ライフサイエンスコーパス: sp.

1 n, we engineered an enhanced Acidaminococcus sp. Cas12a variant (enAsCas12a) that has a substantially

2 re and enrichment cultures of Acidimicrobium sp. strain A6 (A6), an autotroph that oxidizes ammonium

3 by AXDX using 101 contemporary Acinetobacter sp. clinical isolates.

4 ate-3-phosphate synthase, from Agrobacterium sp. strain CP4 (CP4 EPSPS), which confers glyphosate tol

5 tly insects), highly adapted fish (Alcolapia sp.), and birds including flamingos.

6 Strain F2 was identified as Alishewanella sp., named Alishewanella sp. F2.

7 ed as Alishewanella sp., named Alishewanella sp. F2.

8 Pseudoalteromonas atlantica and Alteromonas sp, it remained nearly intact in the Marinobacterium jan

9 ia (Pseudoalteromonas atlantica, Alteromonas sp., Marinobacterium jannaschii, Amphritea japonica) wer

10 eet (Beta vulgaris) and amaranth (Amaranthus sp.) microgreens.

11 ide intertidal benthic foraminifera (Ammonia sp. (T6), Haynesina sp. (S16) and Elphidium sp. (S5)), u

12 , Rhodoccocus jostii RHA1, and Amycolatopsis sp. ATCC 39116.

13 ptide repeat protein - All4981 - in Anabaena sp. PCC 7120 that polymerized into filaments in vitro an

14 inase in the soil bacterium Anaeromyxobacter sp. Fw109-5.

15 fixing bacteria Bradyrhizobium sp. BTAi1 and sp. ORS278, has been achieved in 25 steps in an overall

16 saurid, Dineobellator notohesperus, gen. and sp. nov., consisting of a partial skeleton from the Uppe

17 the aggressively dominant ant (Aphaenogaster sp.) treatment than in the better discoverer ant M. rubr

18 ring and dispersing seeds, but Aphaenogaster sp. was dominantly aggressive over M. rubra.

19 he high-quality seed disperser Aphaenogaster sp. in its invaded range.

20 new species, namely as Micromonospora arida sp. nov. and Micromonospora inaquosa sp. nov., respectiv

21 Half of the corals were fed Artemia sp. brine shrimp in a separate feeding tank to prevent b

22 hipworm Trichuris sp., the roundworm Ascaris sp., the flatworm Dicrocoelium sp. and the fish tapeworm

23 ributed to loss of their milkweed (Asclepias sp.) host-plants after the introduction of herbicide-tol

24 en alkaline protease 1 (Alp1) of Aspergillus sp., because proteases are critical components of many a

25 (n = 4); three patients cultured Aspergillus sp. in BAL fluid.

26 reductase, NfoR, from Staphylococcus aureus sp. LZ-01 was augmented 1.5-fold by Cu(II).

27 sp. isolates were also inhibited by Bacillus sp. strains in TTC presence, to a lesser extent.

28 etail, an aldoxime dehydratase from Bacillus sp. OxB-1 was used as a biocatalyst for a dehydration of

29 rmation of nitrogenous compounds in Bacillus sp. cells as the plausible cause of the inducible antago

30 e-saturation mutagenesis library of Bacillus sp. MN chitosanase consisting of 167 muteins, enzymes th

31 showed expansion of colitogenic Bacteroides sp. in Itch(-/-) mice.

32 Calumma and a new species, Calumma benovskyi sp. nov., is erected for it.

33 ncludes aurochs and bison (Bos sp. and Bison sp.).

34 tion of molecular screening for Blastocystis sp. at our stool bank identified 2 donors with prior neg

35 Potential transmission of Blastocystis sp. to patients was assessed on 16 fecal patient samples

36 Potential transmission of Blastocystis sp. to patients was assessed on 16 fecal patient samples

37 Patients transferred with Blastocystis sp. positive donor feces did not report any significant

38 from patients transferred with Blastocystis sp.-negative donor feces (93%, 76/82).

