ライフサイエンスコーパス: sp.

1 The two Cpf1 orthologs from Acidaminococcus sp. (AsCpf1) and Lachnospiraceae bacterium (LbCpf1) have

2 re the activity of Cpf1 from Acidaminococcus sp. BV3L6 (As) and Lachnospiraceae bacterium ND2006 (Lb)

3 that two Cpf1 nucleases from Acidaminococcus sp. BV3L6 and Lachnospiraceae bacterium ND2006 (AsCpf1 a

4 ort the crystal structure of Acidaminococcus sp. Cpf1 (AsCpf1) in complex with the guide RNA and its

5 utility of the commonly used Acidaminococcus sp. BV3L6 Cpf1 (AsCpf1) and Lachnospiraceae bacterium ND

6 ved collection of 200 clinical Acinetobacter sp. isolates was tested.

7 ved collection of 200 clinical Acinetobacter sp. Predictive values for susceptibility and resistance

8 al structures of apo-HcaR from Acinetobacter sp. ADP1, a MarR/SlyA transcription factor, in complexes

9 hey were potential human pathogens Aeromonas sp., Stenotrophomonas sp. and an unculturable bacterium.

10 Pressurized liquid extraction of Aglaonema sp. iminosugars has been optimized.

11 perties of curdlan produced by Agrobacterium sp. IFO 13140 and its gels, as well as apply it in food.

12 an and the curdlan produced by Agrobacterium sp. IFO 13140 differed in terms of gelation properties,

13 and reliable quantification of Agrobacterium sp. in samples containing GMO or non GMO samples.

14 probes were designed to target Agrobacterium sp. using the tumor-morphology-shooty gene (TMS1).

15 l possesses three key properties: (i) an all-sp (3) covalent carbon framework that produces high-freq

16 ycobiota showed a predominance of Alternaria sp., Fusarium sp. and Epicoccum sp. Microdochium nivale

17 s, Fusarium brachygibbosum U4 and Alternaria sp. U10, and the specialist herbivore Manduca sexta At l

18 Aminobacter sp. MSH1 uses the groundwater micropollutant 2,6-dichlor

19 t mutant of the BAM mineralizing Aminobacter sp. MSH1 confirmed that 2,6-DCBA produced from BAM is ra

20 Anabaena sp. PCC 7120 is a nitrogen-fixing filamentous cyanobacte

21 Anabaena sp. produces schizokinen and uptake of Fe-schizokinen in

22 ns of Omp85 from the cyanobacterium Anabaena sp. PCC 7120 using pulsed electron-electron double reson

23 erized Prx6 from the cyanobacterium Anabaena sp. strain PCC7120 (AnPrx6) and found that in addition t

24 The closely related cyanobacterium, Anabaena sp. PCC 7120 has the nif1 system but lacks nif2.

25 ched the systems of the filamentous Anabaena sp. PCC 7120 as a model of a siderophore-secreting cyano

26 ion, and function of these genes in Anabaena sp. PCC 7120.

27 is in anaerobic vegetative cells of Anabaena sp. PCC 7120 depended on the presence of cnfR2.

28 d model of the metabolic network of Anabaena sp. PCC 7120 enhances our ability to understand the meta

29 In the model organism Anabaena sp. strain PCC 7120, the septal protein SepJ is required

30 ilm, producing both elastic deformations and sp (2) to sp (3) chemical changes.

31 described as Emarellia grisea gen. nov. and sp. nov; the sixth isolate represents a sister species i

32 ed using a reference Acacia gum (gum arabic, sp. A. senegal) and provided an unambiguous MS profile o

33 40 mum Nylon fibers to brine shrimp (Artemia sp).

34 The dominant fungal genera were Aspergillus sp., Rhizopus sp., Penicillium sp. and Sarocladium sp.,

35 urately identify 133/144 (93.6%) Aspergillus sp. isolates to the species level.

