ライフサイエンスコーパス: Prochlorococcus

1 ter in the oceans, the marine cyanobacterium Prochlorococcus.

2 ncouraged us to explore similar methods with Prochlorococcus.

3 nophages may be the origin of these genes to Prochlorococcus.

4 and field data for the marine cyanobacterium Prochlorococcus.

5 contributions similar to the cyanobacterium Prochlorococcus.

6 ted picoeukaryotes and Synechococcus but not Prochlorococcus.

7 appear to play a role in light harvesting in Prochlorococcus.

8 types analogous to the marine cyanobacterium Prochlorococcus.

9 ridae) that infect the marine cyanobacterium Prochlorococcus.

10 ons in samples that are usually dominated by Prochlorococcus.

11 s and predators of abundant bacteria such as Prochlorococcus.

12 ubstantially limit the geographical range of Prochlorococcus.

13 reamlining along a major early branch within Prochlorococcus.

14 er abundant microbes such as SAR11, OM43 and Prochlorococcus.

15 sicles produced by the marine cyanobacterium Prochlorococcus.

16 n by cyanobacteria, namely Synechococcus and Prochlorococcus.

17 the globally abundant marine cyanobacterium Prochlorococcus.

18 ion gene content of the marine cyanobacteria Prochlorococcus [1-4] and its viruses (cyanophages).

19 ore Synechococcus (4.8%-12.1%) infected than Prochlorococcus (2.5%-6.2%), whereas T7-like cyanophages

20 -fixing picocyanobacteria (Synechococcus and Prochlorococcus [6]).

21 of variability in cell volume was 5-fold for Prochlorococcus, 8-fold for Synechococcus and 6-fold for

22 tribution, and availability of isolates make Prochlorococcus a model system for understanding marine

23 Here, we report that cultures of Prochlorococcus, a numerically dominant marine cyanobact

24 7 x 10(3) to 1.2 x 10(5) cells.mL(-1), while Prochlorococcus abundances were relatively low overall,

25 g the taxonomy of putative host genera, with Prochlorococcus, Acanthochlois and members of the SAR86

26 ight ecotypes of the abundant cyanobacterium Prochlorococcus across a meridional transect in the cent

27 rs to diagnose ocean metabolism demonstrated Prochlorococcus actively and simultaneously deploying mu

28 Prochlorococcus adapt to local environments by gene gain

29 Model parameters are presented for Prochlorococcus adding to those previously presented for

30 Ocean, we found that natural populations of Prochlorococcus adhered to Redfield ratio dimensions whe

31 oflagellates as the most active predators of Prochlorococcus, alongside a radiolarian, chrysophytes,

32 Now, it is shown that cyanophages infecting Prochlorococcus also contain genes for phycobilin-synthe

33 al gene transfer (HGT) in bacteria, but, for Prochlorococcus, an abundant marine cyanobacterium, how

34 ise substantial biosynthetic demand for N in Prochlorococcus and a range of other microbial taxa.

35 ely host-specific, whereas low-light-adapted Prochlorococcus and all strains of Synechococcus yielded

36 hli genes are expressed during infection of Prochlorococcus and are co-transcribed with essential ph

37 nobacteria from the genera Synechococcus and Prochlorococcus and compared modes of resistance against

38 provides unique insight into the ecology of Prochlorococcus and could potentially be expanded to inc

39 ere identified along the cruise transect for Prochlorococcus and eight for Synechococcus Although Pro

40 atory co-cultures between the cyanobacterium Prochlorococcus and eight heterotrophic bacteria.

41 Spontaneous resistance occurs frequently in Prochlorococcus and is often accompanied by a pleiotropi

42 omplexity of the interaction network between Prochlorococcus and its phages in nature.

