ライフサイエンスコーパス: symbiotic

1 ylus keniensis) and invertebrate (a guild of symbiotic Acacia ants) animal species in a semi-arid Ken

2 mbiotic larval stage (32-49% higher) and the symbiotic adult life stage (51% higher).

3 Analyzing genetic diversity of symbiotic algae across >5,000 km of the PAG, the Gulf of

4 coral animal in concert with its unicellular symbiotic algae and a wide diversity of closely associat

5 phs, such as plants and mycorrhizal fungi or symbiotic algae and corals, underpin the functioning of

6 zed the contribution of both animal host and symbiotic algae to thermal tolerance in corals that have

7 enetic divergence in both the coral host and symbiotic algae.

8 tion are potential negative ramifications of symbiotic alliances.

9 AraC-like transcription factor CuxR in plant symbiotic alpha-proteobacteria.

10 critical roles in the nitrogen cycle through symbiotic and asymbiotic biological fixation of nitrogen

11 of Bradyrhizobium have been shown to be non-symbiotic and do not possess the ability to form nodules

12 s a versatile fungus with saprophytic, plant symbiotic and insect pathogenic lifestyle options.

13 t of an operational SOS response in presumed symbiotic and parasitic bacteria hints at an intermediat

14 small molecule signals is important for both symbiotic and pathogenic relationships, but is often poo

15 how human neutrophils interact with both the symbiotic and the dysbiotic oral community; an understan

16 ydrogen metabolism, probably associated with symbiotic and/or fermentation-based lifestyles.

17 ccurate differentiation between the healthy (symbiotic) and unhealthy (dysbiotic) microbial state has

18 role of this Amadori compound in pathogenic, symbiotic, and opportunistic bacteria.

19 these different-yet highly complementary and symbiotic-approaches with the view that increased synerg

20 Here we modelled the global diversity of symbiotic arbuscular mycorrhizal (AM) fungi using curren

21 cement can happen even in the most intricate symbiotic arrangements and that preexisting horizontally

22 A complex symbiotic association between legumes and nitrogen-fixin

23 Especially, the symbiotic association between legumes and Rhizobium bact

24 proaches will improve understanding of these symbiotic associations and, in the long term, their usef

25 uscular mycorrhizas (AM) are the most common symbiotic associations between a plant's root compartmen

26 Symbiotic associations in the rhizosphere between plants

27 ty makes this kinase a putative regulator of symbiotic associations involving nutrient acquisition.

28 a presents a particularly large diversity of symbiotic associations that has frequently undergone shi

29 mponent that aid in plant defense and enable symbiotic associations with rhizobia.

30 ction as effector proteins that may regulate symbiotic associations.

31 oblem because of their inherent capacity for symbiotic atmospheric nitrogen fixation, which provides

32 Symbiotic bacteria and mucosal immunoglobulins have co-e

33 reased cellulose degrading activity and that symbiotic bacteria are a rich biochemical and enzymatic

34 Symbiotic bacteria assist in maintaining homeostasis of

35 Symbiotic bacteria decreased plant defenses in all Solan

36 teraction between the host immune system and symbiotic bacteria determines their cooperative rather t

37 Although engineered symbiotic bacteria have been shown to render mosquitoes

38 icrobial gut symbionts and demonstrates that symbiotic bacteria in the gut lumen appear to function a

39 which may contribute to the biogeography of symbiotic bacteria in the gut.

40 ir free-living relatives, mutualistic insect symbiotic bacteria inhabit a static environment where th

41 Our relationship with these symbiotic bacteria is especially important during the ea

42 were more abundant in predatory mites, while symbiotic bacteria prevailed in prey mites.

43 Symbiotic bacteria products are known to modulate differ

44 In addition to metabolic benefits, symbiotic bacteria provide the host with several functio

45 ny insect species harbor obligate, heritable symbiotic bacteria that provision essential nutrients an

46 inate from the microbiome, the consortium of symbiotic bacteria that reside within all animals.

47 Thus, the presence of symbiotic bacteria that suppress plant defenses might he

48 The ability of symbiotic bacteria to inhibit pathogen colonization is m

49 Recognition of symbiotic bacteria via the nucleotide-binding oligomeriz

50 l have orthologs in other phytopathogenic or symbiotic bacteria, and are involved in the modulation a

51 yotes commonly host communities of heritable symbiotic bacteria, many of which are not essential for

52 Most animals host communities of symbiotic bacteria.

53 late the growth of trout total skin and gill symbiotic bacteria.

