ライフサイエンスコーパス: cyanobacterial

1 has not been definitively established, but a cyanobacterial [2Fe-2S] ferredoxin (PetF), reduced by fe

2 ic) on total phytoplankton chlorophyll-a and cyanobacterial abundance and composition.

3 he third hypotheses: total phytoplankton and cyanobacterial abundance increased in heated mesocosms w

4 s; (b) the stimulatory effects of warming on cyanobacterial abundance would be enhanced in higher nut

5 heses were that: (a) total phytoplankton and cyanobacterial abundance would be higher in heated mesoc

6 Here, we assess shifts in cyanobacterial abundances and global gene-expression pat

7 Our insights into quantitative aspects of cyanobacterial acclimations to different growth rates ha

8 isticated genetic mechanisms are involved in cyanobacterial adaptation to the extreme environment of

9 Cyanobacterial aldehyde-deformylating oxygenase (cADO) c

10 Furthermore we show that cyanobacterial alkane production is likely sufficient to

11 e hydrocarbon-degrading bacteria can consume cyanobacterial alkanes, which likely prevents these hydr

12 Cyanobacterial alternative sigma factors are crucial pla

13 c eukaryotes acquired KDPG aldolase from the cyanobacterial ancestors of plastids via endosymbiotic g

14 rd understanding the molecular components of cyanobacterial and algal CCMs, as well as recent advance

15 tabolites from an in-house library of marine cyanobacterial and algal collections.

16 olecular clock analyses, including data from cyanobacterial and chloroplast genomes using a Bayesian

17 Cyanobacterial and glaucophyte FtsZ properties mostly re

18 GVs can be isolated from natural cyanobacterial and haloarchaeal host organisms or from E

19 erence in the chloride-binding properties of cyanobacterial and higher-plant PSII.

20 d by swapping enzymes from distantly related cyanobacterial and Pseudomonas species.

21 ifferent types of biosynthetic pathways from cyanobacterial and Streptomyces strains.

22 ant insight into the molecular mechanisms of cyanobacterial and vertebrate animal clocks.

23 interacts with the phycobilisome (PBS), the cyanobacterial antenna, and induces excitation-energy qu

24 P(r)) is able to bind to phycobilisomes, the cyanobacterial antenna, and to quench excess energy.

25 at the level of the phycobilisome (PBS), the cyanobacterial antenna, induced by the orange carotenoid

26 variants correlated with different groups of cyanobacterial ASVs including time-lagged predator-prey

27 ry metabolites, an impressive four times the cyanobacterial average.

28 ck grama grassland suffered severe losses in cyanobacterial biomass and diversity, but compositionall

29 lex extracts of MC producing or nonproducing cyanobacterial biomasses, and of a Microcystis aeruginos

30 We caused a cyanobacterial bloom by gradually enriching an experimen

31 Intensified cyanobacterial bloom events are of increasing global con

32 ration and load thresholds needed to control cyanobacterial bloom formation.

33 to this system as N may significantly impact cyanobacterial bloom size and toxicity.

34 ially derived secondary metabolites during a cyanobacterial bloom that emerged in a highly urbanized

35 concentrations were depleted during a dense cyanobacterial bloom, but were replaced by strains with

36 e summer of 2015 during the development of a cyanobacterial bloom.

37 The global expansion of harmful cyanobacterial blooms (CyanoHABs) poses an increasing th

38 to mitigate increasing incidences of harmful cyanobacterial blooms (CyanoHABs), but little attention

39 Harmful cyanobacterial blooms (HCBs) are becoming a major challe

40 Cyanobacterial blooms are an increasing threat to water

41 ange is an impressive factor with effects on cyanobacterial blooms as source of microcystins.

42 stin, a known hepatotoxin and a byproduct of cyanobacterial blooms can be a risk factor for NAFLD ass

43 Annual cyanobacterial blooms dominated by Microcystis have occu

44 Sandusky Bay experiences annual toxic cyanobacterial blooms dominated by Planktothrix agardhii

45 is, a notorious genus that can develop toxic cyanobacterial blooms in many eutrophic lakes and reserv

46 eria, thereby preventing the reoccurrence of cyanobacterial blooms in the following summer.