43 ations for understanding the biogeography of Prochlorococcus and its role in the oceanic carbon and n

44 of the unicellular planktonic cyanobacteria Prochlorococcus and marine Synechococcus belong to a sin

45 Cyanobacteria of the Prochlorococcus and marine Synechococcus genera are the

46 PSHCP is not only found in all sequenced Prochlorococcus and marine Synechococcus genomes, but it

47 ans, resulting in the diversification of the Prochlorococcus and marine Synechococcus lineages from a

48 n all cyanobacterial genomes except those of Prochlorococcus and marine Synechococcus species.

49 equence analyses focusing on five strains of Prochlorococcus and one strain of marine A Synechococcus

50 The rapid transcriptional responses of both Prochlorococcus and Pelagibacter populations suggested t

51 ates that infect the dominant bacterial taxa Prochlorococcus and Pelagibacter, usually regarded as co

52 gene content for two model marine microbes, Prochlorococcus and Pelagibacter, within and between pop

53 ant members of the marine microbiome such as Prochlorococcus and Pelagibacter.

54 and the phytoplankton groups Synechococcus, Prochlorococcus and picoeukaryotic phytoplankton) in the

55 considered to understand the biogeography of Prochlorococcus and predict its changes under future oce

56 Moreover, the metabolic codependencies of Prochlorococcus and SAR11 are highly similar to those of

57 phate-chased cells, we demonstrate that both Prochlorococcus and SAR11 cells exploit an extracellular

58 l surface oligotrophic clades (SAR116, OM75, Prochlorococcus and SAR11 Ia) were relatively depleted i

59 and that most belong to the abundant groups Prochlorococcus and SAR11.

60 Viruses that infect Prochlorococcus and Synechococcus (cyanophages) can be r

61 hotosynthetic cells, the picocyanobacteria - Prochlorococcus and Synechococcus - play a fundamental g

62 The Cyanobacteria Prochlorococcus and Synechococcus account for a substant

63 2)/b(2) and phycobilisome antennas in extant Prochlorococcus and Synechococcus appear to play a role

64 The annual mean global abundances of Prochlorococcus and Synechococcus are 2.9 +/- 0.1 x 10(2

65 Prochlorococcus and Synechococcus are abundant unicellul

66 The marine cyanobacteria Prochlorococcus and Synechococcus are highly abundant in

67 The cyanobacteria Prochlorococcus and Synechococcus are important marine p

68 The photosynthetic picocyanobacteria Prochlorococcus and Synechococcus are models for dissect

69 Marine picocyanobacteria of the genera Prochlorococcus and Synechococcus are the most numerous

70 Prochlorococcus and Synechococcus are the two most abund

71 nutrient addition resulted in an increase in Prochlorococcus and Synechococcus cell size.

72 anophages infecting the marine cyanobacteria Prochlorococcus and Synechococcus encode and express gen

73 iptomes of the abundant marine cyanobacteria Prochlorococcus and Synechococcus identified responses t

74 tly defined ecotypes in marine cyanobacteria Prochlorococcus and Synechococcus likely contain subpopu

75 c prediction of the exported pan-proteome of Prochlorococcus and Synechococcus lineages demonstrated

76 Finally, both Prochlorococcus and Synechococcus strain-specific cyanop

77 s of the ubiquitous marine picocyanobacteria Prochlorococcus and Synechococcus Unlike other lanthipep

78 the two most abundant marine cyanobacteria, Prochlorococcus and Synechococcus, produce and accumulat

79 increases in cell numbers of 29% and 14% for Prochlorococcus and Synechococcus, respectively.

80 interaction between the marine cyanobacteria Prochlorococcus and Synechococcus, the intercellular mem

81 Marine picocyanobacteria Prochlorococcus and Synechococcus, the most abundant pho

82 origin have been found in phages that infect Prochlorococcus and Synechococcus, the numerically domin

83 Previous studies suggested that Prochlorococcus and Synechococcus, the numerically domin

84 Marine picocyanobacteria of the genera Prochlorococcus and Synechococcus, the two most abundant

85 s and contributions to primary production of Prochlorococcus and Synechococcus, these changes may hav

86 plankton including the prokaryotic lineages, Prochlorococcus and Synechococcus.

