Antibacterial activity of Metal nanoparticles produced by Streptomyces spp. Isolated from soil samples

Twenty-five soil samples were collected from Hilla city. (10) Actinomyctes isolates were isolated. Five Streptomyces spp. Late was diagnosed. Isolates positive for a gram and having grey Aerial Mycelium and yellow-green Substrate mycelium on yeast-malt extract medium. All Streptomyces spp. olates d for nanoparticles production. Streptomyces spp.2 was able for producing of omyces spp.2 was, grey aerial, yellow-green substrate mycelium, unable for in producing, having the ability for using glucose, sucrose, mannitol, negative for fructose and mannose, negative for indole, and vogas Proskauer, positive for methyl red test and citrate utilization, negative for catalase and urea test. UV spectrum for ZnO particles showed maximum absorption at 418 nm. FT-IR spectrum for ZnO nanoparticles represented absorption peak at 3425.58 cm-1 is O-H group, 2360.87 cm-1 is CΞC , 1678.07 cm-1 is C=O group, 1388.75 cm-1 is C-H group,1089,78 cm-1 is C-O bending, 1006.84 cm-1 is C-O stretching,615.36 cm-1 is C-H, and 545.86 cm-1 is C-cl stretching. SEM shows the ability of Streptomyces spp.2 for spherical ZnO nanoparticles synthesizing with size (78.96) nm. Streptomyces spp.2 ZnO nanoparticles were having a great effect on E.coli, with inhibition zone (20 mm) and (15,18) mm against S.aureus, Klebsiella pneumonia.

Antifungal and antibacterial activities of Streptomyces polymachus sp. nov. isolated from soil

Strain T258T was isolated from forest soil at Bongnae Falls, South Korea. The strain exhibited antimicrobial and antifungal activity against the following strains: Bacillus subtilis, Staphylococcus aureus, Pseudomonas aeruginosa, Paenibacillus larvae, Escherichia coli, Candida albicans and Aspergillus niger. Growth occurred on all ISP media tested (2, 3, 4, 5, 6 and 7), Czapek–Dox agar, potato dextrose agar, trypticase soy agar, Bennett's modified agar and nutrient agar at 28 °C. Aerial spores were produced solely on ISP Medium 4; the colour of the aerial mycelium was white and the substrate mycelium was ivory. Melanin production was negative on peptone–yeast extract iron agar (ISP Medium 6). The cell-wall peptidoglycan contained ll-diaminopimelic acid, glutamic acid, alanine and glycine. Whole-cell hydrolysates contained glucose, ribose and galactose. The predominant menaquinones were MK-9(H6) and MK-9(H8) while the minor menaquinone was MK-10(H2). The polar lipids included diphosphatidylglycerol, phosphatidylethanolamine and phosphatidylinositol. The major fatty acids (>10 %) were C16 : 0 (29.8 %), summed feature 3 (C16 : 1ω7c and/or C16 : 1ω6c) (15.1 %), anteiso-C15 : 0 (13.5 %) and iso-C15 : 0 (10.3 %). DNA–DNA similarity with other strains ranged between 37.84 ± 1.15 % and 50.25 ± 1.91 %. On the basis of these data, we suggest that strain T258T represents a novel species that belong to the genus Streptomyces, for which we propose a name Streptomyces polymachus sp. nov. The type strain is T258T ( = KACC 18247T = KEMB 9005-212T = NBRC 110905T).

Actinophytocola sediminis sp. nov., an actinomycete isolated from a marine sediment

A novel actinomycete strain, designated YIM M13705T, was isolated from a marine sediment sample of the South China Sea and its characteristics were determined by a polyphasic approach. The slowly growing, Gram-stain-positive, aerobic strain produced branched substrate mycelium and aerial hyphae, and no diffusible pigment was produced on the media tested. At maturity, spore chains were formed on aerial hyphae and substrate mycelium was not fragmented. Whole-cell hydrolysates of the strain contained meso-diaminopimelic acid and galactose, glucose, ribose and rhamnose. The predominant menaquinones were MK-9(H4) and MK-10(H2). The polar lipids detected were diphosphatidylglycerol, phosphatidylethanolamine, hydroxyphosphatidylethanolamine, phosphatidylinositol and ninhydrin-positive phosphoglycolipids. The major fatty acid was iso-C16 : 0. The G+C content of the genomic DNA was 68.2 mol%. On the basis of 16S rRNA gene sequence, the strain was shown to be most closely related to species of the genus Actinophytocola . DNA–DNA hybridization relatedness values (<70 %) of the isolate with its closest neighbour Actinophytocola xinjiangensis QAIII60T supported classification of the isolate as a representative of a novel species. On the basis of phylogenetic analysis, and phenotypic and genotypic data, it is concluded that the new isolate belongs to a novel species of the genus Actinophytocola , for which the name Actinophytocola sediminis sp. nov. (type strain YIM M13705T = DSM 45939T = BCRC 16956T) is proposed.

