ライフサイエンスコーパス: cyanobacteria

1 ) carotenoid and mediates photoprotection in cyanobacteria.

2 iles and alka/enes not naturally produced by cyanobacteria.

3 cting, and perhaps lysogenizing, filamentous cyanobacteria.

4 ns for improved yield from plants, algae and cyanobacteria.

5 d oomycetes to testate amoebozoans, and even cyanobacteria.

6 novel types of CO(2)-derived hydrocarbons in cyanobacteria.

7 NPQ) of the light-harvesting process in most cyanobacteria.

8 ntation products of metabolically engineered cyanobacteria.

9 tolerant, novel phylotypes of bundle-forming cyanobacteria.

10 differentiated climatic niches for distinct cyanobacteria.

11 was likely linked to the origins of oxygenic Cyanobacteria.

12 ellular resistance in the marine unicellular cyanobacteria.

13 n systems prone to contamination by invasive cyanobacteria.

14 -inducible protein early in the evolution of cyanobacteria.

15 a cryptic c-type heme protein widespread in cyanobacteria.

16 ws fast, sensitive, and in situ detection of cyanobacteria.

17 al blooms that often contain toxin-producing cyanobacteria.

18 protein that governs photoprotection in many cyanobacteria.

19 ch some are thermo-epilithic biofilm-forming cyanobacteria.

20 sity, and spatial distribution of Baltic Sea cyanobacteria.

21 en growth, gene expression, and cell size in cyanobacteria.

22 function gained following the acquisition of cyanobacteria.

23 trophic Thaumarchaeota, and photoautotrophic Cyanobacteria.

24 -subunit might have a regulatory function in cyanobacteria.

25 aving the fastest measured growth rate among cyanobacteria.

26 lants and bryophytes but absent in algae and cyanobacteria.

27 the light-harvesting phycobilisomes (PBS) in cyanobacteria.

28 esent two novel filament-forming proteins in cyanobacteria.

29 ich appears analogous to what is observed in cyanobacteria.

30 this to the extent required of desert crust cyanobacteria.

31 and copepod grazing on these picoplanktonic cyanobacteria.

32 cyanophycin (C(10)H(19)N(5)O(5)) granules in cyanobacteria.

33 ) governs photoprotection in the majority of cyanobacteria.

34 toxic natural products which are produced by cyanobacteria.

35 trogen fixation rates in pelagic unicellular cyanobacteria.

36 tic transcripts despite being outnumbered by Cyanobacteria.

37 the ALC is widely distributed among diverse cyanobacteria.

38 s cyanobacteria in comparison to unicellular cyanobacteria.

39 rated the highest productivity of sucrose in cyanobacteria.

40 nce of cobalt-dependent metabolism in marine cyanobacteria.

41 lect proliferation of nitrogen-fixing marine cyanobacteria.

42 iated with several bacterial taxa, including cyanobacteria.

43 e bacteria, nevertheless remained unclear in cyanobacteria.

44 thetic reaction centres and the evolution of Cyanobacteria.

45 gest and most ubiquitous groups of bacteria, cyanobacteria.

46 ciated fatty acids (FAs), and an increase in cyanobacteria.

47 2-methylhopanoid production by extant marine cyanobacteria.

48 carbonate coatings that entombed filamentous cyanobacteria.

49 except for a single lineage of endosymbiotic cyanobacteria.

50 Firmicutes (67.8%), Proteobacteria (18.4%), Cyanobacteria (8.9%), and Bacteroidetes (3.1%).

51 Cyanobacteria, a group of photosynthetic prokaryotes, ar

52 In cyanobacteria, a homologous protein (activase-like cyano

53 Interestingly, in cyanobacteria, algae, and plants, FeCh possesses a conse

54 e years, both treatments negatively affected cyanobacteria, although the effects of monsoon delay wer

55 boratory cultures and natural populations of cyanobacteria and algae at single cell resolutions.

56 the toolbox of components and techniques for cyanobacteria and algae is rapidly increasing.

57 ature, supporting the hypothesis that marine cyanobacteria and algae possess distinctive metabolomes.

58 Although cyanobacteria and algae represent a small fraction of th

59 ansitions between an oxic state dominated by cyanobacteria and an anoxic state with sulfate-reducing

60 ke amino acids (MAAs) are widely reported in cyanobacteria and are known to be induced under ultra-vi

61 ys essential roles in carbon assimilation in cyanobacteria and chemoautotrophs.