36 r results suggest that TolR enables Azoarcus sp. CIB to adapt to toxic aromatic hydrocarbons under an

37 TCS), from the beta-proteobacterium Azoarcus sp. strain CIB that degrades c-di-GMP in response to aro

38 Bacillus sp. GeD10, a gemfibrozil-degrader, was previously isolat

39 d an As(III)-methylating bacterium, Bacillus sp. CX-1, and identified a gene encoding a S-adenosylmet

40 Overall, gemfibrozil exposure in Bacillus sp. GeD10 increased the abundance of several enzymes pot

41 arsM is constitutively expressed in Bacillus sp. Heterologous expression of BlarsM conferred As(III)

42 The active Mn oxidase in Bacillus sp. PL-12, Mnx, is a complex composed of a multicopper o

43 From the bacterial proteome of Bacillus sp. GeD10 1974 proteins were quantified, of which 284 pr

44 In conclusion, Bacteroidales sp. HOT 274, Desulfobulbus sp. HOT 041, Fretibacterium s

45 ntly higher mean prevalence of Bacteroidales sp. HOT 274, Desulfobulbus sp. HOT 041, Fretibacterium s

46 ficantly higher mean levels of Bacteroidetes sp. human oral taxon (HOT) 274, Fretibacterium sp. HOT 3

47 , viral and parasitic agents like Bartonella sp., Phleboviruses and Leishmania spp., respectively.

48 tZ) and oxyxgenase (CrtW) from Brevundimonas sp. in tomato fruit, followed by beta-carotene enhanceme

49 Here authors synthesize a bulk sp (3)-bonded amorphous form of carbon under high pressu

50 eins of the Prevotella sp. and Butyricimonas sp., another gut commensal.

51 lectrophile coupling is the first to use a C(sp)-X electrophile, and appears to proceed via an alkyny

52 alization protocol for the construction of C(sp)-Si bonds in a single step.

53 Apparently, the C(sp) arylation reaction is the first event on the domino

54 Oxidative addition of the C(sp)-H bond of methyl propiolate along the X-Os-CPh axis

55 Oxidative addition of the C(sp)-H bond of phenylacetylene and methyl propiolate alon

56 nosis of fungal infections caused by Candida sp. yeasts.

57 121, C. cellulans J36 and Cellulosimicrobium sp. strain MM were used to determine distribution of pat

58 Cercozoa sp., Colpoda sp., Protostelium sp. and Vermamoeba sp. ar

59 rom 12 patients and Colpoda steini, Cercozoa sp., Protostelium sp. and a eukaryotic more closely rela

60 Chlamydiae sp. are obligate intracellular pathogens that cause a va

61 conducted with Scenedesmus sp. and Chlorella sp. in the presence and absence of carbonate and in the

62 Metabolomic analyses of Chloroidium sp. UTEX 3007 indicated that the alga accumulates a broa

63 racterized a ubiquitous species, Chloroidium sp. UTEX 3007, which we isolated from multiple locations

64 Bioflocculant synthesis by Citrobacter sp. AzoR-1 using microalga as a substrate, including the

65 be reutilized as a substrate for Citrobacter sp. AzoR-1 cultivation and bioflocculant production.

66 Cercozoa sp., Colpoda sp., Protostelium sp. and Vermamoeba sp. are reported fo

67 tetrahedral amorphous structure and complete sp (3) bonding.

68 patible materials properties to its complete sp (3)-carbon network bonding.

69 Jute (Corchorus sp.) is one of the most important sources of natural fib

70 Seed oils of many Cuphea sp. contain >90% of medium-chain fatty acids, such as de

71 ydra's main bacterial colonizer, Curvibacter sp., responds differentially to N-(3-hydroxydodecanoyl)-

72 ain colonizer, the Gram-negative Curvibacter sp., along the body axis.