54 hosts of CPB by chemical elicitors and their symbiotic bacteria.

55 es which inject and feed on entomopathogenic symbiotic bacteria.

56 arbours complex communities of commensal and symbiotic bacterial microorganisms.

57 Bacteroides thetaiotaomicron is a human gut symbiotic bacterium that utilizes a myriad of host dieta

58 We show that a single sponge symbiotic bacterium, Entotheonella sp., constitutes the

59 ermeable channel is known to be required for symbiotic Ca(2+) oscillations, but the calcium channels

60 bia are released from infection threads into symbiotic cells of nodules.

61 onal reprogramming in the differentiation of symbiotic cells.

62 To facilitate the molecular analysis of the symbiotic characteristics of such legumes, we took an in

63 system to control bioluminescence and other symbiotic colonization factors.

64 bacteria undergo during the early stages of symbiotic colonization.

65 The gut harbors many symbiotic, commensal, and pathogenic microbes that break

66 zobial strain, suggesting its involvement in symbiotic communication.

67 animals studied to date are associated with symbiotic communities of microorganisms.

68 the result of a shift of the oral bacterial symbiotic community to a dysbiotic more complex communit

69 The core symbiotic community was composed of Alphaproteobacteria

70 ll focus on determining the function of this symbiotic community, and how it may change during ANG de

71 thetic efficiency was consistently lower for symbiotic compared to autonomous algae, suggesting nutri

72 Individual genomes in these symbiotic complexes differ dramatically in relative abun

73 blished databases of adult and larvae of the symbiotic coral Acropora millepora, revealing both share

74 rs of the Cryptochiridae are small, fragile, symbiotic crabs that live in domiciles in modern corals.

75 to all previously known Cycloclasticus, the symbiotic Cycloclasticus appears to lack the genes neede

76 h similarities between the genes used by the symbiotic Cycloclasticus to degrade short-chain alkanes

77 h chronic skin GVHD and confirm parallel but symbiotic developmental pathways of Th22 and Th17 differ

78 ain promotes colonization of the host by the symbiotic dinoflagellate Symbiodinium minutum.

79 The coral holobiont includes the host, symbiotic dinoflagellates (Symbiodinium spp.), and a div

80 Symbioses between cnidarians and symbiotic dinoflagellates (Symbiodinium) are ecologicall

81 ntially expressed genes (DEGs) for endophyte-symbiotic (E+) vs endophyte-free (E-) clones in leaf bla

82 umen appear to function as partners both for symbiotic EAA supplementation and for digestion of insol

83 gut symbionts also function as partners for symbiotic EAA supplementation is important because the q

84 reduced by competition for nitrogen between symbiotic ectomycorrhizal fungi that associate with plan

85 Stress in the symbiotic environment may arise from three sources: host

86 mphasizes the role of stress as a cue in the symbiotic environment of plants and animals.

87 This review examines the symbiotic, evolutionary, proteomic and genetic basis for

88 With the objective of identifying Frankia symbiotic factors we present a novel approach based on b

89 gatekeeper mutants failed to restore proper symbiotic features in a symrk null mutant where rhizobia

90 conserved throughout evolution(5) and their symbiotic functions preserved, at least between monocot

91 S production in bryophytes could result from symbiotic fungal and bacterial partners that could also

92 lase DWARF14-LIKE (D14L) are involved in pre-symbiotic fungal perception.