62 nd nutrient enrichment was detected for both cyanobacteria and chlorophyll-a demonstrating that ecolo

63 me functional groups such as nitrogen-fixing cyanobacteria and denitrifiers may be net beneficiaries

64 Limited presence of Cyanobacteria and detection of algae-associated bacteria

65 Cyanobacteria and diatoms formed distinctly coloured zon

66 Quite unexpectedly, cyanobacteria and Escherichia coli appear to share an in

67 Here we purify holo-CCP2 directly from cyanobacteria and establish that it natively binds canth

68 population growth rate across phytoplankton (Cyanobacteria and eukaryotic microalgae) and prokaryotes

69 ophic communities of photosynthetic algae or cyanobacteria and heterotrophic bacteria or fungi are pe

70 loride-binding characteristics exist between cyanobacteria and higher plants.

71 only significant difference between PSII in cyanobacteria and higher plants.

72 y found in the genomes of phages that infect cyanobacteria and increase the fitness of the cyanophage

73 )) led to the dominance of chlorophytes over cyanobacteria and lower microcystin content.

74 biophotovoltaic cells exploit the ability of cyanobacteria and microalgae to convert light energy int

75 n (PCB), a phycobilin naturally occurring in cyanobacteria and only a few eukaryotic phototrophs, JSC

76 olically engineered yeast, Escherichia coli, cyanobacteria and other microorganisms have been develop

77 taxa) and 18 fossil calibrations across all Cyanobacteria and photosynthetic eukaryotes.

78 nt findings related to diurnal metabolism in cyanobacteria and present open questions in the field.

79 icrobiomes were dominated by Actinobacteria, Cyanobacteria and Proteobacteria but were heavily impact

80 Swapping cyclases between cyanobacteria and purple phototrophic bacteria reveals t

81 n present in the light-harvesting complex of cyanobacteria and red algae.

82 xes found in the photosynthetic apparatus of cyanobacteria and rhodophyta that harvest solar energy a

83 be applied to mapping the proteomes of other cyanobacteria and single-celled organisms.

84 2)-fixing organelles that are present in all cyanobacteria and some chemoautotrophs and that substant

85 totrophy was not an ancestral feature of the Cyanobacteria and that Oxyphotobacteria acquired the gen

86 Synteny among filamentous cyanobacteria and the similar expression patterns for hm

87 t processes important for carbon fixation in cyanobacteria and the survival of enteric bacteria.

88 Long-term coexistence between unicellular cyanobacteria and their lytic viruses (cyanophages) in t

89 ly, we quantify the relative contribution of cyanobacteria and viruses to photosystem-II psbA (reacti

90 in the process of biofilm formation between cyanobacteria and well-studied type IV pili-producing he

91 ification and proliferation of nitrate-using cyanobacteria and, potentially, eukaryotic phytoplankton

92 ve oligotrophic (e.g., phyla Nitrospirae and Cyanobacteria) and copiotrophic (e.g., phylum Proteobact

93 ae, Clostridiales, Christensenellaceae, YS2 (Cyanobacteria), and Victivallaceae are significantly ass

94 Proteobacteria, Cyanobacteria, and Bacteroidetes dominated the mats duri

95 inococcus-Thermus, then Chlorobi/Chloroflexi/Cyanobacteria, and finally Bacteroidetes/Proteobacteria/

96 errocomicrobia but decreased Actinobacteria, Cyanobacteria, and Firmicutes as well as a reduced diver

97 anges during OCP-mediated photoprotection in cyanobacteria, and furnish a basis for understanding the

98 ve [4Fe-4S] cluster protein, whereas plants, cyanobacteria, and some phototrophic bacteria possess an

99 suggest the symbiosis of G. magellanica with cyanobacteria, and trees and shrubs with mycorrhizas, to

100 Cyanobacteria are a key biotic component as primary prod

101 Cyanobacteria are a model photoautotroph and a chassis f

102 e within the carboxysome shell with Rubisco, cyanobacteria are able to overcome the limitations of Ru

103 Cyanobacteria are among only a few organisms that natura

104 Cyanobacteria are an evolutionarily and ecologically imp

105 Cyanobacteria are an integral part of Earth's biogeochem

106 cripts suggested that more living members of Cyanobacteria are associated with the photosynthetic lay