47 one may not significantly reduce the risk of cyanobacterial blooms in western Lake Erie but rather ma

48 Although toxic cyanobacterial blooms in western Lake Erie threaten drin

49 eshwater bacterial community associated with cyanobacterial blooms is largely conserved at the phylum

50 Cyanobacterial blooms often occur in freshwater lakes an

51 Cyanobacterial blooms produce hazardous toxins, deplete

52 ent has led to dramatic increases in harmful cyanobacterial blooms, creating serious threats to drink

53 contributed to severe and recurring harmful cyanobacterial blooms, especially by the non-N(2) -fixin

54 kton communities can be strongly affected by cyanobacterial blooms, especially species of genus Daphn

55 anges in the genotype composition of harmful cyanobacterial blooms.

56 e hydrolysis of polysaccharides, likely from cyanobacterial blooms.

57 crocystin, a group of toxins associated with cyanobacterial blooms.

58 sessments of the N(2) fixation efficiency of cyanobacterial blooms.

59 The carboxysome, the cyanobacterial BMC for CO(2) fixation, has attracted sig

60 d be exploited to increase the efficiency of cyanobacterial carbon metabolism and photosynthetic prod

61 his complex is embedded and functions in the cyanobacterial carbon-concentrating mechanism.

62 cted a synthetic mimic of the carboxysome, a cyanobacterial carbon-fixing organelle.

63 The cyanobacterial carboxysome is a proteinaceous microcompa

64 ocalized CO2 fixation in C4 plants or in the cyanobacterial carboxysome, enhances the activity of ine

65 s part of ongoing efforts to engineer a beta-cyanobacterial CCM into land plants, we investigated the

66 filament-forming CCRPs and demonstrate that cyanobacterial CCRPs are involved in cell morphology, mo

67 The organization of the cyanobacterial cell revealed here substantially aids our

68 ensive subcellular proteome map of an entire cyanobacterial cell, identifying ~67% of proteins in Syn

69 s tied to thylakoid rigidity in this type of cyanobacterial cell.

70 nes current research on the incorporation of cyanobacterial cells and cyanotoxins into SA of aquatic

71 The structural organization of cyanobacterial cells and the arrangement of the thylakoi

72 l metabolite production in photoautotrophic, cyanobacterial cells is a desirable venture.

73 The photosynthetic machinery in cyanobacterial cells is housed in flattened membrane str

74 However, localization of proteins within cyanobacterial cells is poorly understood.

75 However, it is not known how cyanobacterial cells limit O(2) diffusion across their m

76 iophotovoltaic cell consisting of a layer of cyanobacterial cells on top of a carbon nanotube conduct

77 dynamics of individual wild-type and mutant cyanobacterial cells over multiple generations.

78 tions predict robust oscillations in modeled cyanobacterial cells provided that thylakoid network per

79 DeltandhR mutant successfully preacclimates cyanobacterial cells to lowered Ci supply under HC condi

80 microscopy platform that allows us to expose cyanobacterial cells to pulses of light and dark while q

81 ecular processes that involve the ability of cyanobacterial cells to sense ambient light colors and u

82 Certain unicellular cyanobacterial cells, such as Cyanothece sp. ATCC 51142,

83 omes are vital to the CO2-fixing activity of cyanobacterial cells.

84 cesses such as nitrogen fixation to occur in cyanobacterial cells.

85 ene transfer extends beyond hosts to nonhost cyanobacterial cells.

86 ubisco, prior transgenic plants included the cyanobacterial chaperone RbcX or the carboxysomal protei

87 hic bacteria will need to be revised for the cyanobacterial chassis.

88 We first prepared cyanobacterial ChlB variants with amino acid substitutio

89 ecently discovered third group consisting of cyanobacterial chloride and sulfate ion-pumping rhodopsi

90 eport experimental platforms for driving the cyanobacterial circadian clock both in vivo and in vitro

91 malian cells and simplify the entrainment of cyanobacterial circadian rhythm.

92 However, contributions of some cyanobacterial clades were proportionally relatively con

93 ic phasing to the dynamical structure of the cyanobacterial clock as an oscillator and explored the p

94 Early research on the cyanobacterial clock focused on characterizing the genes

95 xysomes, bacterial organelles central to the cyanobacterial CO2 concentrating mechanism.

96 Cyanotoxins obtained from a freshwater cyanobacterial collection at Green Lake, Seattle during

97 dients in soluble reactive phosphorus shaped cyanobacterial communities and elicited the largest tran

98 h P scavenging (pstSCAB, phoX) and dominated cyanobacterial communities.