93 species, yet interactions between plants and symbiotic fungi (mutualists and potential pathogens) aff

94 Applying the species pool concept to symbiotic fungi facilitated a better understanding of ho

95 1 is required to initiate Ca(2+) spiking and symbiotic gene expression in Medicago truncatula roots i

96 t spread by horizontal transfer of a few key symbiotic genes, converting soil bacteria into legume sy

97 Here we show that the symbiotic genomic idiosyncrasies of ectomycorrhizal basi

98 We report that selective gut symbiotic gram-negative bacteria were able to disseminat

99 We previously showed that symbiotic gut bacteria from CPB larvae suppressed jasmon

100 Symbiotic gut microbiota is essential for human health,

101 The symbiotic gut microbiota play pivotal roles in host phys

102 y plants (UHb) overexpressing the barley non-symbiotic hemoglobin gene HvHb1 that oxidizes NO to NO3(

103 showed that T6SS loci are also widespread in symbiotic human gut bacteria of the order Bacteroidales,

104 identify plant genes required for successful symbiotic infection, we screened an ethyl methanesulfona

105 The symbiotic interaction between legume plants and rhizobia

106 The symbiotic interaction between legumes and nitrogen-fixin

107 is still a poorly characterized step of the symbiotic interaction, as only a few of the genes induce

108 n also is accumulated during early phases of symbiotic interaction, but the pathways involved have no

109 Other 45 were upregulated throughout the symbiotic interaction, from rhizosphere colonization to

110 to both NF and CK signals critical for this symbiotic interaction.

111 olus vulgaris)-Rhizobium tropici (Rhizobium) symbiotic interaction.

112 hich play a key role in the rhizobium-legume symbiotic interaction.

113 nd drought tolerance; and (3) CO2 effects on symbiotic interactions and eco-evolutionary feedbacks.

114 a widely spread perennial herb used to study symbiotic interactions and physiological mechanisms unde

115 lant hormones regulating shoot branching and symbiotic interactions with arbuscular mycorrhizal fungi

116 ous stages of macronutrient deficiencies and symbiotic interactions with rhizobia and mycorrhiza were

117 Legumes develop symbiotic interactions with rhizobial bacteria to form n

118 In legume plants, low-nitrogen soils promote symbiotic interactions with rhizobial bacteria, leading

119 g of tissues as well as for host-parasite or symbiotic interactions.

120 ism and cellular physiology, morphology, and symbiotic interactions.

121 tent with a role in fungal morphogenesis and symbiotic interface differentiation, CAZymes over-expres

122 t is essential for the formation of a stable symbiotic interface in both AM and rhizobium symbiosis.

123 Our results show that vesicle traffic to the symbiotic interface is specialized and required for its

124 s a mutual symbiosis that involves a complex symbiotic interface over which nutrients are exchanged b

125 ovides a model for nutrient exchanges at the symbiotic interface, which may guide future experiments.

126 the intracellular fungus from the apoplatic symbiotic interface.

127 We envisage that the "symbiotic layout" of VisANT can be employed as a general

128 ck of nucleotide biosynthesis capacity and a symbiotic lifestyle.

129 of T. gelatinosa, and perhaps related to its symbiotic lifestyle.

130 also established many novelties due to their symbiotic lifestyle.

131 gration with a bacterial biofilm to obtain a symbiotic-like hybrid - the fabric provides structural f

132 NF induction of the EARLY NODULIN11 (ENOD11) symbiotic marker, while a CK-degrading enzyme (CYTOKININ

133 Symbiotic microbes impact the severity of a variety of d

134 in host defense, but less is known about how symbiotic microbes mediate pathogen-induced damage to ho

135 There is growing evidence that symbiotic microbes play key roles in host defense, but l

136 exchange, as cues for cellular responses in symbiotic microbes.

137 nodules, specialized plant organs containing symbiotic microbes.

138 system to accommodate invasive structures of symbiotic microbes.

139 Symbiotic microbial communities are critical to the func

140 dy describes a mechanism by which the insect symbiotic microbiome offsets gut immunity to achieve hom

141 ic metals, sponges lack organs but harbour a symbiotic microbiome performing various functions.

142 ect of pathogenic bacteria on a host and its symbiotic microbiota is vital and widespread in the biot

143 Consequently, reconstitution of symbiotic microbiota or IL-1alpha ablation markedly amel

144 alterations caused by pathogenic bacteria on symbiotic microbiota using C. elegans as the model speci

145 The trillion symbiotic microorganisms inhabiting the mammalian gastro

146 m pathogens is crucial for plants that allow symbiotic microorganisms to infect and colonize their in

147 These data support a symbiotic model of collective invasion where phenotypica

148 Comparative analyses of wild-type (WT) and symbiotic mutants in Nod factor receptor5 (nfr5), Nodule

149 nt growth phenotypes seen between WT and the symbiotic mutants in nonsupplemented soil were retained

150 t the root-associated community shift in the symbiotic mutants is a direct consequence of the disable

151 dance can help improve the representation of symbiotic N fixation in Earth System Models.