107 Cyanobacteria are attractive microbial hosts for product

108 We show that these printed cyanobacteria are capable of generating a sustained elec

109 Cyanobacteria are common in symbiotic relationships with

110 Cyanobacteria are complex prokaryotes, incorporating a G

111 g, genetically amenable, and stress-tolerant cyanobacteria are desirable as chassis for such applicat

112 Cyanobacteria are important phytoplankton in the Baltic

113 Marine cyanobacteria are infected by phages whose genomes encod

114 rom atmospheric CO2 Growth and metabolism of cyanobacteria are inherently tied to the diurnal rhythm

115 Cyanobacteria are major sources of oxygen, nitrogen, and

116 It is still unclear, however, which Cyanobacteria are most closely related to the chloroplas

117 Cyanobacteria are photosynthetic prokaryotes showing gre

118 Cyanobacteria are photosynthetic prokaryotes that are in

119 Phycocyanins from cyanobacteria are possible sources for new natural blue

120 N(2)-fixing cyanobacteria are symbiotic with diatoms and haptophytes

121 Oceanic cyanobacteria are the most abundant oxygen-generating ph

122 Cyanobacteria are unicellular prokaryotic algae that per

123 Synechococcus cyanobacteria are widespread in the marine environment,

124 Carboxysomes, protein-coated organelles in cyanobacteria, are important in global carbon fixation.

125 lity attributes of the carotenoid profile in cyanobacteria as functional foods.

126 might be conserved in other differentiating cyanobacteria as HetL homologues are spread across the p

127 bionts, most dramatically in the unicellular cyanobacteria associated with haptophytes, which have lo

128 We found that the cyanobacteria attached onto high surface energy crystal

129 so find geosmin-as well as geosmin-producing cyanobacteria-attractive.

130 Several taxa from Cyanobacteria, Bacteroidetes, and Fusobacteria were more

131 s the photogranules grow larger, filamentous cyanobacteria become enriched while other phototrophic m

132 pioneers were succeeded by, amongst others, cyanobacteria belonging to the genera Leptolyngbya, Lyng

133 -2 mm thick red mat dominated by filamentous Cyanobacteria, below which Green Sulfur Bacteria (GSB, C

134 ry of photosystem II (PSII) protein-films to cyanobacteria biofilms to derive: (i) the losses in ligh

135 otemporal mean of weekly or biweekly maximum cyanobacteria biomass for the season or year.

136 abated OW and OA, namely in regulating toxic cyanobacteria blooms on coral reefs.

137 Microcystins, as secondary metabolite of cyanobacteria (blue-green algae) and cyclic heptapeptide

138 hwater lakes, harmful algal blooms (HABs) of Cyanobacteria (blue-green algae) produce toxins that imp

139 (90)Sr and (226)Ra was not intrinsic to all cyanobacteria but was likely a specific biological trait

140 rd the size of the genome of closely related cyanobacteria, but 10-fold larger than most plastid geno

141 ncodes a protein that is highly conserved in cyanobacteria, but of unknown function.

142 O(2) conditions in a manner similar to other cyanobacteria, but Prochlorococcus strains had significa

143 The production of toxins by bloom-forming cyanobacteria can lead to drinking water crises, such as

144 Cyanobacteria can produce a variety of cyanopeptides, ye

145 Cyanobacteria can sense various wavelengths of light and

146 fect primary producers (i.e., plants, algae, cyanobacteria) can have particularly strong effects beca

147 cal role of PntAB in oxygenic photosynthetic cyanobacteria capable of both autotrophic and heterotrop

148 ured organisms related to the photosynthetic Cyanobacteria (class Oxyphotobacteria), including member

149 the class Melainabacteria and a new class of Cyanobacteria (class Sericytochromatia) that is basal to

150 hotosynthesis by integrating components of a cyanobacteria CO2-concentrating mechanism will necessita

151 Cyanobacteria comprise a phylum defined by the capacity

152 rface communities of lichens, mosses, and/or cyanobacteria comprise up to 70% of dryland cover and he

153 hat predicts the effect of climate change on cyanobacteria concentrations in large reservoirs in the

154 y associate geosmin with microbes, including cyanobacteria consumed by larvae [2], who also find geos

155 anotoxins will allow a comprehensive risk of cyanobacteria-containing waters, preventing disease and

156 Microalgae and cyanobacteria contribute roughly half of the global phot

157 ical factors related to treatment effects on cyanobacteria cover and soil surface roughness following

158 and marine heterocyst-forming (N(2)-fixing) cyanobacteria did.

