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Three Gram-stain-negative, aerobic, short rod-shaped and motile strains (FXH3W T , SHGZ20W and SMYT11W T ) were isolated from freshwater environments in China. Comparisons based on the 16S rRNA gene sequences indicated that strains FXH3W T and SHGZ20W showed the highest 16S rRNA gene sequence similarity of about 99.6% to ' Luteimonas cellulosilyticus ' MIC 1.5, and strain SMYT11W T showed the highest 16S rRNA gene sequence similarity of 99.8% to Luteimonas fraxinea D4P002 T , respectively. Observing the phylogenetic trees reconstructed based on the 16S rRNA gene sequences, the species of genera Luteimonas and Lysobacter were not monophyletic and often mixed together. The further reconstructed phylogenomic tree and Genome Taxonomy Database also showed that the species of both genera were polyphyletic, implying that the current taxonomic status of the species of both genera was questionable. The calculated OrthoANIu, digital DNA-DNA hybridization and average amino acid sequence identity (AAI) values supported that strains FXH3W T and SHGZ20W should belong to the same novel species and strain SMYT11W T should also represent an independent novel species. Combining the AAI values and phylogenomic analyses, the species of genera Luteimonas and Lysobacter should be reassigned to 12 genera ( Luteimonas , Lysobacter , Cognatiluteimonas , Noviluteimonas , Pseudoluteimonas , Solilutibacter , Agrilutibacter , Cognatilysobacter , Marilutibacter , Novilysobacter , Montanilutibacter and Aerolutibacter ). The AAI values 69.5-76.0% were also proposed as the Lysobacteraceae -specific thresholds for genus delineation. Strain SMYT11W T should represent a novel species of the genus Luteimonas , for which the name Luteimonas flava sp. nov. (type strains SMYT11W T =GDMCC 1.4275 T =KCTC 8304 T ) is proposed. Strains FXH3W T and SHGZ20W should represent a novel species of a new genus Aquilutibacter rugosus gen. nov., sp. nov. The type strain of the type species is FXH3W T (=GDMCC 1.4096 T =KCTC 8154 T ).

A novel proteobacterial strain designated SYSU H10001 T was isolated from a soil sample collected from plateau meadow in Hongyuan county, Sichuan province, south-western China. The taxonomic position of the strain was investigated using a polyphasic approach. On the basis of 16S rRNA gene sequence similarities and phylogenetic analysis, strain SYSU H10001 T was most closely related to Lysobacter soli KCTC 22011 T (98.6%, sequence similarity) and Lysobacter panacisoli JCM 19212 T (98.2%). The prediction result of secondary metabolites based on genome shown that the strain SYSU H10001 T contained 3 clusters of bacteriocins, 1 cluster of non-ribosomal peptide synthetase, 1 cluster of type 1 polyketide synthase and 1 cluster of arylpolyene. In addition, the major isoprenoid quinone was Q-8 and the major fatty acids were identified as iso-C 15:0 , iso-C 17:0 and Summed feature 9. The polar lipids contained diphosphatidylglycerol, phosphatidylglycerol, phosphatidylethanolamine, and three unidentified phospholipids. The genomic DNA G + C content of strain SYSU H10001 T was 66.5% (genome). On the basis of phenotypic, genotypic and phylogenetic data, strain SYSU H10001 T represents a novel species of the genus Lysobacter, for which the name Lysobacter prati sp. nov. is proposed. The type strain is SYSU H10001 T (= KCTC 72062 T  = CGMCC 1.16662 T ).