39 Patients transferred with Blastocystis sp.-positive donor feces did not report any significant

40 clade, which includes aurochs and bison (Bos sp. and Bison sp.).

41 the nitrogen-fixing bacteria Bradyrhizobium sp. BTAi1 and sp. ORS278, has been achieved in 25 steps

42 mical defense of the host, the alga Bryopsis sp., against predation.

43 For CF candidates, any Burkholderia sp. (hazard ratio [HR], 2.8; 95% confidence interval [CI

44 how that reduction of MAs(V) by Burkholderia sp. MR1 produces toxic MAs(III) that inhibits growth of

45 anometallic nucleophiles to form C(sp (3))-C(sp (2)) bonds.

46 -group organometallic nucleophiles to form C(sp (3))-C(sp (2)) bonds.

47 ormation of C(sp(2))-C(sp(2)) and C(sp(3))-C(sp) bonds, was originally achieved for the design of a n

48 closing metathesis, Lindlar reduction, and C(sp)-C(sp(3)) coupling makes this strategy applicable for

49 nin-2 based on ring-closing metathesis and C(sp)-C(sp(3)) Sonogashira coupling with a 36.5% overall y

50 affords the corresponding C(sp)-C(sp) and C(sp)-C(sp2) coupled products RC=C-C=CAr and Ph-C=CAr with

51 o [Cu(II)]-C=CAr affords the corresponding C(sp)-C(sp) and C(sp)-C(sp2) coupled products RC=C-C=CAr a

52 The related C-H bonds here include C(sp)-H, C(sp2)-H, and C(sp3)-H bonds.

53 Radical capture represents the key C(sp)-C(sp3) bond-forming step in the copper-catalyzed C-H

54 R' (R' = (hetero)aryl, silyl) that provide C(sp)-C(sp3) coupled products R-C=CR via radical relay wit

55 II)]-C=CAr affords the corresponding C(sp)-C(sp) and C(sp)-C(sp2) coupled products RC=C-C=CAr and Ph-

56 of both inter- and intra-molecular direct C((sp)(2))-H arylations of unactivated arenes in a single r

57 es both inter- and intra-molecular direct C((sp)(2))-H arylations of unactivated arenes in the presen

58 pulation of C. medius that we refer to as C. sp. cf. medius.

59 -caught individuals representing species: C. sp. cf. medius, C. major, C. crossleyi, and C. sibreei.

60 ., K. marcocurinii sp. nov., K. carlosrochai sp. nov. and K. ulfjondeliusi sp. nov.

61 active antitumor constituent of Chaetomorpha sp.; other anticancer compounds identified were Oximes a

62 hemical constituents in Seaweed Chaetomorpha sp. extracts has received attention for their role in th

63 A few bacteria including Chelativorans sp. BNC1 can degrade EDTA with a monooxygenase to ethyle

64 he small intestinal pGP3-deficient Chlamydia sp. failed to reach the large intestine, explaining the

65 ng the lack of live pGP3-deficient Chlamydia sp. in rectal swabs following an oral inoculation.

66 ne, suggesting that pGP3-deficient Chlamydia sp. might be able to activate an intestinal resistance f

67 on, suggesting that pGP3-deficient Chlamydia sp. might be prevented from spreading from the small int

68 he gastric barrier, pGP3-deficient Chlamydia sp. still failed to reach the large intestine, although

69 ssues revealed that pGP3-deficient Chlamydia sp. survived significantly better than plasmid-free Chla

70 Interestingly, pGP3-deficient Chlamydia sp. was able to colonize the colon following an intracol

71 ificantly better than plasmid-free Chlamydia sp. in small intestinal tissues.

72 similarly inoculated plasmid-free Chlamydia sp. was able to do so.

73 ouse small intestine, plasmid-free Chlamydia sp. was no longer able to spread to the large intestine,

74 ss, orally inoculated plasmid-free Chlamydia sp. was still able to colonize the gut.

