Description of a Novel Actinobacterium Microbacterium assamensis sp. nov., Isolated from Water Sample Collected from the River Brahmaputra, Assam, India

A Gram-positive, yellow pigmented actinobacterium, strain S2-48(T) was isolated from water sample collected from the river Brahmaputra, Assam, India and subjected to a polyphasic taxonomic study. Most of the physiological and biochemical properties, major fatty acids (C(15:0) Anteiso, iso C(16:0) and C(17:0) Anteiso), estimated DNA G+C content (70.2 mol%) and 16S rRNA gene sequence analysis showed that strain S2-48(T) belonged to the genus Microbacterium. Strain S2-48(T) exhibited highest 16S rRNA gene sequence similarity with Microbacterium testaceum (97.0%); however, the DNA-DNA relatedness value between strain S2-48(T) and M. testaceum was 9.1%. On the basis of differential phenotypic characteristics and genotypic distinctiveness, strain S2-48(T) should be classified within the genus Microbacterium as a novel species, for which the name Microbacterium assamensis is proposed. The type strain is S2-48(T) (=MTCC 10486(T) = DSM 23998(T)).     

Murdannia nampyana (Commelinaceae) sp. nov. from Kerala,India

Murdannia nampyana sp. nov. (Commelinaceae), collected from a marshy riparian area by the Kadambrayar River, near Bhramapuram Diesel Power Project, Kakkanad, Ernakulam district, Kerala is described. The new species can be distinguished from the similar species M. spirata G.Brückn. by its creeping habit, up to 1.5 m long with no definite base (vs erect, ascending, decumbent habit, with or without definite base), 1.1–2.2 cm wide flower diameter (vs 0.65–0.80 cm), petals 1.1 × 0.5–0.7 cm (vs 0.35–0.40 × 0.25–0.35 cm), 0.6–0.5–0.9 cm long stamen filaments (vs 0.06–0.15 cm), 0.20–0.25 cm long staminode filaments, (vs 0.06–0.15 cm), 2–3 smooth seeds per locule, with ridges and furrows and 1–2 small ventral depression on both side of the linear hilum and dorsal embryotega (vs 3–4 verrucose seeds per locule, with ridges and warts, 1–3 deep ventral pits on both side of elliptic hilum, edges of pits surrounded by warts, brownish powdery material in the testa and semidorsal embryotega).     

Oberonia swaminathanii sp. nov. (Orchidaceae) from Kerala,India

Oberonia swaminathanii, a new species of Orchidaceae from Wayanad district, Kerala, India is described and illustrated. The new species resembles Oberonia balakrishnanii, O. chandrasekharanii and O. seidenfadeniana by its 3‐lobed labellum and 2‐lobuled midlobe; but differs in having brick‐red coloured flowers, triangular labellum disc, and a subglobose column.     

Clausena agasthyamalayana sp. nov. (Rutaceae) from Kerala,India

A new species of Clausena, C. agasthyamalayana is described and illustrated from the southern Western Ghats, Kerala, India. It is similar to C. indica but differs from it being of dwarf habit, and having greenish–black bark, smaller and fewer leaflets, obovate and coriaceous leaves with obtuse or emarginated apex, elliptic and obtuse petals, oblong‐cordate anthers, consistently 4‐locular ovary with 2 ovules in each chamber and ellipsoid fruits.     

Rotala tulunadensis sp. nov. (Lythraceae) from Kerala,India

A new aquatic species of the family Lythraceae (Rotala tulunadensis) collected from the lateritic plateau at Permude, Kerala, India is described and illustrated. It is closely allied to R. pterocalyx A. Raynal, but differs in having larger leaves, calyx tube not stretching laterally to include the capsule, calyx without interjected folds in fruit and larger petals.     

Eriocaulon vandaanamense sp. nov. (Eriocaulaceae) from Kerala,India

Eriocaulon vandaanamense (Eriocaulaceae), a new species from a marshy coastal area in the Alappuzha District, Kerala, India, is described and illustrated. The new species is similar to E. truncatum and resembles it in having vertically elongated seed coat cells, but differs mainly in having pale black hoary floral bracts, 3‐lobed hoary male sepals, linear‐falcate, non‐conduplicate hoary female sepals, and small, smooth, pale brown seeds without seed coat appendages.     