Strains of Lysobacter , thought to play vital roles in the environment for their high enzyme production capacity, are ubiquitous in various ecosystems. During an analysis of bacterial diversity in saline soil, a Gram-stain-negative, aerobic, chitin-degrading bacterial strain, designated SJ-36 T , was isolated from saline-alkaline soil sampled at Tumd Right Banner, Inner Mongolia, PR China. Strain SJ-36 T grew at 4-40 °C (optimum, 30 °C), pH 5.0-10.0 (optimum, pH 7.0-8.0) and 0-6 % NaCl (optimum, 1.0 %). Oxidase and catalase activities were positive. A phylogenetic tree based on 16S rRNA gene sequences and the phylogenomic tree both showed that strain SJ-36 T formed a tight clade with Lysobacter maris KMU-14 T (sharing 97.6 % 16S rRNA gene similarity) and Lysobacter aestuarii S2-C T (97.8 %). The major polar lipids of strain SJ-36 T were phosphatidylethanolamine, diphosphatidylglycerol, phosphatidylglycerol, two unidentified lipids and one unidentified phospholipid. The major fatty acids were iso-C 15 : 0 (37.5 %), summed feature 9 (14.0 %; iso-C 17 : 1 ω9 c and/or C 16 : 0 10-methyl) and iso-C 11 : 0 (10.6 %). Q-8 was the predominant ubiquinone. Its genomic DNA G + C content was 66.6 mol%. The average nucleotide identity values of strain SJ-36 T to L. maris KMU-14 T , L. aestuarii S2-C T and other type strains were 81.5, 79.1 and <79.0 %, respectively. The results of physiological, phenotypic and phylogenetic characterizations allowed the discrimination of strain SJ-36 T from its phylogenetic relatives. Lysobacter alkalisoli sp. nov. is therefore proposed with strain SJ-36 T (=CGMCC 1.16756 T =KCTC 43039 T ) as the type strain.

A Gram-stain-negative, aerobic, rod-shaped bacterium, designated strain C8-1 T , was isolated from the rhizosphere soil of Nicotiana tabacum L. collected from Kunming, south-west China. The cells showed oxidase-positive and catalase-positive reactions. Growth was observed at 10-40 °C, at pH 6.0-8.0 and in the presence of up to 1 % (w/v) NaCl, with optimal growth at 30 °C and pH 7.0. The predominant isoprenoid quinone was Q-8. The major fatty acids were identified as iso-C15 : 0, iso-C17 : 0 and iso-C17 : 1ω9c. The cellular polar lipids contained diphosphatidylglycerol, phosphatidylglycerol, phosphatidylethanolamine, phosphatidylmethylethanolamine, five unidentified phospholipids and two unidentified aminophospholipids. The genomic DNA G+C content was 70.7 mol%. Phylogenetic analysis based on 16S rRNA gene sequences showed that strain C8-1 T should be assigned to the genus Lysobacter. 16S rRNA gene sequence similarity analysis showed that strain C8-1 T was closely related to Lysobacter cavernae YIM C01544 T (98.6 %), Lysobacter soli DCY21 T (97.6 %), Lysobacter panacisoli CJ29 T (97.3 %), Lysobacter firmicutimachus PB-6250 T (97.3 %), Lysobacter niastensis GH41-7 T (97.3 %) and Lysobacter gummosus KCTC 12132 T (97.1 %). DNA-DNA hybridization data indicated that the isolate may represent a novel genomic species belonging to the genus Lysobacter. Polyphasic taxonomic characteristics indicated that strain C8-1 T represents a novel species of the genus Lysobacter, for which the name Lysobacter tabacisoli sp. nov. is proposed. The type strain is C8-1 T (=KCTC 62034 T =CGMCC 1.16271 T ) .

A novel aerobic bacterial strain, designated ZS60 T , with long, rod-shaped, Gram-staining-negative, aerobic cells was isolated from the soil in the Tianshan Mountains, Xinjiang, China. Phylogenetic analysis based on its 16S rRNA gene sequence indicated that strain ZS60 T was affiliated with the genus Lysobacter, and was most closely related to Lysobacter daejeonensis GH1-9 T (96.9 %), Lysobacter caeni BUT-8 T (96.8 %) and Lysobacter ruishenii CTN-1 T (96.7 %). The average nucleotide identity values between strain ZS60 T , L. daejeonensis GH1-9 T and L. ruishenii CTN-1 T were 78.14 and 78.39 %, respectively. The DNA-DNA relatedness between strain ZS60 T , L. daejeonensis GH1-9 T and L. caeni BUT-8 T were 44.8 and 39.1 %, respectively. The genomic DNA G+C content of the strain ZS60 T was 67.7 mol% (draft genome sequence), and Q-8 was the predominant ubiquinone. The major cellular fatty acids of strain ZS60 T were iso-C15 : 0 (23.4 %), iso-C17 : 0 (17.2 %) and iso-C17 : 1 ω9c (12.6 %). On the basis of genotypic, phenotypic and biochemical data, strain ZS60 T is considered to represent a novel species of the genus Lysobacter, for which the name Lysobacterpsychrotolerans sp. nov. is proposed. The type strain is ZS60 T (=CGMCC 1.15509 T =NBRC 112614 T ).

