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

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

4 Cyanobacterial aldehyde decarbonylase (cAD) is a non-hem

5 Cyanobacterial aldehyde-deformylating oxygenase (cADO) c

6 Cyanobacterial aldehyde-deformylating oxygenases (ADOs)

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

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

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

10 en a plastid-encoded RNA polymerase (PEP) of cyanobacterial ancestry and a nucleus-encoded RNA polyme

11 per 1.5 cm thick sediment had 7.2 times more cyanobacterial and 1.7 times more diatom rRNA sequences

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

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

14 Cyanobacterial and glaucophyte FtsZ properties mostly re

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

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

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

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

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

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

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

22 mirroring an early step in the biogenesis of cyanobacterial beta-carboxysomes.

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

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

25 We caused a cyanobacterial bloom by gradually enriching an experimen

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

27 Nutrient-cyanobacterial bloom interactions were examined in eutro

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

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

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

31 methods/approaches are being used to monitor cyanobacterial blooms and detect microcystins in freshwa

32 Annual cyanobacterial blooms dominated by Microcystis have occu

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

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

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

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

37 Cyanobacterial blooms in western Lake Erie have recently

38 Although toxic cyanobacterial blooms in western Lake Erie threaten drin

39 itable monitoring approaches to characterize cyanobacterial blooms is an important goal.

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

41 Cyanobacterial blooms often occur in freshwater lakes an

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

43 Cyanobacterial blooms, dominated by Microcystis sp. and

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

45 monitoring approaches that are applicable to cyanobacterial blooms, especially those that focus on th

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

47 ed with the challenging task of dealing with cyanobacterial blooms.

48 anges in the genotype composition of harmful cyanobacterial blooms.

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

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

51 Bioengineering a cyanobacterial carbon-concentrating mechanism (CCM) into

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

53 The cyanobacterial carboxysome is a proteinaceous microcompa

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

55 s developed to examine how components of the cyanobacterial CCM affect leaf light-saturated CO(2) upt

56 The cyanobacterial CCM is an attractive alternative relative

57 We present a mathematical model of the cyanobacterial CCM, giving the parameter regime (express

58 addition of the remaining components of the cyanobacterial CCM, such as inorganic carbon transporter

59 soform would perform better in a leaf with a cyanobacterial CCM.

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

61 mographic tilt series of cyanophage-infected cyanobacterial cells embedded in ice, without staining o

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

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

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

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

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

67 they are crucial for phototrophic growth of cyanobacterial cells, biogenesis of thylakoid membranes

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

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

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

71 erimental data on oxygen production rates of cyanobacterial cells.

72 mension to the intracellular organization in cyanobacterial cells.

73 tructural flexibility in the architecture of cyanobacterial cells.

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

75 We first prepared cyanobacterial ChlB variants with amino acid substitutio

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

77 The cyanobacterial circadian clock consists of a post-transl

78 We show that the cyanobacterial circadian clock generates a rhythm in met

79 The cyanobacterial circadian clock generates genome-wide tra

80 The cyanobacterial circadian clock system has been extensive

81 In the model cyanobacterial circadian clock system, the core oscillat

82 The cyanobacterial circadian pacemaker consists of a three-p

83 The cyanobacterial circadian program exerts genome-wide cont

84 Moreover, the cyanobacterial circadian program regulates gene activity

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

86 This work shows that the cyanobacterial circadian system undergoes a circadian or

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

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

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

90 n oscillations are generated by the purified cyanobacterial clock proteins, KaiA, KaiB, and KaiC, thr

91 onary advantage of integrating CikA into the cyanobacterial clock, challenge the conventional constru

92 Engineering the cyanobacterial CO2 -concentrating mechanism, the carboxy

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

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

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

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

97 Cyanobacterial community composition fluctuated dynamica

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

99 The cyanobacterial community constituted close to 12% of the

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

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

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

103 three-dimensional structure of the canonical cyanobacterial CP12 in complex with GAPDH suggests that

104 Furthermore, modeling of the cyanobacterial CP12 protein variants based on the recent

105 reveals a heretofore unobserved diversity in cyanobacterial CP12 proteins.