Pseudonocardia sediminis sp. nov., isolated from marine sediment

A Gram-stain-positive, aerobic actinomycete, designated strain YIM M13141T, was isolated from a marine sediment sample from the South China Sea, and its taxonomic position was determined using a polyphasic approach. The strain produced branched substrate mycelium and aerial hyphae, but no diffusible pigments were produced on the media tested. At maturity, substrate mycelium was fragmented and spore chains were formed on aerial hyphae and substrate mycelium. Optimum growth occurred at 28 °C, 1–3 % (w/v) NaCl and pH 7.0. Comparative analysis of the 16S rRNA gene sequence showed that the isolate belongs to the genus Pseudonocardia , showing highest levels of similarity with respect to Pseudonocardia sichuanensis KLBMP 1115T (97.1 %), Pseudonocardia tetrahydrofuranoxydans K1T (97.1 %) and Pseudonocardia kunmingensis YIM 63158T (97.0 %). Whole-organism hydrolysates of the strain contained meso-diaminopimelic acid and the sugars galactose, glucose, mannose and arabinose. The predominant menaquinone was MK-8(H4). The polar lipids detected were diphosphatidylglycerol, phosphatidylcholine, phosphatidylinositol, phosphatidylmethylethanolamine, phosphatidylethanolamine, two unknown phosphoglycolipids and two glycolipids. The major fatty acid was iso-C16 : 0. The G+C content of the genomic DNA was 73.1 mol%. DNA–DNA relatedness with P. tetrahydrofuranoxydans DSM 44239T was 42.8±3.5 % (mean±sd). Based on phylogenetic analysis, phenotypic and genotypic data, it is concluded that the isolate represents a novel species of the genus Pseudonocardia , for which the name Pseudonocardia sediminis sp. nov. is proposed. The type strain is YIM M13141T ( = DSM 45779T = JCM 18540T).

Labedaea rhizosphaerae gen. nov., sp. nov., isolated from rhizosphere soil

A novel actinomycete, designated strain RS-49T, was isolated from the rhizosphere soil of a cliff-associated plant (Peucedanum japonicum Thunb.) in the Republic of Korea and subjected to a polyphasic taxonomic study. The results of comparative 16S rRNA gene sequence analyses showed that the organism belonged to the family Pseudonocardiaceae , suborder Pseudonocardineae and that it was most closely related to members of the genera Kibdelosporangium (96.6–97.0 % sequence similarity), Actinokineospora (96.3–96.7 %), Streptoalloteichus (96.2 %) and Actinophytocola (96.2 %). Substrate mycelia were well-developed and whitish or pale yellow to strong yellow. Aerial mycelia were branched and fragmented into rod-shaped elements. Single spherical spores were produced directly on the substrate mycelium. Sporangium-like structures and fragmentation of the substrate mycelium were absent. The diagnostic diamino acid in the cell-wall peptidoglycan was meso-diaminopimelic acid. The acyl type of the muramic acid residues in the peptidoglycan was N-acetylated. Whole-cell sugars were glucose, rhamnose, galactose, ribose, mannose, arabinose and xylose. The major menaquinone was MK-9(H4). Small amounts of MK-8 and MK-9(H2) were also detected. The polar lipids contained diphosphatidylglycerol, phosphatidyldimethylethanolamine, phosphatidylglycerol, phosphatidylinositol, an unknown phospholipid and an unknown lipid. The predominant fatty acids were iso-C15 : 0 and iso-C16 : 0. The DNA G+C content was 64.2 mol%. The phenotypic and phylogenetic characteristics show that strain RS-49T can be differentiated from members of all genera in the suborder Pseudonocardineae and thus represents a novel species in a new genus for which the name Labedaea rhizosphaerae gen. nov., sp. nov. is proposed; the type strain of the type species is RS-49T ( = KCTC 19662T = DSM 45361T).