A yellow-pigmented, Gram-stain-negative, gliding and rod-shaped bacterial strain, designated zong2l5 T , was isolated from a forest soil sample at Dinghu Mountain, Guangdong Province, PR China. Phylogenetic analysis based on the 16S rRNA gene sequence showed that strain zong2l5 T belongs to the genus Lysobacter, and was most closely related to Lysobacter enzymogenes KCTC 12131 T (97.7 %) and Lysobacter soli KCTC 22011 T (97.6 %). The novel strain showed an average nucleotide identity (ANI) value of 81.5 % and a digital DNA-DNA hybridization (dDDH) value of 25.3 % with L. enzymogenes KCTC 12131 T based on draft genome sequences, followed by L. soli KCTC 22011 T with ANI and dDDH values of 79.4 % and 22.7 %, respectively. The DNA G+C content of strain zong2l5 T based on the whole genome sequence was 69.2 mol%. The major fatty acids were iso-C15 : 0, iso-C17 : 0 and summed feature 9 (iso-C17 : 1ω9c and/or 10-methyl C16 : 0). Strain zong2l5 T contained Q-8 as the major isoprenoid quinone and the major polar lipids were diphosphatidylglycerol, phosphatidylglycerol, phosphatidyl-N-methylethanolamine, phosphatidylethanolamine, three unidentified phospholipids and an unidentified aminolipid. The phenotypic, genotypic and chemotaxonomic anlyses clearly showed that strain zong2l5 T represents a novel species of the genus Lysobacter, for which the name Lysobactersilvisoli sp. nov. is proposed. The type strain is zong2l5 T (=GDMCC 1.1489 T =KCTC 52923 T ).

A Gram-negative and aerobic bacterium, designated YIM 77875(T), was isolated from a geothermal soil sample collected at Rehai National Park, Tengchong, Yunnan Province, south-west China. Bacterial growth occurred from 37 to 65 °C (optimum 50 °C), pH 6.0-8.0 (optimum pH 7.0) and 0-1 % NaCl (w/v). Cells were rod-shaped and colonies were convex, circular, smooth, yellow and non-transparent. Phylogenetic analysis based on the 16S rRNA gene sequence indicated that strain YIM 77875(T) belongs to the genus Lysobacter. The 16S rRNA gene sequence similarity values between strain YIM 77875(T) and other species of the genus Lysobacter were all below 94.7 %. The polar lipids of strain YIM 77875(T) were diphosphatidylglycerol, phosphatidylglycerol, phosphatidylethanolamine and five unknown phospholipids. The predominant respiratory quinone was Q-8 and the G+C content was 68.8 mol%. Major fatty acids were iso-C(16:0), iso-C(15:0) and iso-C(11:0). On the basis of the morphological and chemotaxonomic characteristics, as well as genotypic data, strain YIM 77875(T) represents a novel species, Lysobacter thermophilus sp. nov., in the genus Lysobacter. The type strain is YIM 77875(T) (CCTCC AB 2012064(T) = KCTC 32020(T)).

A Gram-negative, aerobic, motile, rod-shaped, arsenite [As(III)]-resistant bacterium, designated strain ZS79(T), was isolated from subsurface soil of an iron mine in China. Phylogenetic analyses based on 16S rRNA gene sequences revealed that strain ZS79(T) clustered closely with strains of five Lysobacter species, with 96.9, 96.1, 96.0, 95.8 and 95.3% sequence similarities to Lysobacter concretionis Ko07(T), L. daejeonensis GH1-9(T), L. defluvii IMMIB APB-9(T), L. spongiicola KMM 329(T) and L. ruishenii CTN-1(T), respectively. The major cellular fatty acids were iso-C(15:0) (28.6%), iso-C(17:1)ω9c (19.9%), iso-C(16:0) (13.6%), iso-C(11:0) (12.6%) and iso-C(11:0) 3-OH (12.4%). The genomic DNA G+C content was 70.7 mol% and the major respiratory quinone was Q-8. The major polar lipids were diphosphatidylglycerol, phosphatidylethanolamine, phosphatidylglycerol and an unknown phospholipid. On the basis of morphological and physiological/biochemical characteristics, phylogenetic position and chemotaxonomic data, this strain is considered to represent a novel species of the genus Lysobacter, for which the name Lysobacter arseniciresistens sp. nov. is proposed; the type strain is ZS79(T) (=CGMCC 1.10752(T)=KCTC 23365(T)).