99 anted to better understand how the algal and cyanobacterial community changed throughout an open wate

100 Cyanobacterial community composition fluctuated dynamica

101 N, phosphorus (P) or both N and P may alter cyanobacterial community composition.

102 The cyanobacterial community constituted close to 12% of the

103 e community structure more strongly explains cyanobacterial community structure at the ASV level than

104 ly, water temperature is a primary driver of cyanobacterial community succession, with warming favour

105 n Lake Erie in 2014, we investigated how the cyanobacterial community varied over space and time, and

106 of reliable synthetic biology tools for the cyanobacterial community.

107 cipitation were major parameters determining cyanobacterial composition, suggesting the presence of d

108 al extracts from Padina and Ulva species and cyanobacterial compounds antillatoxin B, laxaphycins A,

109 photonic system for in situ detection of low cyanobacterial concentrations in water samples.

110 e first time CRISPRs have been reported in a cyanobacterial/cyanophage system.

111 t also of ycf54; conversely, coexpression of cyanobacterial cycI and ycf54 is required to complement

112 sothermal titration calorimetry performed at cyanobacterial cytosol or meaningful environmental pHs v

113 Substitution of cyanobacterial D1-Asn87 by higher-plant D1-Ala87 is the

114 in the same defects as those observed in the cyanobacterial demethylnaphthoquinone methyltransferase

115 The unicellular cyanobacterial diazotroph UCYN-A was detected from seawa

116 erstanding the evolution of the free-living, cyanobacterial, diazotroph Trichodesmium is of great imp

117 Cyanobacterial diazotrophs are considered to be the most

118 d layers and a homogeneous water column, non-cyanobacterial diazotrophs belonging mainly to nifH clus

119 therefore explain how non-heterocyst-forming cyanobacterial diazotrophs can fix N(2) in the fully oxi

120 llular cyanobacteria, subcluster 1B) and non-cyanobacterial diazotrophs from clusters 1G and 3.

121 und that, whereas all non-heterocyst-forming cyanobacterial diazotrophs had hopanoid synthesis genes,

122 a conserved trait in non-heterocyst-forming cyanobacterial diazotrophs that might lower the permeabi

123 America coastal waters, driven primarily by cyanobacterial diazotrophs.

124 Our study enhances understanding of cyanobacterial distributions in an ecologically importan

125 stoichiometric and energetic constraints of cyanobacterial diurnal growth is limited.

126 exist regarding the composition of biocrust cyanobacterial diversity and distribution in Mediterrane

127 We describe cyanobacterial diversity in Mediterranean semiarid soil

128 ses (1-3 mg N L(-1) week(-1)) promoted toxic cyanobacterial dominance and elevated concentrations of

129 ng future N pollution will help curb further cyanobacterial dominance in lakes both directly and by c

130 ion regimes in P-rich lakes will favor toxic cyanobacterial dominance, restricting future N pollution

131 nalyses, and detect clear shifts along it in cyanobacterial dominance.

132 l Gene Transfer (HGT) event, probably from a cyanobacterial donor species.

133 may have irrevocably cleared self-sustaining cyanobacterial ecosystems, thereby creating the ecologic

134 otes, and the independent incorporation of a cyanobacterial endosymbiont by Paulinella Our analyses i

135 Primary plastids descend from the cyanobacterial endosymbiont of an ancient eukaryotic hos

136 ancestral orthologous gene families from the cyanobacterial endosymbiont remained in chromatophore DN

137 f these proteins, derived from the ancestral cyanobacterial endosymbiont that gave rise to plastids.

138 Chloroplasts evolved from a cyanobacterial endosymbiont that resided within a eukary

139 Furthermore, Ado/Aar and the non-cyanobacterial enzymes UndA and fatty acid photodecarbox

140 genes for photosynthesis relatively late in cyanobacterial evolution.

141 rinus, revealed high levels of similarity to cyanobacterial Fds (root mean square deviations of <=0.5

142 he high levels of structural similarity with cyanobacterial Fds and reactivity with a host sulfite re

143 d that phage Fds are most closely related to cyanobacterial Fds that transfer electrons from photosys

144 The gene encoding the cyanobacterial ferritin SynFtn is up-regulated in respon

145 Comparison of atomistic models of a native cyanobacterial form (Thermosynechococcus vulcanus) and a

146 microbiological investigations suggested the cyanobacterial genera Synechococcus and Aphanizomenon as

147 d in the gene-dense genomes of the sympatric cyanobacterial genera Synechococcus and Prochlorococcus,

148 disease, has been identified in more than 20 cyanobacterial genera.