Symplocos parvibracteata sp. nov. (Symplocaceae) from the Western Ghats,Kerala, India

Symplocos parvibracteata sp. nov. (Symplocaceae) from Chemunji Hills, south Western Ghats, Kerala State, India, is described and illustrated. It is most similar to S. wynadensis and S. tenella, a putative synonym of S. wynadensis, but differs in having shorter racemes, shorter bracts and bracteoles that are persistent in flower and caducous in fruit, narrowly ellipsoid flower buds, and fewer stamens per flower. It is also similar to S. sumuntia, from which it differs by its pubescent branchlets, generally more stamens per flower, and a pubescent floral disk, and to S. macrophylla, from which it differs by the combination of 3 to 5 leaf secondary veins on each side of the midvein, 1–2‐cm long inflorescences, and bracts that are persistent in flower, caducous in fruit, and < 1.5 mm long.     

Lepidagathis benojiana sp. nov. (Acanthaceae) from the Western Ghats,Kerala, India

Lepidagathis benojiana, a new species of Lepidagathis, collected from the Idukki district, Kerala, southern Western Ghats, India is described along with photographs. The new species is closely allied to L. chlorostachya Nees. but differs from the latter in its height, length of petiole, position and number of spikes, length of peduncle, length of floral whorls, colour of flower, colour and nature of stamens, nature of fruit and shape of the seed.     

Deinococcus soli sp. nov., a Gamma-Radiation-Resistant Bacterium Isolated from Rice Field Soil

A Gram-negative, non-motile, short rod-shaped bacterial strain, designated N5^T, was isolated from a rice field soil in South Korea. Phylogenetic analysis based on the 16S rRNA gene sequence of the new isolate showed that strain N5^T belongs to the genus Deinococcus, family Deinococcaceae, showing the highest sequence similarity to Deinococcus grandis KACC 11979^T (98.4 %) and Deinococcus daejeonensis KCTC 13751^T (97.5 %). Strain N5^T exhibits resistance to gamma-radiation similar to that of other members of the genus Deinococcus, with a D₁₀ value in excess of 4 kGy. Chemotaxonomic data showed that the most abundant fatty acids are C_16:1 ω7c (25.25 %), C_15:1 ω6c (19.77 %), C_17:1 ω6c (11.87 %), and C_17:0 (9.41 %), and the major polar lipid is an unknown phosphoglycolipid. The predominant respiratory quinone is menaquinone MK-8. The DNA G+C content is 71.4 mol%. Phenotypic, phylogenetic, and chemotaxonomic data support designation of strain N5^T as a novel species of the genus Deinococcus, for which the name Deinococcus soli sp. nov. is proposed. The type strain is N5^T (=KCTC 33153^T = JCM 19176^T).     

Zygotorulaspora cornina sp. nov. and Zygotorulaspora smilacis sp. nov., Two Novel Ascomycetous Yeast Species Isolated from Plant Flowers and Fruits

Three isolates belonging to the ascomycetous genus Zygotorulaspora were obtained from the fruits of Cornus officinalis and Smilax china, and flowers of Dendranthema zawadskii var. latilobum in Gongju-si, Korea. Phylogenetic Analyses of the LSU D1/D2 domain and ITS region sequences supported the recognition of two new species: Zygotorulaspora cornina sp. nov. (type strain NIBRFGC000500475 = KACC93346P^PP) and Zygotorulaspora smilacis sp. nov. (type strain NIBRFGC000500476 = KACC93347P^PP). The two novel species revealed no growth on D-Galactose, unlike the other six species in the genus Zygotorulaspora. They are distinguished from each other by their phylogenetic differences and phenotypic characteristics such as assimilation of xylitol, 5-keto-D-gluconate, and ethanol. All species in the genus Zygotorulaspora including the two novel species have phenotypic traits of genus Zygotorulaspora: asci are persistent, sucrose and raffinose are assimilated, and m-inositol is not required for growth, and they are mainly associated with plants.     