Two Gram-reaction-negative, rod-shaped, gliding, yellow-pigmented bacterial strains, designated ZLD-17(T) and ZLD-29(T), were isolated from arid soil samples collected from Xinjiang Province, north-west China, and subjected to analysis using a polyphasic taxonomic approach. Both novel strains required 1.0-2.0 % (w/v) sea salts for optimal growth. Phylogenetic analysis based on 16S rRNA gene sequences indicated that these two strains belong to the genus Lysobacter within the class Gammaproteobacteria. Strain ZLD-17(T) showed highest 16S rRNA gene sequence similarities to Lysobacter capsici KCTC 22007(T) (96.9 %), Lysobacter spongiicola DSM 21749(T) (96.8 %) and Lysobacter koreensis KCTC 12204(T) (96.8 %), whereas strain ZLD-29(T) showed highest sequence similarities to Lysobacter niastensis DSM 18481(T) (96.0 %) and Lysobacter enzymogenes DSM 2043(T) (95.9 %). 16S rRNA gene sequence similarity between ZLD-17(T) and ZLD-29(T) was 96.1 %. The DNA G+C contents of strains ZLD-17(T) and ZLD-29(T) were 67.9 and 68.2 mol%, respectively. The major cellular fatty acids of both strains were summed feature 3 (iso-C₁₅:₀ 2-OH and/or C₁₆:₁ω7c), iso-C₁₇:₁ω9c, iso-C₁₆:₀, C₁₆:₀ and iso-C₁₁:₀ 3-OH; their predominant isoprenoid quinone was Q-8 and their major polar lipids were diphosphatidylglycerol, phosphatidylethanolamine and phosphatidylglycerol. Based on their phenotypic characteristics, phylogenetic position as determined by 16S rRNA gene sequence analysis and chemotaxonomic data, strains ZLD-17(T) ( = CCTCC AB 207174(T)  = KCTC 23076(T)) and ZLD-29(T) ( = CCTCC AB 207175(T) = KCTC 23077(T)) represent two novel species of the genus Lysobacter, for which the names Lysobacter korlensis sp. nov. and Lysobacter bugurensis sp. nov. are proposed, respectively.

An aerobic, Gram-negative bacterial strain, designated CTN-1(T), capable of degrading chlorothalonil was isolated from a long-term chlorothalonil-contaminated soil in China, and was subjected to a polyphasic taxonomic investigation. Strain CTN-1(T) grew at 15-37 °C (optimum 28-30 °C) and at pH 6.0-9.0 (optimum pH 7.0-7.5). The G+C content of the total DNA was 67.1 mol%. Based on 16S rRNA gene sequence analysis, strain CTN-1(T) was related most closely to Lysobacter daejeonensis DSM 17634(T) (97.1  % similarity), L. soli DCY21(T) (95.7  %), L. concretionis Ko07(T) (95.5  %), L. gummosus LMG 8763(T) (95.3 %) and L. niastensis DSM 18481(T) (95.2  %). The novel strain showed less than 95.0 % 16S rRNA gene sequence similarity to the type strains of other Lysobacter species. The major cellular fatty acids of strain CNT-1(T) were iso-C₁₆:₀ (23.0  %), iso-C₁₅:₀ (21.4  %) and iso-C₁₇:₁ω9c (15.3  %). The major isoprenoid quinone was Q-8 (99 %), and the major polar lipids were diphosphatidylglycerol, phosphatidylethanolamine and phosphatidylglycerol. These chemotaxonomic data supported the affiliation of strain CTN-1(T) to the genus Lysobacter. Levels of DNA-DNA relatedness between strain CTN-1(T) and L. daejeonensis DSM 17634(T) were 34.6-36.1  %. Phylogenetic analysis based on 16S rRNA gene sequences, DNA-DNA hybridization data and biochemical and physiological characteristics strongly supported the genotypic and phenotypic differentiation of strain CTN-1(T) from recognized species of the genus Lysobacter. Strain CTN-1(T) is therefore considered to represent a novel species of the genus Lysobacter, for which the name Lysobacter ruishenii sp. nov. is proposed. The type strain is CTN-1(T) (=DSM 22393(T) =CGMCC 1.10136(T)).