87 Additional reconstructions suggest that Prochlorococcus and the dominant cooccurring heterotroph

88 ine of the oligotrophic and photoautotrophic Prochlorococcus and the enrichment of heterotrophic taxa

89 ve network of photosynthetic lamellae within Prochlorococcus and the potential pathways for intracell

90 ysis of historical BATS data showed enhanced Prochlorococcus and virus-like particle abundances assoc

91 ecause of reduced nutrient supply (excepting Prochlorococcus) and were generally more sensitive to ma

92 ns of nutrients and organic carbon, abundant Prochlorococcus, and high microbial community alpha dive

93 ort the isolation of cyanophages that infect Prochlorococcus, and show that although some are host-st

94 ortant factor underlying the distribution of Prochlorococcus, and thought to explain, in part, low ab

95 evated cyanophage abundance and infection of Prochlorococcus, and transcriptomic evidence of increase

96 re, we present a scenario to explain how the Prochlorococcus antenna might have evolved in an ancestr

97 r cyanobacteria related to Synechococcus and Prochlorococcus are associated with a number of groups.

98 erse clades of the unicellular cyanobacteria Prochlorococcus are biogeographically structured along e

99 Our results suggest that Prochlorococcus are primary producers capable of tuning

100 Marine picocyanobacteria of the genus Prochlorococcus are the most abundant photosynthetic org

101 involving the in situ community, and labeled Prochlorococcus as prey, revealed choanoflagellates as t

102 Here single-cell measurements reveal that Prochlorococcus at the base of the photic zone in the Ea

103 These include Prochlorococcus at the coast and Cyanobium-related seque

104 alysing distinct co-occurring populations of Prochlorococcus at two locations in the North Atlantic.

105 In surface waters, Prochlorococcus averaged 11.7 +/- 4.4 x 10(4) cells ml(-

106 The ubiquitous SAR11 and Prochlorococcus bacteria manage to maintain a sufficient

107 ic, growth-securing adaptation for SAR11 and Prochlorococcus bacteria, which lack internal reserves t

108 s are among the lowest measured globally but Prochlorococcus biomass is high.

109 We have shown in laboratory experiments that Prochlorococcus can take up glucose.

110 challenges 2 long-held assumptions that (i) Prochlorococcus cannot assimilate nitrate, and (ii) only

111 o different winter-time cruises to show that Prochlorococcus cell production and mortality rates are

112 ctly by the day/night cycle or indirectly by Prochlorococcus cell production.

113 dynamics in which most of the newly produced Prochlorococcus cells are consumed each night likely enf

114 and nitrate assimilation genes in uncultured Prochlorococcus cells from marine surface waters.

115 apparent paradox of a multitude of resistant Prochlorococcus cells in nature that are growing close t

116 Sargasso Sea supports this hypothesis; most Prochlorococcus cells in this low-P environment contain

117 rmal stratification, on average 8-10% of the Prochlorococcus cells live without enough light to susta

118 these islands are variable among cooccurring Prochlorococcus cells.

119 is gap, here we use the numerically dominant Prochlorococcus clade eHL-II (eMIT9312) as a model organ

120 sinks in the photosynthetic pathway in other Prochlorococcus clades from high-light environments.

121 Their distribution among several Prochlorococcus clades further suggests that the genes e

122 revealed the presence of two uncharacterized Prochlorococcus clades.

123 Quantitative descriptions of Prochlorococcus cobalt limitation are used to interpret

124 Inhibition was consistently greater for Prochlorococcus compared to two strains of Synechococcus

125 hic interaction with the per-capita rates of Prochlorococcus consumption driven either directly by th

126 yanobacteria, including members of the genus Prochlorococcus, contain icosahedral protein microcompar

127 A amplification procedure was validated with Prochlorococcus cultures and then applied to a microbial

128 that smaller particles generated from lysed Prochlorococcus cultures are organically enriched and nu

129 number densities to particles generated from Prochlorococcus cultures.