75 Surprisingly, orally inoculated Chlamydia sp. deficient in only plasmid-encoded pGP3 was no longer

76 testinal resistance for regulating Chlamydia sp. spreading.

77 The unicellular green alga Chlamydomonas sp. ICE-L thrives in polar sea ice, where it tolerates e

78 The Antarctic green alga Chlamydomonas sp. UWO 241 (UWO 241) is adapted to permanent low temper

79 ng of thylakoid membranes from Chlamydomonas sp. UWO241 exhibited a distinct low temperature-dependen

80 Chlorella sp. + PSO coatings retarded ripening, maintained firmnes

81 ity of copper to the tropical alga Chlorella sp. was compared.

82 using edible coatings composed of Chlorella sp. and pomegranate seed oil (PSO) during cold storage.

83 of triclosan to green microalga Chlorococcum sp. under multiple interactions among multiple environme

84 biodinium tridacnidorum (A3) and Cladocopium sp. (C).

85 Cladosporium sp., Pseudogymnoascus roseus, Leotiomycetes sp. 2, Penic

86 Enterobacter sp. A11 and Comamonas sp. A23 were isolated and identified.

87 ocument the cultivation of squash (Cucurbita sp.) at about 10,250 calibrated years before present (ca

88 egulated in the response to both Curvibacter sp., the main bacterial colonizer of Hydra, and low temp

89 Here, we report a denitrifying Denitratisoma sp. strain DHT3 capable of catabolizing estrogens or and

90 haera spp., Sneathia spp., BVAB-2, Dialister sp. type 2.

91 Diaphorobacter sp. strain JS3050 utilizes 3,4-DCNB as a sole source of

92 dworm Ascaris sp., the flatworm Dicrocoelium sp. and the fish tapeworm Diphyllobothrium sp.

93 s awaiting trophic transmission (Diplostomum sp. and Diphyllobothrium spp.) and negatively associated

94 bfossil plants and beaver collagen (Dipoides sp.) from the Early Pliocene, High Arctic Beaver Pond fo

95 re Island), in order to reconstruct Dipoides sp. diet.

96 patens (Plantae), the brown alga Ectocarpus sp. (Chromista), and the ascomycetes Neurospora crassa a

97 Yaukthwa elongatula sp. nov., a peculiar species, conchologically resembling

98 sp. (T6), Haynesina sp. (S16) and Elphidium sp. (S5)), using a metabarcoding approach targeting the

99 8) is described here as Blastomyces emzantsi sp. nov.

100 We found that the presence of Entamoeba sp., a commensal gut protozoan, followed by stool consis

101 Enterobacter sp. A11 and Comamonas sp. A23 were isolated and identifi

102 In an infection with an Enterobacter sp. isolate producing Klebsiella pneumoniae Carbapenemas

103 urrence of an infection with an Enterobacter sp. isolate producing KPC-4 and NDM-1 in the US.

104 ms between Pb(2+) and Cd(2+) in Enterobacter sp. Microbial respiration and production of formic acid

105 tion of formic acid showed that Enterobacter sp. had a higher tolerant concentration of Pb (>1000 mg

106 tion of formic acid showed that Enterobacter sp. had a higher tolerant concentration of Pb (>1000 mg

107 at propionyl-CoA synthase from Erythrobacter sp. NAP1, as well as an acrylyl-CoA reductase from Nitro

108 uangia, the new taxon Daihua sanqiong gen et sp. nov., and Dinomischus venustus, informally referred

109 which we name Yilingia spiciformis (gen. et sp. nov).

110 ich we name Oculudentavis khaungraae gen. et sp. nov.

111 a new taxon, Elektorornis chenguangi gen. et sp. nov.