152 mechanisms and optimize N uptake as well as symbiotic N fixation in roots.

153 lant interactions with mycorrhizal fungi and symbiotic N-fixing microbes.

154 ist on low-input agriculture, enabled by the symbiotic N2 -fixation these legumes perform in associat

155 Symbiotic N2 fixation (SNF) brings nitrogen into ecosyst

156 creasing drought frequency, which may affect symbiotic N2 fixation (SNF), a process that facilitates

157 Non-symbiotic N2 fixation appears to be the major source of

158 approach to estimate the contribution of non-symbiotic N2 fixation is robust because it focuses on gl

159 mber of transgenic nodules was increased and symbiotic N2 fixation per nodule was elevated, indicatin

160 ism and partitioning processes in support of symbiotic N2 fixation.

161 genus of Actinobacteria abundant in soil and symbiotic niches, the ability to rapidly degrade cellulo

162 Trees capable of symbiotic nitrogen (N) fixation ('N fixers') are abundan

163 Symbiotic nitrogen (N)-fixing trees can drive N and carb

164 The rarity of symbiotic nitrogen (N)-fixing trees in temperate and bor

165 Iron is critical for symbiotic nitrogen fixation (SNF) as a key component of

166 Symbiotic nitrogen fixation (SNF) occurs in specialized

167 hotosynthesis, induction of root nodules and symbiotic nitrogen fixation and denitrification.

168 f nodule cells and a substantial decrease in symbiotic nitrogen fixation and plant growth.

169 exploring the miR172-mediated improvement of symbiotic nitrogen fixation in common bean, the most imp

170 Iron (Fe) is an essential micronutrient for symbiotic nitrogen fixation in legume nodules, where it

171 nt species with the conspicuous capacity for symbiotic nitrogen fixation in root nodules, specialized

172 has roles within the community not including symbiotic nitrogen fixation.

173 an indirect effect resulting from abolished symbiotic nitrogen fixation.

174 cap and signal motile rhizobia required for symbiotic nitrogen fixation.

175 um cofactor of nitrogenase, is essential for symbiotic nitrogen fixation.

176 Establishment of symbiotic nitrogen-fixation in legumes is regulated by t

177 a test case, we applied this algorithm to a symbiotic nitrogen-fixing bacterium, Sinorhizobium melil

178 Symbiotic nitrogen-fixing trees are thought to provide m

179 The formation of symbiotic nodule cells in Medicago truncatula is driven

180 Cytokinins are required for symbiotic nodule development in legumes, and cytokinin s

181 for receptor-mediated cytokinin signaling in symbiotic nodule organogenesis.

182 hylation was found in only a small subset of symbiotic nodule-specific genes, including more than hal

183 f soil and in the iron-rich environment of a symbiotic nodule.

184 Initiation of symbiotic nodules in legumes requires cytokinin signalin

185 s of postembryonic organs, lateral roots and symbiotic nodules.

186 cibacteria have small genomes and a presumed symbiotic or parasitic lifestyle, but the difficulty in

187 trition to relationships that are commensal, symbiotic, or parasitic.

188 Antioxidant activity of symbiotic organisms known as lichens is an intriguing fi

189 Food webs are replete with similar symbiotic organisms, and we suspect the predator catalys

190 when using metagenomic DNA from inseparable symbiotic organisms, RADseq loci may belong to any numbe

191 d pectinase expression to be enriched in the symbiotic organs, consistent with enzymatic buildup in t

192 the first evidence (to our knowledge) on the symbiotic origins of eukaryotic cells based on the "thir

193 Although over 95% of the symbiotic pairs are economically harmless, there are als

194 study elucidates the evolutionary history of symbiotic palaemonids based on a phylogenetic analysis o

195 signal molecules is a key step to select the symbiotic partner.

196 xpression in the presence and absence of the symbiotic partner.

197 to the striking difference in the choice of symbiotic partners by Mexican and Brazilian Mimosa speci

198 meliloti symbiosis, incompatibility between symbiotic partners frequently occurs, leading to the for

199 They are also critical symbiotic partners in the health of their hosts.

200 and can be used to reinforce the behavior of symbiotic partners that can learn and remember them effe

201 seas is complicated by interactions between symbiotic partners that define stress responses and the

202 lutionary rates in both, rather than single, symbiotic partners.