149 Although the movement of cyanobacterial genes from endosymbiont to host is well s

150 s have been proposed to arise from ancestral cyanobacterial genes via endosymbiotic gene transfer (EG

151 Cyanobacterial genomes encode several isoforms of the D1

152 ng motif was retained in all currently known cyanobacterial genomes except for a single lineage of en

153 bioinformatic searches of over 100 sequenced cyanobacterial genomes for B12 biosynthesis genes, inclu

154 Surveying cyanobacterial genomes for coiled-coil-rich proteins (CC

155 The increasing availability of cyanobacterial genomes has enabled the identification of

156 ng both plastocyanin and Cyt c6 in algal and cyanobacterial genomes might be because plastocyanin pro

157 As cyanobacterial genomes typically encode multiple sigma f

158 With the increasing availability of cyanobacterial genomes, bioinformatic analysis has revea

159 each distributed among taxonomically diverse cyanobacterial genomes.

160 on to examine the microdiversity within this cyanobacterial genus during these blooms as well as furt

161 Chemical investigations of the cyanobacterial genus Moorea have resulted in the isolati

162 The best examples are the cyanobacterial genus Prochlorococcus, the alphaproteobac

163 isolation of the bartolosides, unprecedented cyanobacterial glycolipids featuring aliphatic chains wi

164 ive relationships between the occurrences of cyanobacterial groups and off-flavor compounds (2-methyi

165 carbon-to-phosphorus ratios than single cell cyanobacterial groups, with the exception of one group o

166 o greenhouse gas emission scenarios, and two cyanobacterial growth scenarios, is unique in coupling c

167 f an intact shell and cargo is essential for cyanobacterial growth under ambient CO(2) concentrations

168 s bioreactors that trigger rapid and massive cyanobacterial growth with remarkable economic and healt

169 N chemical speciation influences cyanobacterial growth, persistence and the production of

170 llution of eutrophic lakes can promote toxic cyanobacterial growth, some cases of extreme N loading h

171 genetic and environmental factors regulating cyanobacterial growth.

172 uture P loading and climate warming to drive cyanobacterial growth.

173 rmine the porphyrin-docking mechanism to the cyanobacterial Gun4 structure.

174 l collection at Green Lake, Seattle during a cyanobacterial harmful algal bloom in the summer of 2014

175 vities are causing a global proliferation of cyanobacterial harmful algal blooms (CHABs), yet we have

176 Cyanobacterial harmful algal blooms (cyanoHABs) are a se

177 Cyanobacterial harmful algal blooms (CyanoHABs) have ser

178 f by increased frequencies and magnitudes of cyanobacterial harmful algal blooms (CyanoHABs) in fresh

179 n of a VHH phage display library against the cyanobacterial hepatotoxin microcystin LR and its select

180 Microcystins are a major group of cyanobacterial heptapeptide toxins found in freshwater a

181 proteins, and the pigment-binding ability of cyanobacterial high-light-inducible proteins has been st

182 Cyanobacterial hli genes are high-light induced and requ

183 nching, and the one-helix proteins and their cyanobacterial homologs designated high-light-inducible

184 Using thermophilic cyanobacterial homologs, we solve crystal structures of

185 The cyanobacterial host also has two complete CRISPR (cluste

186 The cyanobacterial host contains a CRISPR-Cas system with CR

187 waters [5-7] and frequently outnumber their cyanobacterial hosts [8].

188 Cyanobacterial Hox is a [NiFe] hydrogenase that consists

189 None of the algal extracts or cyanobacterial isolates had antibacterial activity again

190 structure in which a concentric filamentous cyanobacterial layer encloses noncyanobacterial aggregat

191 Here, we port a cyanobacterial light sensor pathway comprising the green

192 its closet relative Gloeomargarita, a basal cyanobacterial lineage, approximately 2.1 billion y ago

193 plored all known genomes of the major marine cyanobacterial lineages for the presence of hopanoid syn

194 P. paru and S. iseri, and found that benthic cyanobacterial mats comprised 36.7% +/- 5.8% and 15.0% +

195 tatranscriptomic sequencing was conducted on cyanobacterial mats of the Middle Island Sinkhole (MIS),

196 ly undocumented, top-down control on benthic cyanobacterial mats on Caribbean reefs.

197 Tang (Acanthurus coeruleus) consume benthic cyanobacterial mats on coral reefs in Bonaire, Netherlan

198 of its ability to control coral reef benthic cyanobacterial mats, which have recently proliferated on

199 on in Hamelin Pool are formed by filamentous cyanobacterial mats.