112 Here, we describe Ikaria wariootia gen. et sp. nov. from the Ediacara Member, South Australia, a sm

113 Cyathinema digermulense gen. et sp. nov. from the Nyborg Formation, Vestertana Group, Di

114 early ornithodiran (Kongonaphon kely gen. et sp. nov.) from the Mid-to-Upper Triassic of Madagascar t

115 w theropod, Yunyangosaurus puanensis gen. et sp. nov., based on a fragmentary specimen recovered from

116 uropodomorph, Irisosaurus yimenensis gen. et sp. nov., from the Early Jurassic Fengjiahe Formation of

117 zed stem bird, Falcatakely forsterae gen. et sp. nov., from the Late Cretaceous epoch of Madagascar t

118 Asteriornis maastrichtensis, gen. et sp. nov., from the Maastrichtian age of Belgium (66.8-66

119 w hadrosaurid, Kamuysaurus japonicus gen. et sp. nov., was discovered from the outer shelf deposits o

120 from Mongolia, Zuunia chimidtsereni gen. et sp. nov., which exhibits key characteristics of submicro

121 neage of insect, Mesophthirus engeli gen et. sp. nov. within Mesophthiridae fam. nov. from the mid-Cr

122 Here we describe Kylinxia zhangi gen. et. sp. nov., a euarthropod from the early Cambrian Chengjia

123 y powdery mildew fungus Blumeria graminis f. sp. hordei (Bgh).

124 barley fungal pathogen Blumeria graminis f. sp. hordei PCS1, which is found in the cytoplasm of cell

125 nce to Ps. japonica and Blumeria graminis f. sp. hordei, indicating a conserved role of the pathway.

126 ens Puccinia hordei and Blumeria graminis f. sp. hordei, which cause leaf rust and powdery mildew, re

127 ungal disease caused by Blumeria graminis f. sp. tritici (Bgt), has a serious impact on wheat product

128 wdery mildew, caused by Blumeria graminis f. sp. tritici (Bgt), is one of the most destructive diseas

129 eat stem rust pathogen, Puccinia graminis f. sp. tritici (Pgt), such as Ug99, are a major threat to g

130 heat stem rust pathogen Puccinia graminis f. sp. tritici (Pgt), suppress RNA silencing in plants and

131 onse against stem rust (Puccinia graminis f. sp. tritici) pathogens.

132 ly, Podospora anserina, Puccinia graminis f. sp. tritici, and Pestalotiopsis sp.

133 gene (FUB) cluster in Fusarium oxysporum f. sp. cubense tropical race 4 (Foc TR4) reduced the FSA pr

134 SNARE protein Vam7p in Fusarium oxysporum f. sp. lycopersici (Fol), a fungal pathogen of tomato.

135 a soilborne pathogen, Fusarium oxysporum f. sp. radicis lycopersici.

136 m rust, caused by Puccinia graminis Pers. f. sp. tritici (Pgt), is a devastating fungal disease threa

137 tors enhance defense against Pneumocystis f. sp. murina, though it is unclear whether antibodies reac

138 mmon wheat and one race of P. striiformis f. sp. hordei in barley.

139 due to infection by Puccinia striiformis f. sp. tritici (Pst), is a devastating disease that causes

140 escribed species (here named Choanoeca flexa sp. nov.) that forms multicellular cup-shaped colonies.

141 icola, Prevotella intermedia, Fretibacterium sp. HOT360 and lower levels of Rothia dentocariosa were

142 cteria (Eubacterium saphenum, Fretibacterium sp. human oral taxon(HOT) 360, TM7 sp. HOT 356, and Roth

143 first time, the filamentous fungus Fusarium sp. was utilized for devising a novel method for pre-con

144 d Anthriscus sylvestris (hap C); one Gallium sp. (Rubiaceae) (hap undetermined); and Chenopodium albu

145 Geobacillus sp. WSUCF1 is a Gram-positive, spore-forming, aerobic an

146 red capabilities of thermophilic Geobacillus sp. strain WSUCF1 to generate electricity directly from

147 Tsetse flies (Glossina sp.) are the vectors of human and animal trypanosomiasis

148 The weakly electric fish, Gymnotus sp., uses its active electric sense during navigation in

149 a anguilla, and the whirligig beetle Gyrinus sp.) had been extirpated.