Streptomyces fenghuangensis sp. nov., isolated from seawater

An actinomycete, designated strain GIMN4.003T, was isolated from seawater collected in Sanya, China. It produced white aerial mycelium and yellow substrate mycelium on Gause’s synthetic agar medium no. 1. The substrate mycelium colour was not sensitive to pH. Scanning electron microscopy observations revealed that GIMN4.003T produced straight to flexuous spore chains of rough to warty spores. ll-Diaminopimelic acid was present in the cell-wall hydrolysate. Based on chemotaxonomy and morphological features, strain GIMN4.003T was identified as a member of the genus Streptomyces. Melanin was not produced. No antimicrobial activity was detected against Escherichia coli, Pseudomonas aeruginosa, Bacillus subtilis, Penicillium citrinum or Candida albicans. Analysis of the 16S rRNA gene sequence revealed that the highest sequence similarity was to Streptomyces radiopugnans R97T (99.0 %). However, DNA relatedness between GIMN4.003T and S. radiopugnans DSM 41901T was low (41.24±1.47 %). Furthermore, the morphological, physiological and biochemical characteristics of strain GIMN4.003T were different from those of S. radiopugnans DSM 41901T and the type strains of other closely related Streptomyces species. On the basis of its physiological and molecular properties, it is evident that strain GIMN4.003T ( = CCTCCM 208215T = NRRL B-24801T) represents the type strain of a novel species within the genus Streptomyces, for which the name Streptomyces fenghuangensis sp. nov. is proposed.

The interplay of glycogen metabolism and differentiation provides an insight into the developmental biology of Streptomyces coelicolor

Mycelial colonies of the developmentally complex actinomycete Streptomyces coelicolor growing on solid medium contain glycogen in two distinct locations. Phase I deposits are found in a substrate mycelium region bordering the developing aerial mycelium. Their production involves GlgBI, one of two glycogen branching enzyme isoforms. Phase II deposits occur in the upper regions of aerial hyphae, in long tip cells that are dividing, or have just divided, into unigenomic prespore compartments. Their formation involves a second branching enzyme isoform, GlgBII. To find out if the gene for the second isoform, glgBII, is regulated by any of the well-studied whiA, B, G, H or I genes needed for sporulation septation, glgBI or glgBII was disrupted in a set of whi mutants, and the glycogen phenotypes examined by transmission electron microscopy. In the whiG mutants, deposits were found throughout the aerial mycelium and the adjacent region of the substrate mycelium, but the morphology of all the deposits, i.e. whether they were in the form of granules of branched glycogen or large blobs of unbranched glycan, depended solely on GlgBI. In contrast, the whiA, B, H and I mutations had no obvious effect on the pattern of glycogen deposition, or on the spatial specificity of the branching enzyme isoforms (though phase II glycogen deposits were reduced in size and abundance in the whiA and B mutants, and increased in the whiH mutant). These results indicate that glgBII is regulated (directly or indirectly) by whiG, and not by any of the other whi genes tested, and that the aerial hyphae of a whiG mutant are atypical in being physiologically similar to the substrate hyphae from which they emerge. A new role for aerial hyphae is proposed.

Streptomyces africanus sp. nov., a novel streptomycete with blue aerial mycelium

An actinomycete with blue aerial mycelium and yellow substrate mycelium was isolated from a suburban soil sample collected in Cape Town, South Africa and named strain CPJVR-HT. The colour of the substrate mycelium was not sensitive to changes in pH. The organism produced spiny spores in Spirales spore chains. Chemical taxonomy indicated that it is a member of the genus Streptomyces. Strain CPJVR-HT grew at 45 °C and did not produce melanin or any diffusible pigments. It exhibited weak antibacterial activity against a clinical isolate of Enterococcus faecium, but no antibacterial activity against Escherichia coli ATCC 25922 or Pseudomonas aeruginosa ATCC 27853. Analysis of its 16S rRNA gene sequence, DNA–DNA hybridization studies and the results of physiological tests showed that this strain represents a novel species of Streptomyces, for which the name Streptomyces africanus sp. nov. is proposed. The type strain is CPJVR-HT (=NRRL B-24143T=DSM 41829T).