200 All cyanobacterial membranes contain diesel-range C15-C19 hy

201 network renders the rational engineering of cyanobacterial metabolism for the generation of biomass,

202 cyanobacteria and it plays a pivotal role in cyanobacterial metabolism.

203 themselves that converted otherwise unusable cyanobacterial metabolites into host energy stores.

204 We review current information about cyanobacterial microcompartments and carbon-concentratin

205 ed for water toxicity estimation in terms of cyanobacterial microcystin toxins (MCs) detection.

206 port here a generic noncompetitive assay for cyanobacterial microcystins (MCs) and nodularins (Nod),

207 tion as a hypothetical Mn transporter in the cyanobacterial model strain Synechocystis sp PCC 6803 an

208 Cell lysates of the cyanobacterial mutants further functionalized recombinan

209 Plant and cyanobacterial mutants in ycf54 display impaired functio

210 has been paid on the roles and importance of cyanobacterial N(2)-fixation and phosphorus (P) scavengi

211 The highly active cyanobacterial N(2)-fixers were dominated by Nostoc and

212 PPTases and provide new tools to synthesize cyanobacterial natural products using in vitro and in vi

213 and time, and whether the bloom affected non-cyanobacterial (nc-bacterial) diversity and composition.

214 the bacterial 16S rRNA V3-V4 region and the cyanobacterial ntcA gene.

215 terminal POTRA domains, three in the case of cyanobacterial Omp85.

216 yanobacterium-derived domain fused to one of cyanobacterial or another prokaryotic origin and have em

217 relevant pathway combining genes with host, cyanobacterial or bacterial ancestry, but we detect no s

218 ycoerythrin and orange carotenoid protein of cyanobacterial origin are significantly greater in orang

219 thyisoborneol and beta-ionone), suggesting a cyanobacterial origin.

220 gelatinosus rescues the loss not only of its cyanobacterial ortholog, cycI, in Synechocystis sp. PCC

221 sample of genes from the proteobacterial and cyanobacterial pangenomes of their respective day and th

222 ially became enriched including the putative Cyanobacterial PAOs Obscuribacterales and Leptolyngbya a

223 and low-light acclimation in the underlying cyanobacterial part.

224 in vivo absorption signatures of diatom and cyanobacterial photopigments, which were confirmed by HP

225 In cyanobacterial photoprotection, the orange carotenoid pr

226 CP) is known as an effector and regulator of cyanobacterial photoprotection.

227 ific roles of the COCP carotenoid carrier in cyanobacterial photoprotection.

228 ally modular photoactive protein involved in cyanobacterial photoprotection.

229 ange Carotenoid Protein (OCP) is involved in cyanobacterial photoprotection.

230 resulting bilin was incorporated into model cyanobacterial photoreceptors and into phytochrome from

231 rigin, variable among mats, originating from cyanobacterial photosynthate.

232 levels of oxygen as a byproduct of blooming cyanobacterial photosynthesis resulted in a redox upshif

233 ional genes, including those associated with cyanobacterial photosynthesis, secondary metabolism and

234 , responsible for the photoprotection of the cyanobacterial photosynthetic apparatus under excessive

235 Cyanobacterial photosystem I (PSI) functions as a light-

236 elf-assembles to form the midantenna rods of cyanobacterial phycobilisomes.

237 NsiR4 is widely conserved throughout the cyanobacterial phylum, suggesting a conserved function.

238 of IsaR1 are widely conserved throughout the cyanobacterial phylum.

239 model that is quantitatively consistent with cyanobacterial physiology, emphasizing that pH cannot be

240 gher in heterotrophic bacteria compared with cyanobacterial phytoplankton.

241 nts for fluorescence measurement of specific cyanobacterial pigments, that is, phycocyanin.

242 ioning in vitro as a shuttle among different cyanobacterial pools of reducing equivalents.

243 Deep sequencing of a thermophilic cyanobacterial population and analysis of the statistics

244 The Synechococcus cyanobacterial population at the Scripps Institution of

245 Overall, the pre-bloom cyanobacterial population was more genetically diverse,

246 ke Erie but rather may promote a shift among cyanobacterial populations (Microcystis, Anabaena, and P

247 As natural cyanobacterial populations include producing and non-pro

248 Anabaena and Planktothrix were the dominant cyanobacterial populations, and experimental P and ammon

249 Here we report crystal structures of cyanobacterial PORs from Thermosynechococcus elongatus a

250 s reveal the versatile catalysis of selected cyanobacterial PPTases and provide new tools to synthesi

251 e of Synechocystis sp. PCC6803, two selected cyanobacterial PPTases and Sfp supported the growth of r

252 The cyanobacterial prenyltransferase AmbP3 catalyzes the rev

253 nonphotochemical quenching may not increase cyanobacterial productivity in PBRs with rapidly changin

254 acteria, a homologous protein (activase-like cyanobacterial protein, ALC), contains a distinctive C-t

255 roduced with and without the RbcX and CcmM35 cyanobacterial proteins.