159 Biologically diverse organisms (e.g., cyanobacteria, dinoflagellates, beetles) produce structu

160 ster regulator of circadian transcription in cyanobacteria, driving genome-wide oscillations in mRNA

161 in the adaptive strategies of Synechococcus cyanobacteria during the colonization of novel thermal n

162 In cyanobacteria, ECS signals have never been used for phys

163 The genomes of cyanobacteria encode one of these pathways but never bot

164 teobacteria); is populated by photosynthetic Cyanobacteria exhibiting heterotrophic nutrition (Caloth

165 In low-iron environments, cyanobacteria express IsiA, a PSI antenna, critical to t

166 Plants, algae, and cyanobacteria fix carbon dioxide to organic carbon with

167 lities of most optical sensors detecting the cyanobacteria fluorescent pigments.

168 a significant barrier to the exploitation of cyanobacteria for biotechnological and biomedical applic

169 a spicata and Citrus limon were expressed in cyanobacteria for limonene production.

170 udy presents a feasible strategy to engineer cyanobacteria for photosynthetic production of isoprenoi

171 future biorefineries will deploy engineered cyanobacteria for the conversion of carbon dioxide to us

172 nit of the photosynthetic antenna complex in cyanobacteria, for STORM and SIM imaging.

173 Synechococcus, a genus of unicellular cyanobacteria found throughout the global surface ocean,

174 Here, we investigated resistance in marine cyanobacteria from the genera Synechococcus and Prochlor

175 ceeds by the Calvin-Benson-Bassham cycle, in Cyanobacteria, Gammaproteobacteria, and, surprisingly, G

176 and molecular physiology of Chl f-containing cyanobacteria has been unraveled in culture studies, the

177 Both green algae (charophytes) and cyanobacteria have also been documented locally.

178 Cyanobacteria have attracted much attention as hosts to

179 Cryptogamic species and their associated cyanobacteria have attracted the attention of biogeochem

180 ent an overview of the unique chemistry that cyanobacteria have been co-opted to perform.

181 Although cyanobacteria have been engineered to produce various co

182 o-occurrence analysis of Hps orthologs among cyanobacteria identified an extended set of putative Hps

183 In this investigation, cyanobacteria in a wetland bioreactor enabled the precip

184 a higher proportion of CCRPs in filamentous cyanobacteria in comparison to unicellular cyanobacteria

185 large quantities of cyanotoxins produced by cyanobacteria in eutrophic water.

186 Harmful algal blooms (HABs) caused by cyanobacteria in freshwater environments produce toxins

187 dwide extended and common toxins produced by cyanobacteria in freshwater.

188 Temporal variability of toxins produced by cyanobacteria in lakes is relatively unknown at time sca

189 e gut from the perspective of managing toxic cyanobacteria in lakes, and discuss practical aspects su

190 dible algae in spring to relatively inedible cyanobacteria in summer.

191 w concentrations of cobalt in marine waters, cyanobacteria in the genus Prochlorococcus retain the ge

192 ndant and widespread nitrogen (N(2) )-fixing cyanobacteria in the ocean.

193 fected abundance and composition of biocrust cyanobacteria in two grassland ecosystems.

194 ochrome c (6) in darkness (about 60% in both cyanobacteria, in our experiments), the conductivity of

195 articles (Cl NPs) in selectively eliminating cyanobacteria, including the universal bloom-forming spe

196 These results indicate that cyanobacteria influence the fate and composition of iron

197 ae could convert pseudocobalamin produced by cyanobacteria into cobalamin.

198 dents involving microcystins, are within the cyanobacteria (intracellular) until released into the su

199 Because the livelihood of cyanobacteria is directly dependent upon light, a compre

200 g the origins of oxygenic photosynthesis and Cyanobacteria is key when piecing together the events ar

201 Thus, the competence state in cyanobacteria is regulated by the circadian clock and ca

202 ne obstacle to large-scale implementation of cyanobacteria is their limited growth rates as compared

203 Microcystin-LR-produced by cyanobacteria-is linked with various adverse health effe

204 ast to the well-studied uptake mechanisms in cyanobacteria, it is largely unknown how Mn is distribut

205 d with high levels of mercury, phosphate and cyanobacteria known to produce deadly toxins.