106 H suggests that some of the newly identified cyanobacterial CP12 types are unlikely to bind to GAPDH.

107 aches have been applied to the analysis of a cyanobacterial culture and a natural bloom, and MC equiv

108 Results for algal/cyanobacterial cultures (n = 12) and seawater samples (n

109 d phycobiliproteins causes a color change of cyanobacterial cultures from blue-green to yellow-green,

110 Cyanobacterial cultures in particular can generate a lar

111 various matrices, including drinking water, cyanobacterial cultures, extracts, and algal blooms, and

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

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

114 The cyanobacterial cytochrome b(6)f complex is central for t

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

116 tensities and produces less O(2) than either cyanobacterial D1 isoform.

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

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

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

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

121 uenced to oligotrophic waters did not detect cyanobacterial diazotrophs commonly found in other open

122 st 10 years, crystal structures of a 700 kDa cyanobacterial dimeric PSII complex have been reported w

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

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

125 l-characterized family of split inteins, the cyanobacterial DnaE inteins, show particular promise, as

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

127 ng either of these gene organizations infect cyanobacterial ecotypes biogeographically restricted to

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

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

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

131 Remarkably, both the plant and cyanobacterial enzymes have evolved through convergent e

132 genes for photosynthesis relatively late in cyanobacterial evolution.

133 Cyanobacterial FDPs constitute a specific protein group

134 Evolution of unique cyanobacterial FDPs is discussed as a prerequisite for t

135 Cyanobacterial flavodiiron proteins (FDPs; A-type flavop

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

137 microbiological investigations suggested the cyanobacterial genera Synechococcus and Aphanizomenon as

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

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

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

141 obacterium into the eukaryotic plastid, most cyanobacterial genes were transferred to the nucleus or

142 the amount and the phylogenetic diversity of cyanobacterial genome sequence data.

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

144 Furthermore, CcmP and its orthologs in alpha-cyanobacterial genomes form a distinct clade of shell pr

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

146 al protein (dubbed CcmP) encoded in all beta-cyanobacterial genomes is part of the carboxysome.

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

148 each distributed among taxonomically diverse cyanobacterial genomes.

149 We found that six distinct clusters of cyanobacterial genotypes are distributed throughout the

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

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

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

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

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

155 ould significantly improve the robustness of cyanobacterial growth against bacterial contamination.

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

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

158 genetic and environmental factors regulating cyanobacterial growth.

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

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

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

162 Cyanobacterial harmful algal blooms (CyanoHABs) have ser

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

164 ved domain was essential for Arabidopsis and cyanobacterial HDR function.

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

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

167 Cyanobacterial hli genes are high-light induced and requ

168 Regulation 5 to safeguard photosystem I, the cyanobacterial homolog of Proton Gradient Regulation 5 i

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

170 The cyanobacterial host also has two complete CRISPR (cluste

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

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

173 stem constitutes a key output pathway of the cyanobacterial Kai circadian oscillator.

174 Cyanovirin-N (CVN), a cyanobacterial lectin, exemplifies a class of antiviral

175 Cyanobacterial light sensing may have been facilitated b

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

177 We estimated divergence times of extant cyanobacterial lineages under Bayesian relaxed clocks fo

178 tle is known about the temporal evolution of cyanobacterial lineages, and possible interplay between

179 An operon encoding PSI was identified in cyanobacterial marine viruses.

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

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

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

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

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

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

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

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

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

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

190 al phytochrome2 (Cph2), a phytochrome of the cyanobacterial model system Synechocystis sp. PCC 6803,

191 Cell lysates of the cyanobacterial mutants further functionalized recombinan

192 Plant and cyanobacterial mutants in ycf54 display impaired functio

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

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

195 amed NdhP) represents a novel subunit of the cyanobacterial NDH1 complex, mediating its coupling eith

196 ng of the structure-function relation of the cyanobacterial NDH1 complex, the subunits catalyzing NAD

197 It is generally accepted that cyanobacterial NiFe-hydrogenases are reduced by NAD(P)H.

198 udy asserts that a late evolutionary leap in cyanobacterial nitrogen fixation terminated a long histo

199 In cyanobacterial Nostoc species, substratum-dependent glid

200 idences the immediately post-GOE presence of cyanobacterial nostocaceans characterized by specialized

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

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

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

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

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

206 de insight into the distribution of genes of cyanobacterial origin in eukaryotic nuclear genomes.