203 sal mechanisms that drive the recruitment of symbiotic partners.

204 ing interdependencies within this uncultured symbiotic partnership are poorly understood.

205 investigate the role of diverse and mutable symbiotic partnerships in increasing corals' ability to

206 the origins and evolutionary trajectories of symbiotic partnerships remains a major challenge.

207 Organisms across the tree of life form symbiotic partnerships with microbes for metabolism, pro

208 t also impede the establishment of essential symbiotic partnerships.

209 and how its biosynthesis is regulated by the symbiotic pathway.

210 ymbiosis, we tested for correlations between symbiotic persistence and legume distribution, climate,

211 nction to include the negative regulation of symbiotic persistence in host-strain interactions.

212 annual temperatures are associated with high symbiotic persistence in legumes.

213 reads are normal, whereas rhizobia and their symbiotic plant cells become necrotic immediately after

214 s in the formation of root nodules, in which symbiotic plant cells host and harbor thousands of nitro

215 its within the microbial community, a common symbiotic plasmid allows all Rhizobium species to engage

216 However, the symbiotic plasmids are extremely similar, with high rate

217 diated by cell-associated matrices including symbiotic polysaccharide (Syp) and cellulose.

218 econd clade, the species use a Nod-dependent symbiotic process and some of them display a profuse ste

219 dynamics of fixers and non-fixers along the symbiotic process in the Cupriavidus taiwanensis-Mimosa

220 rized by the use of a unique Nod-independent symbiotic process.

221 nts of the Nod-dependent and Nod-independent symbiotic processes, and for comparative analysis of ste

222 tructures and were produced by two different symbiotic Pseudonocardia spp. from ants in the genus Apt

223 lated by DOES NOT MAKE INFECTIONS 2, the key symbiotic receptor kinase of the common symbiosis signal

224 racts with and is phosphorylated by the LYK3 symbiotic receptor kinase, negatively regulates rhizobia

225 eraction with and phosphorylation by two key symbiotic receptor kinases, and downstream signaling via

226 The symbiotic receptor-like kinases nodulation receptor-like

227 ting proteins have been identified for these symbiotic receptor-like kinases, very little is known ab

228 ntial phosphorylation targets for both these symbiotic receptor-like kinases.

229 to map the phosphorylation site(s) of plant symbiotic receptor-like kinases.

230 In order to better understand the symbiotic relationship and cellular cross-talk between H

231 lement each other to cooperatively shape the symbiotic relationship between commensal bacteria and ma

232 les and SWRs and provide novel evidence of a symbiotic relationship between non-REM and REM stages of

233 To maintain a symbiotic relationship between the host and its resident

234 my scientific career entailed dissecting the symbiotic relationship between two membrane transporters

235 al microbiome and immune system are in close symbiotic relationship in health.

236 e mechanisms for planted soybean that have a symbiotic relationship with bacteroids in their root nod

237 ccess atmospheric di-nitrogen (N2) through a symbiotic relationship with rhizobia that reside within

238 It shares a symbiotic relationship with the bacterium Xenorhabdus ne

239 lved multiple means by which to maintain its symbiotic relationship with the microbiota.

240 ingly, CLK1 overcomes this dilemma through a symbiotic relationship with the serine-arginine protein

241 organisms have co-evolved with the host in a symbiotic relationship.

242 Here I discuss examples of these addictive symbiotic relationships and how they are a likely outcom

243 is reveals numerous instances in which these symbiotic relationships are established by alternative,

244 Symbiotic relationships can shape the evolution of the p

245 Symbiotic relationships encompass different lifestyles,

246 Symbiotic relationships promote biological diversificati

247 genome-scale data from organisms involved in symbiotic relationships remains challenging.