130 lts highlight the potential vulnerability of Prochlorococcus-dependent marine ecosystems to future wa

131 Prochlorococcus describes a diverse and abundant genus o

132 Our findings thus suggest that Prochlorococcus diverged from other cyanobacteria under

133 Prochlorococcus division rates appear primarily determin

134 criptional activity coincided with a peak in Prochlorococcus DNA replication, indicating coordinated

135 cific Oxygen Deficient Zone (ETNP ODZ) where Prochlorococcus dominates a secondary chlorophyll maximu

136 -light conditions occupied by their hosts, a Prochlorococcus ecotype endemic to ODZs.

137 Prochlorococcus ecotypes are a useful system for explori

138 Gene expression data for Prochlorococcus ecotypes MED4 and MIT9313 allow users to

139 their small size and their economized genome Prochlorococcus ecotypes typically possess a single futA

140 ages within high- and low-light (LL) adapted Prochlorococcus ecotypes.

141 The marine picocyanobacterium Prochlorococcus exhibits high genomic plasticity, yet th

142 Although green cyanobacteria of the genus Prochlorococcus express genes encoding enzymes that dire

143 The cyanobacterium Prochlorococcus exudes both compound classes, which meta

144 vated anoxic marine zone (AMZ) IB lineage of Prochlorococcus from pelagic oxygen-deficient zones (ODZ

145 This switching ability of the Prochlorococcus FutA protein may reflect ecological adap

146 Sequencing of a Prochlorococcus genome purified from yeast identified 14

147 he ability to use nitrate across hundreds of Prochlorococcus genomes to better understand the modes o

148 Genes present in the variable regions of Prochlorococcus genomes were among the most highly expre

149 ted evening onset of cell division and rapid Prochlorococcus growth between 1.5 and 3.1 div day(-1),

150 ropical Atlantic rates, our results indicate Prochlorococcus growth rates should be reevaluated with

151 ajority of cyanobacteria use phycobilisomes, Prochlorococcus has evolved to use a chlorophyll a(2)/b(

152 Prochlorococcus has remained a genetically intractable b

153 on datasets, we observed higher abundance of Prochlorococcus high-light I (HLI) and low-light I (LLI)

154 ococcus and eight for Synechococcus Although Prochlorococcus HLIIIA and HLIVA ESTUs codominated in ir

155 Synechococcus and Prochlorococcus HNLC ecotypes likewise exhibit independe

156 ate photosynthesis during infection of their Prochlorococcus hosts in the tropical oceans.

157 High-light-adapted Prochlorococcus hosts yielded Podoviridae exclusively, w

158 of the ecologically important cyanobacterium Prochlorococcus in a near-native state using cryo-electr

159 hought to explain, in part, low abundance of Prochlorococcus in coastal, temperate, and upwelling zon

160 bes in each environment (Ostreococcus in CC, Prochlorococcus in NPSG) were central determinants of ov

161 We suggest Prochlorococcus in P-limited systems are physiologically

162 e, we were able to observe glucose uptake by Prochlorococcus in the central Atlantic Ocean, where glu

163 As light levels decrease in the fall, Prochlorococcus in the deep euphotic zone experience red

164 l models correctly predicts the dominance of Prochlorococcus in the gyres, and the relative dominance

165 nable discernment of the present P status of Prochlorococcus in the oligotrophic oceans.