150 kull and mandible of Clevosaurus hadroprodon sp. nov., a new taxon of sphenodontian lepidosaur from t

151 found a Streptococcus sp. and a Haemophilus sp. were the most relatively abundant pathogens.

152 the chitinolytic haloarchaeon Halomicrobium sp. LC1Hm.

153 h to glucose enabled growth of Halomicrobium sp. LC1Hm in the absence of a chitin.

154 ic foraminifera (Ammonia sp. (T6), Haynesina sp. (S16) and Elphidium sp. (S5)), using a metabarcoding

155 New Zealand native edible mushroom Hericium sp., a high-performance liquid chromatography coupled wi

156 attributed to Paranthropus) and Stw 80 (Homo sp.), show similarities to the species, and we discuss a

157 specimen (StW 311) attributed to either Homo sp. or Paranthropus robustus exhibits a pattern more sim

158 a separate species (Tanystropheus hydroides sp. nov.).

159 a arida sp. nov. and Micromonospora inaquosa sp. nov., respectively.

160 ty, common-ion effect, pK(a), pH(max), and K(sp) values of three model compounds in a fast and low sa

161 gent (ASR) assay adds a second Lactobacillus sp. target, and the recently cleared in vitro diagnostic

162 on-Chagas were negative, and 1/12 Leishmania sp. was positive.

163 Here, we show that 'Lentimonas' sp. CC4, belonging to the Verrucomicrobia, acquired a re

164 sp., Pseudogymnoascus roseus, Leotiomycetes sp. 2, Penicillium sp., Mortierella sp. 1, Mortierella s

165 the thermophilic cyanobacterium Leptolyngbya sp. JSC-1 that is a representative member of a phylogene

166 Several taxa including Sneathia amnii-like sp., Peptoniphilaceae [G-1] bacterium HMT 113, Porphyrom

167 E. coli, S. aureus, Salmonella sp., Listeria sp., yeast and moulds, making it an ideal candidate for

168 Lupine (Lupinus sp.) is a valuable source of plant proteins.

169 tors; the numbers of the leafminer Lyriomyza sp. directly increased with the numbers of spiders.

170 yr BP), manioc (Manihot sp.) at about 10,350 cal.

171 osed: Kryptodasys gen. nov., K. marcocurinii sp. nov., K. carlosrochai sp. nov. and K. ulfjondeliusi

172 o the Antarctic marine bacterium Marinomonas sp. BSw10506 and the sub antarctic Marinomonas polaris.

173 We named this new strain Marinomonas sp. ef1.

174 After the Marinomonas sp. ef1 biomass incubation with 1 mM of AgNO(3) at 22 de

175 australis, Otaria flavescens and Merluccius sp.) significantly increased their trophic levels.

176 ilus., Pantoea agglomerance., Microbacterium sp., and Serratia marcescens), and their nine mixture tr

177 icillium sp., Mortierella sp. 1, Mortierella sp. 2, Pseudogymnoascus appendiculatus and Pseudogymnoas

178 omycetes sp. 2, Penicillium sp., Mortierella sp. 1, Mortierella sp. 2, Pseudogymnoascus appendiculatu

179 A previously undescribed Mycoplasma sp. sequence was found in two guignas and one cat.

180 s in PUFA were obtained with Nannochloropsis sp. (207.9 mg/g of oil) using 0.4% wt of chitosan and 1:

181 irchneriella subcapitata and Nannochloropsis sp. at different biomass/ethanol/chitosan ratios.

182 and in smaller dark granules in Neoditomiya sp, consists of a high molecular weight complex of lucif

183 ed photoautotrophic cyanobacterium Nodularia sp. and potential cold adapted members of the alphaprote

184 f the complex from the cyanobacterium Nostoc sp. revealed the presence of 23 lipid-binding sites per

185 ew order, Ca. Lunaplasma lacustris ord. nov. sp. nov.