248 Several clades of angiosperms have developed symbiotic relationships with actinorhizal bacteria that

249 diverse group of plants that forms elaborate symbiotic relationships with mycorrhizal fungi, and incl

250 legume to study the establishment of binary symbiotic relationships with nitrogen-fixing rhizobia th

251 Given that nearly all tree species form symbiotic relationships with one of two types of mycorrh

252 Moreover, soybean can form symbiotic relationships with Rhizobium bacteria to fix a

253 Fungus-growing ants engage in complex symbiotic relationships with their fungal crop, speciali

254 ep environments, suggests a broader range of symbiotic relationships within AOM consortia than previo

255 But while promoting such symbiotic relationships, plants must restrict the format

256 clade of legumes, indicating a host-specific symbiotic requirement for Mn(2+) transport.

257 These two pre-infection symbiotic responses have been used in combination to sho

258 unable to nodulate, but still exhibit early symbiotic responses including rhizobial infection.

259 roduce, followed by the activation of either symbiotic responses that promote microbial colonization

260 support that MtCEP1 modulates EIN2-dependent symbiotic responses.

261 r nuclear Ca(2+) oscillations and subsequent symbiotic responses.

262 Symbiotic rhizobia in legumes account for a large portio

263 In this context the symbiotic roles of iron trichloride and oxygen in the gu

264 demonstrate uncoupling of symbiosis and the symbiotic root developmental signalling during pre-symbi

265 carboxymethylcellulase, and Cel5A), from the symbiotic rumen Bacteroidetes Prevotella bryantii B14.

266 f the poplar rhizosphere showed evidence for symbiotic sharing of nutrients between the plant and the

267 o our knowledge, a novel common component of symbiotic signaling integrating signal perception throug

268 ependent increase in nodulation requires the symbiotic signaling pathway and ETHYLENE INSENSITIVE2 (E

269 + genotypes included orthologs to some known symbiotic signaling pathway genes, such as NFR5, NSP2, N

270 Different deficiencies at upstream of symbiotic signaling pathway were revealed in the two nod

271 In conclusion, the biologically active symbiotic signals secreted by Frankia appear to be chemi

272 promote ENOD11 expression in the absence of symbiotic signals.

273 nts, and the mechanism of iron uptake within symbiotic soybean root nodules is unknown.

274 Symbiotic species are no longer able to degrade plant ce

275 ance hole size barely changes in specialized symbiotic species, but evolves rapidly once symbiosis wi

276 mostly free-living shrimp, albeit with a few symbiotic species.

277 t that NCR peptides are host determinants of symbiotic specificity in M. truncatula and possibly in c

278 800, that has evolved the ability to control symbiotic specificity.

279 nscription factors may have implications for symbiotic stability, endophyte distribution in the plant

280 ion pattern intermediate between the typical symbiotic state and the aposymbiotic state.

281 sses apparently only occur from a generalist symbiotic state.

282 e regulatory protein NF-kappaB and cnidarian symbiotic status.

283 rge and primarily parasitic communities, and symbiotic sternorrhynchans as examples of generally smal

284 at host-associated niches have selected some symbiotic Streptomyces for increased cellulose degrading

285 basidiomycete Hebeloma cylindrosporum before symbiotic structure differentiation with Pinus pinaster.

286 udy provides the first evidence of extensive symbiotic supplementation of EAA by microbial gut symbio

287 Specifically, we have limited insights into symbiotic syntroph and methanogen ('syntrophy') acid deg

288 norhizobium meliloti and Medicago truncatula symbiotic system, we previously described several natura

289 ively may contribute to the stability of the symbiotic system.

290 ta and shearinines in the fungus-growing ant symbiotic system.

291 Both symbiotic systems are lineage specific and differ in the

292 genes in symbiotic systems, 136 fungi-fungi symbiotic systems were built up by co-culturing seventee

293 nvestigate the expression of silent genes in symbiotic systems, 136 fungi-fungi symbiotic systems wer

294 expect it to be applicable to other similar symbiotic systems, especially other nodule-forming legum

295 olecules, which can be transposable to other symbiotic systems.

296 s that have shaped evolution of this complex symbiotic trait.

297 mploys the promoter of RAM1 as integrator of symbiotic (transmitted via CCaMK and CYCLOPS) and hormon

298 For example, Late Triassic corals have symbiotic values, which tie photosymbiosis to major cora

299 disposed to different ecological strategies (symbiotic versus free-living lifestyles) depending on th

300 In essence, she presented a comprehensive symbiotic view of eukaryotic cell evolution (eukaryogene