73 In contrast, Cyanothece sp. PCC7425 showed neither a preferential accumulation o

74 a) by two cyanobacterial strains, Cyanothece sp. PCC7425 and Gloeomargarita lithophora, both forming

75 of Bacteroidales sp. HOT 274, Desulfobulbus sp. HOT 041, Fretibacterium sp. HOT 360, and Fretibacter

76 on, Bacteroidales sp. HOT 274, Desulfobulbus sp. HOT 041, Fretibacterium sp. HOT 360, Fretibacterium

77 ncrease of Enterobacteriaceae, Desulfovibrio sp., and mainly Akkermansia muciniphila in C-IBS patient

78 The ascidians Diplosoma sp. settled later and were more tolerant to acidificatio

79 ad with WEEV.McM expressing DsRed (Discosoma sp.) and imaged by confocal fluorescence microscopy.

80 reen fluorescent protein (GFP) and Discosoma sp. red fluorescent protein (DsRed) reporter genes drive

81 complete mitochondrial genome of Doedicurus sp., one of the largest glyptodonts.

82 anaviruses and the trematode Echinoparyphium sp.), we examined the influence of coinfection on diseas

83 ex chromosome V of the brown alga Ectocarpus sp. that has a haploid sex determination system (UV syst

84 biting bacterial endophyte, M6 (Enterobacter sp.).

85 a natural bacterial endophyte, Enterobacter sp. strain PDN3, of poplar trees, that rapidly metaboliz

86 le sponge symbiotic bacterium, Entotheonella sp., constitutes the arsenic- and barium-accumulating en

87 Our results indicate that Entotheonella sp. may act as a detoxifying organ for its host.

88 f Alternaria sp., Fusarium sp. and Epicoccum sp. Microdochium nivale (23%), a fungus rarely found in

89 ncultivated intestinal symbiont Epulopiscium sp. type B using fluorescent in situ hybridization.

90 Savannasaurus elliottorum gen. et sp. nov. comprises one of the most complete Cretaceous s

91 scribe Notocolossus gonzalezparejasi gen. et sp. nov. from the Upper Cretaceous of Mendoza Province,

92 atheroidan mammal (Gurbanodelta kara gen. et sp. nov.) discovered at the South Gobi locality in China

93 t the cultivation of Lenisia limosa, gen. et sp. nov., a newly discovered breviate colonized by relat

94 a second species, Gigantotermes rex gen. et sp. nov., based on one of the largest soldier termites y

95 ne described as Krishnatermes yoddha gen. et sp. nov., comprising the worker/pseudergate, winged repr

96 l aleocharine, Mesosymbion compactus gen. et sp. nov., in Burmese amber ( approximately 99 million ye

97 r from Ganzhou, Tongtianlong limosus gen. et sp. nov., represented by a remarkably well-preserved spe

98 uld be concluded that honeys with Eucalyptus sp., Aristotelia chilensis and T.

99 infection structures of Puccinia graminis f. sp. tritici Phylogenetic analysis showed that CBM32s app

100 eat stem rust pathogen, Puccinia graminis f. sp. tritici We present the solution structure of a coile

101 the melon wilt fungus Fusarium oxysporum f. sp. melonis (Fom), bioinformatics-based genome compariso

102 the effector genes of Fusarium oxysporum f. sp. niveum (Fon) races that affect watermelon (Citrullus

103 Alternaria alternata f.sp. Lycopersici (AAL) toxin induces programmed cell deat

104 control activity against Blumeria graminis f.sp. hordei as it parasitizes Hordeum vulgare.

105 hakopsora pachyrhizi and Blumeria graminis f.sp. hordei is compromised in the Arabidopsis cam7 and pe

106 ligate pathogenic fungus Puccinia graminis f.sp. tritici (Pgt), causing the crop disease wheat stem r

107 rum of field isolates of Puccinia graminis f.sp. tritici, including the Ug99 lineage, and are homolog

108 throbacter stackebrantii, and Flavobacterium sp. and the pathogens Vibrio anguillarum and Edwardsiell

109 k anoxic cultures of diatoms (Fragilariopsis sp.) and a chlorophyte (Pyramimonas) isolated from the s

110 4, Desulfobulbus sp. HOT 041, Fretibacterium sp. HOT 360, and Fretibacterium sp. HOT 362 was found in

111 4, Desulfobulbus sp. HOT 041, Fretibacterium sp. HOT 360, Fretibacterium sp. HOT 362, and TM7 sp. HOT