Properties of Desulfovibrio carbinolicus sp. nov. and Other Sulfate-Reducing Bacteria Isolated from an Anaerobic-Purification Plant

Several sulfate-reducing microorganisms were isolated from an anaerobic-purification plant. Four strains were classified as Desulfovibrio desulfuricans, Desulfovibrio sapovorans, Desulfobulbus propionicus, and Desulfovibrio sp. The D. sapovorans strain contained poly-beta-hydroxybutyrate granules and seemed to form extracellular vesicles. A fifth isolate, Desulfovibrio sp. strain EDK82, was a gram-negative, non-spore-forming, nonmotile, curved organism. It was able to oxidize several substrates, including methanol. Sulfate, sulfite, thiosulfate, and sulfur were utilized as electron acceptors. Pyruvate, fumarate, malate, and glycerol could be fermented. Because strain EDK82 could not be ascribed to any of the existing species, a new species, Desulfovibrio carbinolicus, is proposed. The doubling times of the isolates were determined on several substrates. Molecular hydrogen, lactate, propionate, and ethanol yielded the shortest doubling times (3.0 to 6.3 h). Due to the presence of support material in an anaerobic filter system, these species were able to convert sulfate to sulfide very effectively at a hydraulic retention time as short as 0.5 h.     

Purification and Properties of a Novel Enzyme,Maltooligosyl Trehalose Synthase,from Arthrobacter sp. Q36

Arthrobacter sp. Q36 produces a novel enzyme, maltooligosyl trehalose synthase, which catalyzes the conversion of maltooligosaccharide into the non-reducing saccharide, maltooligosyl trehalose (α-maltooligosyl α-D-glucoside) by intramolecular transglycosylation. The enzyme was purified from a cell-free extract to an electrophoretically homogeneous state by successive column chromatography on Sepabeads FP-DA13, DEAE-Sephadex A-50, Ultrogel AcA44, and Butyl-Toyopearl 650M. The enzyme was specific for maltooligosaccharides except maltose, and catalyzed the conversion to form maltooligosyl trehalose. The K_m of the enzyme for maltotetraose, maltopentaose, maltohexaose, and maltoheptaose were 22.9mM, 8.7mM, 1.4mM, and 0.9mM, respectively. The enzyme had a molecular mass of 81,000 by SDS-polyacrylamide gel electrophoresis and a pI of 4.1 by gel isoelectrofocusing. The N-terminal and C-terminal amino acids of the enzyme were methionine and serine, respectively. The enzyme showed the highest activity at pH 7.0 and 40°C, and was stable from pH 6.0 to 9.5 and up to 40°C. The enzyme activity was inhibited by Hg²⁺ and Cu2⁺.     

Magnetospirillum bellicus sp. nov., a Novel Dissimilatory Perchlorate-Reducing Alphaproteobacterium Isolated from a Bioelectrical Reactor