256 ed plastids (termed chromatophores) of alpha-cyanobacterial provenance.

257 n intermediate evolutionary link between the cyanobacterial PSI reaction center and its green algal/h

258 Cyanobacterial regulation of gene expression must conten

259 nzyme supports a vertical inheritance from a cyanobacterial-related ancestor.

260 Using cyanobacterial RNAP as a model, we investigated alternat

261 We suggest that cyanobacterial RNAP has a specific Trigger Loop domain c

262 Features of the cyanobacterial RNAP hydrolysis are reminiscent of the Gr

263 lacement of Rubisco in a model C3 plant with cyanobacterial Rubisco and progress toward synthesizing

264 Cyanobacterial Rubisco enzymes are faster than those of

265 ulatory sequences on the Rubisco transgenes, cyanobacterial Rubisco expression was enhanced and the t

266 minal beta-hairpin renders the assembly of a cyanobacterial Rubisco independent of RbcX.

267 Although cyanobacterial rubisco is believed to be less sensitive

268 actors may not be adequate for assembly of a cyanobacterial Rubisco, prior transgenic plants included

269 nor CcmM35 is needed for assembly of active cyanobacterial Rubisco.

270 However, cyanobacterial Sfp-type PPTases remain poorly characteri

271 be the detailed characterization of multiple cyanobacterial Sfp-type PPTases that were rationally sel

272 he genomic context of putative regulators of cyanobacterial sigma factors.

273 ether Chl f is synthesized from Chl a in the cyanobacterial species Halomicronema hongdechloris.

274 oprim, tylosin, and lincomycin) to algal and cyanobacterial species in European surface waters.

275 Actinobacteria as the main taxa despite the cyanobacterial species present and geographical (Asia, E

276 in, orthologs of which are found in multiple cyanobacterial strains as well as chloroplasts of higher

277 17 specific antibodies to the most frequent cyanobacterial strains blooming in freshwater ecosystems

278 Comparisons against more established cyanobacterial strains identified a number of difference

279 Many cyanobacterial strains synthesize sucrose as an osmoprot

280 (Ca), strontium (Sr), and barium (Ba) by two cyanobacterial strains, Cyanothece sp. PCC7425 and Gloeo

281 At least 30 cyanobacterial strains, most of which are known to have

282 In most nitrogen-fixing cyanobacterial strains, there are one to four paralogous

283 open new avenues in engineering programs of cyanobacterial strains.

284 microbiota remained relatively stable during cyanobacterial symbiont acquisition at both structural (

285 first evidence of horizontal acquisition of cyanobacterial symbionts by a marine sponge.

286 Cyanobacterial symbionts cultured from sponges were show

287 N(2)-fixing cyanobacterial symbioses are widespread in the oceans, e

288 unlit zones of aquatic environments, diverse cyanobacterial symbioses exist with autotrophic taxa in

289 hat the protein adopts a similar fold as the cyanobacterial T-type lyase CpcT from Nostoc sp. PCC7120

290 a putative phycobiliprotein lyase related to cyanobacterial T-type lyases, which facilitate attachmen

291 explained by the differential sensitivity of cyanobacterial taxa: nitrogen-fixing Scytonema spp. were

292 The cyanobacterial thylakoid membrane represents a model mem

293 tis sp. PCC 6803 assessed the flexibility of cyanobacterial thylakoid membrane sheets and the depende

294 Knowledge of cyanobacterial thylakoid membranes could also be extende

295 mportance, the native organization of PSI in cyanobacterial thylakoid membranes is poorly understood.

296 iversal role of medium-chain hydrocarbons in cyanobacterial thylakoid membranes: they regulate redox

297 Cyanobacterial TM protein localization was conserved in

298 s N loads required to shift communities from cyanobacterial to chlorophyte dominance are unclear, we

299 r thermal reversion, that assembled with the cyanobacterial version phycocyanobilin, often used for o

300 We show sometimes >50% of all cyanobacterial+viral psbA expression is of viral origin,