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

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

209 The cyanobacterial pacemaker is a posttranslational regulati

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

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

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

213 A cyanobacterial pathway consisting of acyl-Acyl Carrier P

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

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

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

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

218 ally modular photoactive protein involved in cyanobacterial photoprotection.

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

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

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

222 er similar to that observed by Liu et al. in cyanobacterial Photosystem II.

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

224 The cyanobacterial phylum encompasses oxygenic photosyntheti

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

226 nd appears to be widely conserved within the cyanobacterial phylum.

227 of IsaR1 are widely conserved throughout the cyanobacterial phylum.

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

229 s, the reverse process (Pr formation) in the cyanobacterial phytochrome was slower by a factor of thr

230 Here, we describe a function of cyanobacterial phytochrome2 (Cph2), a phytochrome of the

231 gher in heterotrophic bacteria compared with cyanobacterial phytoplankton.

232 genes involved in nitrogen assimilation, the cyanobacterial PII-interacting protein X (PipX) interact

233 ne the role of genes potentially involved in cyanobacterial plastoquinone biosynthesis, we have focus

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

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

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

237 As natural cyanobacterial populations include producing and non-pro

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

239 rmine the degree of recombination within the cyanobacterial populations.

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

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

242 The cyanobacterial prenyltransferase AmbP3 catalyzes the rev

243 prevalent, yet medicinally underappreciated, cyanobacterial protease inhibitor scaffold and undertook

244 show that IM30, a conserved chloroplast and cyanobacterial protein of approximately 30 kDa binds as

245 ome sequencing, identifying more than 21,000 cyanobacterial proteins with no detectable similarity to

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

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

248 Mn4CaO5 water-oxidizing complex (WOC) within cyanobacterial PSII.

249 Cyanobacterial regulation of gene expression must conten

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

251 L protein is part of a complex essential for cyanobacterial respiration.

252 We studied the photocurrents of a cyanobacterial rhodopsin Gloeobacter violaceus (GR) in X

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

254 Cyanobacterial Rubisco enzymes are faster than those of

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

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

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

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

259 6-fold increase in the relative abundance of cyanobacterial sequences and a dramatic die-off of algae

260 Among cyanobacterial sequences, the proportion of sequences be

261 However, cyanobacterial Sfp-type PPTases remain poorly characteri

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

263 We apply our method to a dataset of 11 cyanobacterial species and demonstrate the large impact

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

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

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

267 Recently, a deep-branching cyanobacterial species, Candidatus Gloeomargarita lithop

268 lization is not dependent on other clock- or cyanobacterial-specific factors.

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

270 17 specific antibodies to the most frequent cyanobacterial strains blooming in freshwater ecosystems

271 intracellular Ca-carbonate inclusions in 68 cyanobacterial strains distributed throughout the phylog

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

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

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

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

276 ribozyme-based insulator in several diverse cyanobacterial strains.

277 he structure of this core differs in diverse cyanobacterial strains.

278 phylogenetically and phenotypically diverse cyanobacterial strains.

279 carotenoid protein (OCP), is present in most cyanobacterial strains; it is activated by high light co

280 Which sugars and cyanobacterial sugar uptake mechanism(s) are involved in

281 Cyanobacterial symbionts cultured from sponges were show

282 The most abundant cyanobacterial symbionts form heterocysts (specialized c

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

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

285 isingly high numbers in all prokaryotes, but cyanobacterial TA systems have been only very poorly exp

286 We discovered that diverse unicellular cyanobacterial taxa form intracellular amorphous Ca-carb

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

288 itions, indicating that the newly discovered cyanobacterial TCA cycle (via the gamma-aminobutyric aci

289 The cyanobacterial thylakoid membrane represents a model mem

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

291 Knowledge of cyanobacterial thylakoid membranes could also be extende

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

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

294 (CYN), a widely distributed and highly toxic cyanobacterial toxin (cyanotoxin), remains poorly elucid

295 etection of five groups of harmful algal and cyanobacterial toxins found in marine, brackish, and fre

296 wed high specificity toward other coexistent cyanobacterial toxins of microcystin-LR and Anatoxin-a.

297 As anticipated, the cyanobacterial transcriptome exhibited pronounced diel p

298 rate dehydrogenase complex is missing in the cyanobacterial tricarboxylic acid cycle.

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

300 Here we report a 4.7-A structure of a cyanobacterial virus, Syn5, by electron cryo-microscopy