112 . human oral taxon (HOT) 274, Fretibacterium sp. HOT 360, and TM7 sp. HOT 356 phylotypes, as well as

113 , Fretibacterium sp. HOT 360, Fretibacterium sp. HOT 362, and TM7 sp. HOT 356 phylotypes, in addition

114 is (r = 0.51, P = 0.001), and Fretibacterium sp. HOT 360 (r = 0.41) were correlated with pocket depth

115 etibacterium sp. HOT 360, and Fretibacterium sp. HOT 362 was found in subjects with GChP and GAgP tha

116 , strains of F. keratoplasticum and Fusarium sp. FSSC 12 were mostly (25/27) isolated from marine ver

117 orme, Fusarium keratoplasticum, and Fusarium sp. FSSC 12) accounted for four-fifths of the veterinary

118 d a predominance of Alternaria sp., Fusarium sp. and Epicoccum sp. Microdochium nivale (23%), a fungu

119 film was predominantly composed by Geobacter sp. at both experimental conditions.

120 ates following bioaugmentation with Gordonia sp. strain KTR9 (henceforth KTR9) to rates under biostim

121 Halobacterium sp. NRC-1was used to express the N-terminal 199 amino ac

122 roperties, we classify Brachyspira hampsonii sp. nov. as a unique species with genetically diverse ye

123 Helicobacter sp. was detected in 69% of feces or intestinal samples f

124 cted peptide gene products of Herbaspirillum sp. strain RV1423, importing the results of PSAT into EC

125 tudies in the natural producer Herpetosiphon sp. B060.

126 ociated with Triaenops afer and Hipposideros sp. bats that resulted in a NL63-like virus, an ancestor

127 ne S. populator sample and three Homotherium sp. samples, including the only Late Pleistocene Homothe

128 s, with the result that some current Hordeum sp. individuals harbor up to five different panicoid rDN

129 The Jeotgalicoccus sp. peroxygenase cytochrome P450 OleTJE (CYP152L1) is a

130 ures as high as 40 degrees C and Lachlanella sp. 1 at least up to 36 degrees C, but both species show

131 curred above 22 degrees C and in Lachlanella sp. 1 above 15 degrees C.

132 two known heat-tolerant species Lachlanella sp. 1 and Pararotalia calcariformata were collected over

133 h either oral Streptococcus or Lactobacillus sp. bacteria induced a location pattern of neutrophils a

134 re is also a reported increase in Leishmania sp. resistance to these drugs.

135 otential new species, Plasmodium lomamiensis sp. Rare co-infections with non-Laverania parasites were

136 member of this group, Xandarella mauretanica sp. nov., from the middle Cambrian (Stage 5) Tatelt Form

137 s enrichment cultures containing D. mccartyi sp., low C2H2 (0.4 mM) concentrations do not inhibit gro

138 new forstercooperiine, Pappaceras meiomenus sp. nov., from the late Early Eocene Arshanto Formation,

139 ified from Chelativorans (ex. Mesorhizobium) sp. BNC1, its catalytic mechanism is unknown.

140 , Metahaliotrema mizellei and Metahaliotrema sp. (undescribed) were used to develop an automated tech

141 first known virus infecting a Metallosphaera sp., MTIV provides a new system for exploring archaeal v

142 se of the expression level in Methanosarcina sp. was evidenced after oleate addition.

143 ut commensal isolates such as Microbacterium sp., Staphylococcus warneri, Flectobacillus major, Arthr

144 ful blooms of the cyanobacterium Microcystis sp. have become increasingly pervasive in the San Franci

145 quenced isolates known to infect Microcystis sp. was implicated in the bloom's collapse.

146 describe a new species, Gelidium millariana sp. nov., previously identified as G. isabelae from Aust

147 y to those predicted on the basis of the Ms. sp. LW4 Mbn operon.

148 ionship between the endobacterium Mycoavidus sp. and the root-associated fungus Mortierella elongata.