186 raders, Sphingomonas sp. and Novosphingobium sp., was detected in the alpha-HCH-treated rhizosphere s

187 Here we report Dactylobiotus ovimutans sp. nov. from King George Island, Antarctica.

188 ids in the plant-associated bacteria Pantoea sp. YR343 results in changes to membrane biophysical pro

189 deletion of carotenoid production in Pantoea sp. YR343 results in altered membrane protein distributi

190 We show that DMFase from Paracoccus sp. strain DMF is a halophilic and thermostable enzyme c

191 wo strains of SAR11, Candidatus Pelagibacter sp. HTCC7211 and Cand.

192 cus roseus, Leotiomycetes sp. 2, Penicillium sp., Mortierella sp. 1, Mortierella sp. 2, Pseudogymnoas

193 high antifungal efficacy against Penicillium sp. and Aspergillus niger but low effective against Rhiz

194 s, Cladosporium, Mortierella and Penicillium sp. were the most dominant ASVs detected in the air in r

195 ic (Colletotrichum tropicale, Pestalotiopsis sp., Colletotrichum theobromicola, or Phytophthora palmi

196 assembled genomes (MAGs) of these Petromonas sp. were obtained and used to determine that these popul

197 ception of that of cormorants (Phalacrocorax sp.).

198 th a different coiling geometry, Planorbella sp., we find similar shell margin organization and growt

199 nd the symptomatic blood stage of Plasmodium sp. infection.

200 hase dimers from the green algae Polytomella sp. and the yeast Yarrowia lipolytica into liposomes and

201 by acanthocephalan parasites Pomphorhynchus sp. from differently contaminated riverine sites.

202 laeojavanicus, Pithecanthropus dubius, Pongo sp.).

203 pin-7-sulfate in a subset of poplar (Populus sp.) and willow (Salix sp.) species revealed a broader d

204 ic behavior, switching between a small-pore (sp) structure and a large-pore (lp) structure.

205 tionally large, hermatypic colony of Porites sp. has been identified and measured at Ta'u, American S

206 The capacities of single-positive (sp) KIR2DL1, KIR2DL2, KIR2DL3, and KIR3DL1 NK cells to p

207 mestizos (Mobiluncus mulieris and Prevotella sp.).

208 ctive Type VI-B Cas13 enzyme from Prevotella sp. P5-125 (dPspCas13b) to m6A demethylase AlkB homolog

209 us, Pseudomonas aureginosa, E. coli, Proteus sp. and streptococcus sp.) at concentrations up to 2.5 m

210 ted from marine sediments (Pseudoalteromonas sp. strain CF6-2) can kill Gram-positive bacteria of div

211 mnoascus appendiculatus and Pseudogymnoascus sp. were the most dominant fungi.

212 l monoculture (Pseudomonas poae, Pseudomonas sp., Bacillus pumilus., Pantoea agglomerance., Microbact

213 ese compounds can be traced to a Pseudomonas sp. strain isolated from the frog's skin.

214 plant growth-promoting effect by Pseudomonas sp. CH267.

215 oss of plant growth promotion by Pseudomonas sp. CH267.

216 Amyloid formed by Pseudomonas sp. protein FapC provides an excellent model to investig

217 thalonil dehalogenase (Chd) from Pseudomonas sp. CTN-3, with 15 of its N-terminal residues truncated

218 respiratory organs of Adelophthalmus pyrrhae sp. nov. from the Carboniferous of Montagne Noire, Franc

219 iescent primary human spinal astrocytes (qHA-sps).

220 VZV-infected qHA-sps, but not mock-infected qHA-sps, contained intracellu

221 -infected qHA-sps, but not mock-infected qHA-sps, contained intracellular amylin, APP, and/or Abeta,

222 torey harvesting in overstorey oaks (Quercus sp.), so-called standards.

223 We demonstrate that R. sp. IRBG74 can be engineered to result in nitrogenase ac

224 zorhizobium caulinodans ORS571 and Rhizobium sp. IRBG74) and the well-characterized plant epiphyte Ps

225 w an extracellular fungal protease (Rhizopus sp.) hydrolyzed iron oxide-associated bovine serum album

226 et of poplar (Populus sp.) and willow (Salix sp.) species revealed a broader distribution within the

227 gens, such as E. coli, S. aureus, Salmonella sp., Listeria sp., yeast and moulds, making it an ideal

228 s Scalindua rubra" and "Candidatus Scalindua sp. SCAELEC01 167" possess different architectures than

229 lutein recovery from microalgae Scenedesmus sp. biomass.

