain. Linfuranones B and C induced preadipocyte differentiation into matured adipocytes at 20-40 µM without showing cytotoxicity.

Genome analysis-based reclassification of Streptomyces endus and Streptomyces sporocinereus as later heterotypic synonyms of Streptomyces hygroscopicus subsp. hygroscopicus.

The aim of this study was to reclarify the taxonomic relationship among Streptomyces hygroscopicus subsp. hygroscopicus, Streptomyces endus and Streptomyces sporocinereus. Whole genome shotgun sequencing was performed for the type strains of these three taxa. Average nucleotide identity and digital DNA-DNA hybridization values among the three taxa were greater than the thresholds for bacterial species delineation, indicating that they belong to the same genomospecies. In addition, the phenotypic data previously reported also support the synonymy. Therefore, S. endus and S. sporocinereus should be reclassified as later heterotypic synonyms of S. hygroscopicus subsp. hygroscopicus.