149 between copper toxicity to mussels (Mytilus sp.) and ambient dissolved organic carbon (DOC) concentr

150 ecies, Chinggiskhaania bifurcata n. gen., n. sp., dominates the biota.

151 pecies, Zuunartsphyton delicatum n. gen., n. sp., is known from three specimens.

152 1/3, R. terrestris n. sp. and R. elongata n. sp. and demonstrate that they are related to the coproph

153 ulus 'ithacus' CCAP 1571/3, R. terrestris n. sp. and R. elongata n. sp. and demonstrate that they are

154 ladine 4'-O-methyltransferase from Narcissus sp. and Galanthus spp. was cloned and expressed in Esche

155 sel Bathymodiolus marisindicus, and Neolepas sp. stalked barnacle.

156 how two emerging infectious diseases (Nosema sp. and the Varroa-associated Deformed wing virus (DWV))

157 s H-NOX domains, including those from Nostoc sp. PCC 7120, Shewanella oneidensis, Shewanella woodyi,

158 cyanobacterial T-type lyase CpcT from Nostoc sp. PCC7120 but overall is more compact and smaller.

159 solved two crystal structures of the Nostoc sp. PCC 7120 HCP1 protein, each binding a different caro

160 imetric fossils, Saccorhytus coronarius nov. sp., from an Orsten-like Lagerstatte from the earliest C

161 e of a GFP tagged variant of Novosphingobium sp. LH128 was examined after inoculation into phenanthre

162 species, Ophiothrix fragilis and Ophiothrix sp. II.

163 sts with the panmixia observed in Ophiothrix sp. II across the Atlantic-Mediterranean area.

164 ences (137 of O. fragilis, 215 of Ophiothrix sp. II, and 80 of Ophiothrix sp. III) of the 16S rRNA fr

165 5 of Ophiothrix sp. II, and 80 of Ophiothrix sp. III) of the 16S rRNA from 23 Atlantic-Mediterranean

166 ence of a new congeneric species (Ophiothrix sp. III), occurring in the deep Atlantic coast of the Ib

167 groups of 20 red hybrid tilapia (Orecohromis sp.).

168 lus, for which the name Bacillus oryziterrae sp. nov. is proposed.

169 rmed by a marine-derived fungus Paecilomyces sp. to yield seco-cyclines A-H (9-14, 18 and 19) and hem

170 o isolate a Firmicutes strain (Paenibacillus sp.).

171 eal the intrinsic resistome of Paenibacillus sp. LC231, a cave bacterial isolate that is resistant to

172 peration of home aquaria containing Palythoa sp. soft corals.

173 A single copy of a Panicum sp. rDNA unit present in H. bogdanii had been interrupte

174 ns of the Prevotella sp. and Parabacteroides sp., whereas the HLA-DR-presented FLNA peptide has homol

175 fat diet induces reduction of Parasutterella sp. in the gut, which is significantly correlated with M

176 e Aspergillus sp., Rhizopus sp., Penicillium sp. and Sarocladium sp., occurring at 37, 18, 13 and 12%

177 the obligate relationship between Perkinsela sp. and its amoeba host, and provide a foundation for un

178 Genomic analyses show that Perkinsela sp. has lost the ability to make a flagellum but retains

179 al marine sediment-derived fungus, Phomopsis sp. (CMB-M0042F), yielded the known cytochalasins J (1)

180 d from extracts of the marine sponge Phorbas sp. collected in Howe Sound British Columbia, and their

181 ltured cells of the marine diatom Pinnularia sp. and functionalized with a single chain variable frag

182 dae larvae), 107 +/- 4.5 (pea clams Pisidium sp.), 131 +/- 105 (three-spined sticklebacks: Gasteroste

183 (autoinducer degrading gene from Planococcus sp.).

184 This assay reliably detected Plasmodium sp. parasites in a simple low-tech format, providing a m

185 ninogenica, Prevotella copri, and Prevotella sp. C561 and decreases in Bacteroides spp.

186 ith epitopes from proteins of the Prevotella sp. and Butyricimonas sp., another gut commensal.