230 Micro-algae, Schizochytrium sp., is rich source of docosahexaenoic acid, DHA (66%-li

231 ffects of dietary algal meal (Schizochytrium sp., AM) and micro-minerals (MM, either organic [OM] or

232 cosahexaenoic acid (DHA)-rich Schizochytrium sp. as substitute for fish oil.

233 s consumed tPOC (dominated by Schoenoplectus sp., or tule) even when phytoplankton were abundant and

234 direct effects through its host plant (Sedum sp.).

235 ficantly reduced with the inclusion of Sedum sp. and in dry-climate scenarios which resulted in a red

236 Serratia sp. ATCC 39006 produces intracellular gas vesicles to en

237 on by a novel Shewanella isolate, Shewanella sp. (NR), in batch incubations.

238 ng a lambda Red Beta homolog from Shewanella sp. W3-18-1.

239 igh abundance of HCH degraders, Sphingomonas sp. and Novosphingobium sp., was detected in the alpha-H

240 f carotenoid extract obtained from Spirulina sp. LEB 18 by nanoprecipitation, using poly (d)(,)(l)(-)

241 ined with biomass of the microalga Spirulina sp. LEB 18.

242 Paraconiothyrium sporulosum and Stagonospora sp., we observed that aerobic Se(IV and VI) bioreduction

243 Escherichia coli and Staphylococcus sp. isolates were also inhibited by Bacillus sp. strains

244 nst R. solanacearum, E. coli, Staphylococcus sp. and B. subtilis, and exhibited activity against path

245 and entomopathogenic nematodes (Steinernema sp., Heterorhabditis).

246 tes, which are produced by Streptacidiphilus sp. P02-A3a, isolated from decaying pinewood.

247 Streptomyces resistomycificus, Streptoccocus sp. GMD2S, Pseudoalteromonas luteoviolacea, and Ktedonob

248 nosa, E. coli, Proteus sp. and streptococcus sp.) at concentrations up to 2.5 mg/ml with inhibition a

249 Rothia mucilaginosa, Streptococcus sp., and Veillonella parvula were selected as important

250 s from 77 patients and found a Streptococcus sp. and a Haemophilus sp. were the most relatively abund

251 Streptomyces sp. Kz-24 (GenBank accession no. KY000533; 1367 bp) show

252 Streptomyces sp. PB-79 (GenBank accession no. KU901725; 1313 bp), Str

253 sion no. KY000536; 1377 bp) and Streptomyces sp. Kz-67 (GenBank accession no. KY000540; 1383 bp) show

254 cession no. KU901725; 1313 bp), Streptomyces sp. Kz-28 (GenBank accession no. KY000534; 1378 bp), Str

255 cession no. KY000534; 1378 bp), Streptomyces sp. Kz-32 (GenBank accession no. KY000536; 1377 bp) and

256 e natural product isolated from Streptomyces sp. RKND-216.

257 II PKS gene cluster (skt) from Streptomyces sp. Tu 6314.

258 n of the cytochrome P450, NzeB (Streptomyces sp. NRRL F-5053), which catalyzes both intermolecular ca

259 Therefore, the genome of Streptomyces sp. RKND-216 was sequenced to identify the levesquamide

260 product of ginseng-rhizospheric Streptomyces sp. WON17.