Previously isolated dissimilatory perchlorate-reducing bacteria (DPRB) have been primarily affiliated with the Betaproteobacteria. Enrichments from the cathodic chamber of a bioelectrical reactor (BER) inoculated from creek water in Berkeley, CA, yielded a novel organism most closely related to a previously described strain, WD (99% 16S rRNA gene identity). Strain VDY^T has 96% 16S rRNA gene identity to both Magnetospirillum gryphiswaldense and Magnetospirillum magnetotacticum, and along with strain WD, distinguishes a clade of perchlorate-reducing Magnetospirillum species in the Alphaproteobacteria. In spite of the phylogenetic location of VDY^T, attempted PCR for the key magnetosome formation genes mamI and mamL was negative. Strain VDY^T was motile, non-spore forming, and, in addition to perchlorate, could use oxygen, chlorate, nitrate, nitrite, and nitrous oxide as alternative electron acceptors with acetate as the electron donor. Transient chlorate accumulation occurred during respiration of perchlorate. The organism made use of fermentation end products, such as acetate and ethanol, as carbon sources and electron donors for heterotrophic growth, and in addition, strain VDY^T could grow chemolithotrophically with hydrogen serving as the electron donor. VDY^T contains a copy of the RuBisCo cbbM gene, which was expressed under autotrophic but not heterotrophic conditions. DNA-DNA hybridization with strain WD confirmed VDY^T as a separate species (46.2% identity), and the name Magnetospirillum bellicus sp. nov. (DSM 21662, ATCC BAA-1730) is proposed.Dissimilatory perchlorate-reducing bacteria (DPRB) use perchlorate as a terminal electron acceptor during respiration, reducing it completely to chloride. As a consequence, bioremediation of perchlorate has been identified as the most effective means of treating this harmful contaminant (10), which, due to historically unregulated release into the environment, has become widespread (13, 20, 41). Fortunately, DPRB are ubiquitous and can be readily isolated from a variety of environments (1, 10, 11, 39, 44), and a key gene in the pathway, the chlorite dismutase (cld) gene, has been broadly detected (6). Much has been revealed about the biochemistry and genetics of microbial perchlorate reduction through the study of several model organisms, including Dechloromonas aromatica and Dechloromonas agitata, by a variety of groups (5, 6, 8, 9, 17, 28, 29, 34, 35, 38, 47, 51, 56, 57).Less is known about the variation in physiology between these organisms or the evolution of the perchlorate reduction metabolism, highlighting a need for further isolation and characterization of pure cultures. The lack of congruence between phylogenetic trees of cld and the 16S rRNA gene among tested DPRB suggests that the metabolism may be the result of horizontal gene transfer (6). Given that various elements of the pathway may be mobile, it is not unreasonable to expect that organisms with a wide phylogenetic diversity could acquire the ability to reduce perchlorate. As more varied enrichment conditions are tested (2, 39), sometimes as a result of novel bioreactor development for perchlorate treatment (38, 40, 45), the true phylogenetic diversity of DPRB is becoming apparent, supporting the hypothesis that the metabolism may be widespread within the tree of life, similar to other respiratory processes, such as the reduction of sulfate, Fe(III), and nitrate.Although perchlorate has been primarily regarded as an anthropogenic contaminant, a variety of studies have indicated that perchlorate occurs naturally (29-31, 34), which provides a possible explanation for the selective pressure behind the evolution of perchlorate reduction genes. As more is understood about the chlorine redox cycle on earth, knowledge about the diversity of organisms capable of interacting with the various oxyanions of chlorine is becoming more important. Here, we report the characterization of a unique DPRB in the Alphaproteobacteria. Strain VDY^T was isolated from the surface of a working electrode in an active perchlorate-reducing bioelectrical reactor (BER) that was inoculated with water from Strawberry Creek on the University of California, Berkeley, campus (40). This is only the second described DPRB in the Alphaproteobacteria, the other being the closely related strain WD (26), and these strains compose a unique clade of perchlorate-reducing organisms in the genus Magnetospirillum.     

A Novel Protein-Deamidating Enzyme from Chryseobacterium proteolyticum sp. nov., a Newly Isolated Bacterium from Soil

A novel protein-deamidating enzyme, which has potential for industrial applications, was purified from the culture supernatant of Chryseobacterium proteolyticum strain 9670^T isolated from rice field soil in Tsukuba, Japan. The deamidating activities on carboxybenzoxy (Cbz)-Gln-Gly and caseins and protease activity were produced synchronously by the isolate. Both deamidating activities were eluted as identical peaks separated from several proteases by phenyl-Sepharose chromatography of the culture supernatant. The enzyme catalyzed the deamidation of native caseins with no protease and transglutaminase activities. Phenotypic characterization and DNA analyses of the isolate were performed to determine its taxonomy. Physiological and biochemical characteristics, 16S rRNA gene sequence analysis, and DNA-DNA relatedness data indicated that the isolate should be placed as a new species belonging to the genus Chryseobacterium. The isolate showed no growth on MacConkey agar and produced acid from sucrose. The levels of DNA-DNA relatedness between the isolate and other related strains were less than 17%. The name Chryseobacterium proteolyticum is proposed for the new species; strain 9670 is the type strain (=FERM P-17664).     

Alkalisalibacterium limincola gen. nov., sp. nov., an Alkaliphilic Bacterium Isolated from an Alkaline,Saline Lake of Buryatia in Russia

Microbiology - A gram-stain-negative, aerobic, rod-shaped and motile bacterium, designated Alg18-2.2T, was isolated from a bottom sediment of the highly alkaline-saline lake in Buryatia, Russia....