187 es from sulfatase proteins of the Prevotella sp. and Parabacteroides sp., whereas the HLA-DR-presente

188 d Colpoda steini, Cercozoa sp., Protostelium sp. and a eukaryotic more closely related to Vermamoeba

189 Cercozoa sp., Colpoda sp., Protostelium sp. and Vermamoeba sp. are reported for the first time a

190 coli used deuterated glucose and Pseudomonas sp. used deuterated naphthalene as sole carbon sources.

191 NA gene Illumina libraries, four Pseudomonas sp. operational taxonomic units surprisingly accounted f

192 in phenylalanine deuteration in Pseudomonas sp. compared to that in E. coli is due to the dilution e

193 l wastewater microorganisms like Pseudomonas sp. were chosen for in-silico screening toward polyester

194 reatly different microorganisms: Pseudomonas sp. NCIB 9816 and Synechococcus elongatus PCC 7942 were

195 was identified in the genome of Pseudomonas sp. BIOMIG1, which is a bacterium present in various env

196 lative abundance of a particular Pseudomonas sp. strain, BIOMIG1.

197 ater lake environments, and that Pseudomonas sp. populations are critical participants.

198 ly well-preserved specimen of Psittacosaurus sp. from the Chinese Jehol biota [16, 17].

199 These studies suggest that Psittacosaurus sp. inhabited a closed habitat such as a forest with a r

200 ms consisting of purely sp (3) bonds, purely sp (3)-bonded tetrahedral amorphous carbon has not yet b

201 ine and amorphous forms consisting of purely sp (3) bonds, purely sp (3)-bonded tetrahedral amorphous

202 whereas the treatment with fungus Pycnoporus sp. and Trametes versicolor increased qm up to 72.5 mg/g

203 rmation in Caenorhabditis elegans, Rhabditis sp. SB347 (recently named Auanema rhodensis) and related

204 dase from the Alphaproteobacterium Rhizobium sp. NT-26 using a combination of X-ray absorption spectr

205 fungal genera were Aspergillus sp., Rhizopus sp., Penicillium sp. and Sarocladium sp., occurring at 3

206 miltonella defensa, Regiella + Rickettsiella sp., Regiella + Spiroplasma sp.) and strains (Hamiltonel

207 CFU/mL and 11.7 x 10(3)CFU/mL for Salmonella sp., respectively.

208 of detecting E. coli O157:H7 and Salmonella sp. in complex hamburger and cucumber samples with extra

209 ltaneous detection of E. coli and Salmonella sp. in hamburger sample using a multichannel SPR biosens

210 The fish used was sardine (Sardinella sp.) where the production of eight biogenic amines was m

211 hizopus sp., Penicillium sp. and Sarocladium sp., occurring at 37, 18, 13 and 12% respectively.

212 experiments were conducted with Scenedesmus sp. and Chlorella sp. in the presence and absence of car

213 The bivalved euarthropod Clypecaris serrata sp. nov., recovered from the Cambrian (Stage 3) Hongjing

214 teria, such as the enterobacterium, Serratia sp. ATCC 39006 (S39006).

215 from Fe-reducibility assays using Shewanella sp., however was undetectable by chemical extractions, M

216 l exudate (IRI-160AA) produced by Shewanella sp. IRI-160 that is effective against dinoflagellates, w

217 Of the 1,982 Escherichia coli and Shigella sp. isolates analyzed in this study, 1,957 (98.4%) had c

218 ding a homolog binned within the 'Smithella' sp. SDB genome scaffold, were detected via RT-PCR, imply

219 ncludes known virulence factors (mntE, speB, spd, nga [spn], prtS [SpyCEP], and sse) and cell surface

220 tion of Mbn from Methylosinus (Ms.) species (sp.) LW4.

221 Sphingobium sp. SYK-6 is a soil bacterium boasting a well-studied li

222 Strain SYK-6 of the bacterium Sphingobium sp. catabolizes lignin-derived biphenyl via a meta-cleav

223 s been reported in the bacterium Sphingobium sp. SYK-6.