261 The strain Streptomyces sp. So13.3 showed the greatest antibiotic activity (MIC

262 quence of the oil field isolate Sulfurimonas sp. strain CVO and compared its gene expression during n

263 onfinement of actively growing Synechococcus sp. PCC 7002 cells leads to the physical disassociation

264 The phycobilisomes of Synechococcus sp. RS9916 contain two forms of the protein phycoerythri

265 ress-acclimated monoculture of Synechocystis sp., which rapidly grew and flourished in wastewater, wi

266 Synechocystis sp. PCC 6803 has four FDPs (Flv1-4), which are essential

267 rmosynechococcus elongatus and Synechocystis sp. in their free forms, and in complex with the nicotin

268 luated in Escherichia coli and Synechocystis sp. PCC 6803.

269 hococcus elongatus PCC7942 and Synechocystis sp. PCC6803.

270 tially invasive cyanobacteria (Synechocystis sp. PCC6803).

271 tablished model cyanobacterium Synechocystis sp. PCC 6803 and the more recently described fast-growin

272 achinery of the cyanobacterium Synechocystis sp. PCC 6803 resides in flattened membrane sheets called

273 d growth of the cyanobacterium Synechocystis sp. PCC 6803 using a reproducible cultivation setup.

274 w here that the cyanobacterium Synechocystis sp. PCC6803 accumulates both triacylglycerol and wax est

275 embranes of the cyanobacterium Synechocystis sp. PCC6803 to elucidate the action of Ca(2+) and periph

276 ding the model cyanobacterium, Synechocystis sp. PCC6803), so maintenance of UmuD at low levels must

277 the imSyn617 mapping model for Synechocystis sp. PCC 6803 (Synechocystis 6803) as the starting point

278 F) plays a pleiotropic role in Synechocystis sp. PCC 6803 physiology, with a major impact on growth a

279 Asp (DEAD)-box RNA helicase in Synechocystis sp. PCC 6803, crhR (slr0083), increases 15-fold.

280 In Synechocystis sp. PCC 6803, the global nitrogen regulator NtcA activat

281 dentifying ~67% of proteins in Synechocystis sp. PCC 6803, ~1000 more than previous studies.

282 erminus of the UmuD protein in Synechocystis sp. PCC6803, which is distinct from the degron required

283 acteria, since many, including Synechocystis sp. PCC 6803, conduct photosynthesis and respiration in

284 CycleSyn, a periodic model of Synechocystis sp. PCC 6803 metabolism that spans a 12-hr light/12-hr d

285 ted the undulation dynamics of Synechocystis sp. PCC 6803 thylakoids under normal photosynthetic cond

286 Therefore, this strain of Synechocystis sp. shows great promise for use in phycoremediation, wit

287 a wiggsiae, Treponema sp. HOT268, Tannerella sp. HOT286, Veillonella gp.1 compared with the CCC-haplo

288 d changed over the last 50 years for Taonius sp. B (Voss), Gonatus antarcticus, Galiteuthis glacialis

289 od but, of the five species, only in Taonius sp. B (Voss) did these indices correlate with, delta(13)

290 gate histidine residue (H931 in Thermococcus sp. 9 degrees N PolD) in the PolD s-motif both prevents

291 bacterium sp. human oral taxon(HOT) 360, TM7 sp. HOT 356, and Rothia dentocariosa), and cultivable ba

292 by S. mutans, Scardovia wiggsiae, Treponema sp. HOT268, Tannerella sp. HOT286, Veillonella gp.1 comp

293 f the rickettsial endosymbiont of Trichoplax sp. H2 (strain "Panama").

294 lyses, to show that the placozoan Trichoplax sp. H2 lives in symbiosis with two intracellular bacteri

295 r humans and animals: the whipworm Trichuris sp., the roundworm Ascaris sp., the flatworm Dicrocoeliu

296 . carlosrochai sp. nov. and K. ulfjondeliusi sp. nov.

297 to osmotic shock extracts and complete Ulva sp. proteome, extracted with the thermochemical method.

298 ology model of Wsp.Man26A from Westerdykella sp. and the sequences of nine other fungal GH26 endomann

299 ding formate dehydrogenase from Xanthobacter sp. 91 (XaFDH), into a metabolic pathway expressed in Es

300 By coupling Xenia sp. regeneration and single-cell RNA sequencing, we obse