206 Most members of the phylum Cyanobacteria lack Lon (including the model cyanobacteri

207 The origin of oxygenic photosynthesis in Cyanobacteria led to the rise of oxygen on Earth 2.3 bil

208 Effects of biocrust type (cyanobacteria, lichen, moss, mixed), soil texture (sand,

209 Cyanobacteria likely passed these features of transcript

210 en compared to homologs in free-living alpha-cyanobacteria, likely reflecting the homogeneous intrace

211 The photosynthetic capabilities of cyanobacteria make them interesting candidates for indus

212 Carbon fixation in cyanobacteria makes a major contribution to the global c

213 hortest reported doubling time (2.1 h) among cyanobacteria, making it a promising platform for the so

214 PSI-enriched domains in cyanobacteria might foreshadow the partitioning of PSI i

215 These proteins are found in cyanobacteria, mosses, and microalgae, but have been los

216 Among the filamentous, heterocyst-forming cyanobacteria, motility is usually confined to specializ

217 These results imply that cyanobacteria must convert a fraction of the available l

218 In cyanobacteria, nitrogen homeostasis is maintained by an

219 hlights that this genus is distinctive among cyanobacteria, not only in the number of secondary metab

220 oteins (HCPs), have been found among diverse cyanobacteria, occurring as multiple paralogous groups,

221 The marine cyanobacteria of the genus Synechococcus are important p

222 granule dominated by filamentous and motile cyanobacteria of the order Oscillatoriales.

223 Cyanobacteria of the Prochlorococcus and marine Synechoc

224 responsible for triacylglycerol synthesis in cyanobacteria opens the possibility of using prokaryotic

225 Individual cells of cyanobacteria or algae are supplied with light in a high

226 n consumers evolving increasing tolerance to cyanobacteria over time.

227 tudinal distribution of marine Synechococcus cyanobacteria partly relies on the differentiation of li

228 In plants, algae and cyanobacteria, Photosystem II (PSII) catalyzes the light

229 ndently in distantly related lineages of the Cyanobacteria phylum.

230 The waterbody was largely dominated by the cyanobacteria Planktothricoides spp., together with the

231 sition as increases in pH favor more diverse cyanobacteria populations.

232 Cyanobacteria possess a family of one-helix high light-i

233 Cyanobacteria possess two enzymes, acyl-acyl carrier pro

234 While, during summer when cyanobacteria predominated, the significance of Q increa

235 Currently defined ecotypes in marine cyanobacteria Prochlorococcus and Synechococcus likely c

236 Cyanobacteria produce structurally and functionally dive

237 y low light enriched in NIR and inhabited by cyanobacteria producing NIR-absorbing pigments.

238 ein level, starting with a primitive form in cyanobacteria, RCA of chlorophytes evolved by integratin

239 Phycobilins are light-harvesting pigments of cyanobacteria, red algae, and cryptophytes.

240 Phototrophic unicellular cyanobacteria related to Synechococcus and Prochlorococc

241 oreover, Synechocystis, a nonbiomineralizing cyanobacteria, removed only 14 and 25% of (226)Ra and (9

242 g diatoms, cryptophytes and greens to summer cyanobacteria) resulted in consumers evolving increasing

243 A study on thermophilic cyanobacteria reveals how environmentally induced phenot

244 In cyanobacteria, Rubisco enzymes are densely packed and en

245 cterize a CRISPR-associated transposase from cyanobacteria Scytonema hofmanni (ShCAST) that consists

246 ersimplification of global change effects on cyanobacteria should be avoided; stressor gradients and

247 This process is complicated in cyanobacteria, since many, including Synechocystis sp. P

248 bundances of five phyla, namely Tenericutes, Cyanobacteria, Spirochaetes, Elusimicrobia and Lentispha

249 erse, with prevalence of UCYN-A (unicellular cyanobacteria, subcluster 1B) and non-cyanobacterial dia

250 cool-adapted by warm-adapted nitrogen-fixing cyanobacteria (such as Scytonema) and a switch in the do

251 teriaceae (Bacteriodetes), and the phylum of cyanobacteria (such as the Phormidium genus) can be iden

252 Close phylogenetic neighbors to Cyanobacteria, such as Margulisbacteria (RBX-1 and ZB3),

253 than the best-known free-living N(2)-fixing cyanobacteria, suggesting they may be equally or more im

254 of sigma factor in metabolic engineering of cyanobacteria, summarizes the challenges in the path tow

255 ce, ultimately killing the cell, while other cyanobacteria survive due to resistance to infection.