224 ependent phosphotriesterase from Sphingobium sp. strain TCM1 that is capable of hydrolyzing organopho

225 in lignin has been identified in Sphingobium sp. SYK-6 bacteria.

226 A net loss of Sphingobium sp. BiD32 was observed in the reactors, supporting the o

227 st reactor was bioaugmented with Sphingobium sp. BiD32, a documented BPA-degrading culture.

228 Immobilized biohybrid of Sphingomonas sp.-(f)Si NP was characterized using SEM.

229 Biohybrid of Sphingomonas sp.-(f)Si NP was immobilized on the wells of microplate

230 The previously developed Sphingomonas sp. based optical microplate biosensor for methyl parath

231 i NP) were then integrated with Sphingomonas sp. cells.

232 + Rickettsiella sp., Regiella + Spiroplasma sp.) and strains (Hamiltonella) that we studied.

233 ty of liposomal systems containing Spirulina sp. LEB-18 phenolic extract (PE) against Fusarium gramin

234 res, and 16 OTUs, including a Staphylococcus sp. were significantly more abundant in Tumaco.

235 an pathogens Aeromonas sp., Stenotrophomonas sp. and an unculturable bacterium.

236 d from laboratory cultures of a Streptomyces sp. obtained from a tropical marine sediment.

237 d from laboratory cultures of a Streptomyces sp. Svetamycins A-D, F, and G are cyclic depsipeptides,

238 elationship between CLI2509 and Streptomyces sp. SPB78, which was previously implicated in an insect-

239 ruction in the marine bacterium Streptomyces sp. CNB-091, which involves a novel intermolecular trans

240 or herbicidin A biosynthesis in Streptomyces sp. L-9-10 as well as its verification by heterologous e

241 actone azalomycin F in mangrove Streptomyces sp. 211726 has shown that only nineteen extension module

242 characterized as metabolites of Streptomyces sp. AD-23-14 isolated from the Rock Creek underground co

243 actin (3) in a crude extract of Streptomyces sp. AMC 23 in the precursor ion scan mode.

244 nigericin in a crude extract of Streptomyces sp. Eucal-26 by means of precursor ion scan experiments,

245 One bacterial strain (Streptomyces sp. CLI2509) from the bracket fungus Hymenochaete rubigi

246 from the model cyanobacterium Synechococcus sp. PCC 7002 grown under 42 different conditions was ana

247 ogically robust cyanobacterium Synechococcus sp. PCC 7002 to changing environmental variables.

248 ems (Emiliania huxleyi/EhV207, Synechococcus sp. WH8101/Syn1 and Escherichia coli/T7).

249 enables Chl f biosynthesis in Synechococcus sp. PCC 7002.

250 drocarbon-deficient mutants of Synechococcus sp. PCC 7002 and Synechocystis sp. PCC 6803 exhibit sign

251 odel marine picocyanobacterium Synechococcus sp. WH7803 and the Roseobacter strain Ruegeria pomeroyi

252 e lipidome of the model strain Synechococcus sp. WH7803 and its response to temperature variation.

253 vo measurements confirmed that Synechococcus sp. PCC 7002 mutants lacking hydrocarbons exhibit reduce

254 Synechococcus sp. PCC 7002 and Synechocystis sp. PCC 6803 exhibit significant phenotypic differences

255 from Gloeobacter violaceus and Synechocystis sp. PCC6803 obtained by X-ray crystallography showed two

256 residue in the cyanobacterium Synechocystis sp. PCC 6803 (wildtype) with alanine, present in higher

257 eriments on the cyanobacterium Synechocystis sp. PCC 6803 assessed the flexibility of cyanobacterial

258 eered the model cyanobacterium Synechocystis sp. PCC 6803 for sustainable production of a commerciall

259 in of the model cyanobacterium Synechocystis sp. PCC 6803 leads to a unique high-CO2-sensitive phenot

260 The unicellular cyanobacterium Synechocystis sp. PCC 6803 moves with Type IV pili and measures light

261 In the cyanobacterium Synechocystis sp. PCC 6803, the slr1796 gene encodes a single cysteine

262 n for the model cyanobacterium Synechocystis sp. PCC 6803, we performed chromatin immunoprecipitation

263 b28-2, from the cyanobacterium Synechocystis sp. PCC 6803.