256 The cyanobacteria survived the encounter despite late-stage

257 ding to carotenoid band shifts, in the model cyanobacteria Synechococcus elongatus PCC7942 and Synech

258 ed with a competing and potentially invasive cyanobacteria (Synechocystis sp. PCC6803).

259 Even in the presence of cobalamin, Cyanobacteria synthesize pseudocobalamin-likely reflecti

260 is controlled and structured differently in cyanobacteria than in heterotrophic bacteria.

261 nin has demonstrated to be more selective to cyanobacteria than other pigments, such as chlorophyll-a

262 Cyanobacteriochromes are photoreceptors in cyanobacteria that exhibit a wide spectral coverage and

263 the chlorophyll-containing plants, algae and cyanobacteria that make up the oxygenic phototrophs and

264 We propose that, in cyanobacteria, the CTDHs are carotenoid donors to HCPs.

265 Unlike rubiscos from plants and cyanobacteria, the fastest variants discovered here are

266 In cyanobacteria, the photoprotective role is played by a s

267 onditions and inhibit the recruitment of the cyanobacteria, thereby preventing the reoccurrence of cy

268 Synechococcus, a globally important group of cyanobacteria, thrives in various light niches in part d

269 In cyanobacteria, timing is generated by a posttranslationa

270 t recently discovered chlorophylls, enabling cyanobacteria to harvest near-infrared radiation (NIR) a

271 isms, one of the most crucial parameters for cyanobacteria to monitor is light.

272 cific (OPS) subunits that are conserved from cyanobacteria to plants(3,6).

273 These differential sensitivities of cyanobacteria to rising temperatures and decreasing prec

274 Irrigation with eutrophic water containing cyanobacteria toxins poses a potential risk to soil anim

275 he prominent marine dinitrogen (N(2))-fixing cyanobacteria Trichodesmium to ocean acidification (OA)

276 Palyhtoa), dinoflagellates (Ostreopsis), and cyanobacteria (Trichodesmium).

277 s oxygen-sensitive nitrogenase [11, 12], and cyanobacteria typically exhibit temperature-induced plas

278 Cyanobacteria unable to fix atmospheric nitrogen have ev

279 increased the relative abundance of N-fixing cyanobacteria (up to 0.34 as fraction of total reads), c

280 Cyanobacteria use one of two pathways to synthesize alka

281 Yet, the mechanism that euendolithic cyanobacteria use to excavate solid carbonates suggests

282 underlie the regulation of photosynthesis in cyanobacteria using ensemble-based measurements remains

283 Cyanobacteria utilize a CO(2)-concentrating mechanism (C

284 Phototrophic organisms such as cyanobacteria utilize the sun's energy to convert atmosp

285 Cyanobacteria was dominant in both areas, but the relati

286 ignificantly decreased and Bacteroidetes and Cyanobacteria was increased compared to baseline and was

287 in both areas, but the relative abundance of Cyanobacteria was much higher in the emerged areas than

288 icantly increased, whereas Bacteroidetes and Cyanobacteria were decreased.

289 ion (qPCR), we discovered that toxin-forming cyanobacteria were present before visible blooms and tox

290 In contrast, cyanobacteria were stimulated with increasing Fe concent

291 phic organisms, including plants, algae, and cyanobacteria, where it is referred to as photorespirati

292 e found broadly throughout eukaryotes and in cyanobacteria, where they generate circadian (about a da

293 far-red light photoacclimation in a range of cyanobacteria, which enables them to use near-infrared-r

294 ning (MoClo) system is not yet available for cyanobacteria, which lag behind other prokaryotes in syn

295 is balanced by nitrogen fixation mediated by cyanobacteria, which may form extensive blooms in surfac

296 tive cyanocidal compounds that can eliminate cyanobacteria while preserving algal members of the phyt

297 ersatile system called CyanoGate that unites cyanobacteria with plant and algal systems.

298 n of just a few heterologous genes can endow cyanobacteria with the ability to transform specific cen

299 otosynthesis by endolithic, Chl f-containing cyanobacteria within natural beachrock biofilms that are

300 In cyanobacteria without specialized N(2)-fixing cells (het