264 t of heteromultimeric PntAB in Synechocystis sp. PCC 6803 was inactivated, followed by phenotypic and

265 nobacterial ortholog, cycI, in Synechocystis sp. PCC 6803, but also of ycf54; conversely, coexpressio

266 n Slr1270, a TolC homologue in Synechocystis sp. PCC 6803.

267 ws to the photosynthetic model Synechocystis sp. PCC 6803 and presents a valuable model for studying

268 x in the thylakoid membrane of Synechocystis sp. PCC 6803 (hereafter Synechocystis), the exact roles

269 d the growth and metabolism of Synechocystis sp. PCC 6803 under different nitrogen sources, light int

270 tic electron transfer chain of Synechocystis sp. PCC 6803.

271 cing the native PPTase gene of Synechocystis sp. PCC6803, two selected cyanobacterial PPTases and Sfp

272 photosynthetic model organism Synechocystis sp. PCC 6803 can grow in different trophic modes, depend

273 e DNA templates: Lambda phage, Synechocystis sp. PCC 6803 rbcL gene, and human HFE.

274 cyanobacterium Synechocystis (Synechocystis sp. PCC 6803) has a functional receptor for ethylene, Sy

275 Genome comparison between T. sp. NMC-1 and six relatives showed that functionally unk

276 a much higher proportion (28.12%) of the T. sp. NMC-1 genome.

277 nvestigate the genetic mechanism by which T. sp. NMC-1 adapted to the specific environment.

278 mented plates) were identified as Tannerella sp. HOT-286.

279 im of this study was to cultivate Tannerella sp. HOT-286.

280 One such taxon, Tannerella sp. HOT-286 (phylotype BU063), is the focus of much inte

281 , Phaeodactylum tricornutum, and Tetraselmis sp. were selected based on their varying sensitivities t

282 ased 4-fold in C. closterium and Tetraselmis sp. when exposed to copper, but was unchanged in P. tric

283 erature lagoon and identified as Tetraselmis sp. DS3.

284 er thermautotrophicus (Mth) and Thermococcus sp. 9 degrees N (9 degrees N).

285 was distantly related to Thermodesulfovibrio sp. (87-89% 16S rRNA gene identity, 52-54% average amino

286 OT) 274, Fretibacterium sp. HOT 360, and TM7 sp. HOT 356 phylotypes, as well as higher mean levels of

287 HOT 360, Fretibacterium sp. HOT 362, and TM7 sp. HOT 356 phylotypes, in addition to F. alocis, F. fas

288 subjects presented higher mean levels of TM7 sp. HOT 356 and F. alocis than GChP subjects (P < 0.05).

289 cing both elastic deformations and sp (2) to sp (3) chemical changes.

290 couple under palladium catalysis leading to sp-, sp(2) -, and sp(3) -substituted arrays.

291 fungal isolates, including the Tolypocladium sp. strain that produced pericoxide and pericosine A.

292 cally acclimating cyanobacterium Tolypothrix sp. PCC 7601, which encodes both OCP1 and OCP2 as well a

293 genome sequence of cyanobacteria Trichormus sp. NMC-1 in the QTP and performed whole transcriptome s

294 (OTUs), Leptotrichia wadei and a Veillonella sp., were significantly more abundant in Tuquerres, and

295 ukaryotic more closely related to Vermamoeba sp., were each isolated in one solution.

296 Colpoda sp., Protostelium sp. and Vermamoeba sp. are reported for the first time as contaminating con

297 eralist saprophytic marine bacterium (Vibrio sp. F13 9CS106) on complex resources derived from its na

298 the physiological characteristics of Vibrio sp. B2 and biofilm formation on nanofiltration (NF) memb

299 ific hybrid wine was studied using the Vitis sp. 'Frontenac' and 'Vidal'.

300 The presence of Wolbachia sp. was shown for the first time in the wild-caught sand