166 for previously unrecognized productivity by Prochlorococcus in the presence of oxidized nitrogen spe

167 ral populations of the marine cyanobacterium Prochlorococcus indicate this numerically dominant photo

168 2, and HLIP proteins cluster with those from Prochlorococcus, indicating that they are of cyanobacter

169 Prochlorococcus is a key member of open-ocean primary pr

170 The marine cyanobacterium Prochlorococcus is a main contributor to global photosyn

171 Prochlorococcus is a simple cyanobacterium that is abund

172 t, in an SAR11 subgroup that dominates where Prochlorococcus is abundant, adenine additions to cultur

173 Prochlorococcus is an abundant marine cyanobacterium tha

174 f the dominant photosynthetic cyanobacterium Prochlorococcus is assumed to reflect a simple food web

175 Prochlorococcus is both the smallest and numerically mos

176 The cyanobacterium Prochlorococcus is Earth's most abundant photosynthetic

177 Prochlorococcus is responsible for a significant part of

178 The cyanobacterium Prochlorococcus is the dominant oxygenic phototroph in t

179 The marine cyanobacterium Prochlorococcus is the most abundant photosynthetic orga

180 The cyanobacterium Prochlorococcus is the most effective competitor for acq

181 The cyanobacterium Prochlorococcus is the numerically dominant phototroph i

182 Prochlorococcus is the numerically dominant phototroph i

183 Prochlorococcus is the numerically dominant phytoplankte

184 The marine unicellular cyanobacterium Prochlorococcus is the smallest-known oxygen-evolving au

185 We explore cobalt metabolism in a Prochlorococcus isolate from the equatorial Pacific Ocea

186 Prochlorococcus isolated from surface waters of stratifi

187 istinct from each other and other high-light Prochlorococcus isolates and likely define a previously

188 as between high-light- and low-light-adapted Prochlorococcus isolates, suggesting a mechanism for hor

189 In axenic cultures of Prochlorococcus, it was observed that <1% of the total P

190 tennae is considered a defining attribute of Prochlorococcus Its ecology and evolution are understood

191 the largest evolutionary distance within the Prochlorococcus lineage and that have different minimum,

192 In addition to supporting observations that Prochlorococcus LLI thrive at higher irradiances than ot

193 compare C, N and P content of Synechococcus, Prochlorococcus, low nucleic acid (LNA) content bacterio

194 By mapping this process onto a model of Prochlorococcus' macroevolution, we propose that niche-c

195 kers reported that their Ec-expressed Np and Prochlorococcus marinus (Pm) AD preparations transform a

196 iforme, Synechococcus sp. strain WH8102, and Prochlorococcus marinus MED4, suggesting that the cyanob

197 carboxysomes from the marine cyanobacterium Prochlorococcus marinus MED4.

198 lysis with two other cyanobacterial genomes, Prochlorococcus marinus sp. MED4 and P.marinus sp. MIT93

199 404 confers capability for glucose uptake in Prochlorococcus marinus SS120.

200 (pssm2-Fd), which infects the cyanobacterium Prochlorococcus marinus, revealed high levels of similar

201 ) and (NB)(2) from the marine cyanobacterium Prochlorococcus marinus.

202 ydomonas reinhardtii, and the cyanobacterium Prochlorococcus marinus.

203 ng the ubiquitous open ocean cyanobacterium, Prochlorococcus marinus.

204 Gephyrocapsa huxleyi and the cyanobacterium Prochlorococcus 'marinus' are among Earth's most abundan

205 the 0.1- to 1-microm range (e.g., bacteria, Prochlorococcus) may be more quickly digestible because

206 Studies of the cyanobacterium Prochlorococcus MED4 and its associated cyanophage P-SSP

207 a host and phage, the marine cyanobacterium Prochlorococcus MED4 and the T7-like cyanophage P-SSP7,

208 Two independent crystal structures of Prochlorococcus MED4 CsoS1D reveal three features not se

209 oxic effects of several partial and 15 whole Prochlorococcus MED4 genome clones in S. cerevisiae.

210 uptake kinetic experiments were performed on Prochlorococcus MED4 grown in P-limited chemostats and b

211 Prochlorococcus MED4 has an AT-rich genome, with a GC co

212 Prochlorococcus MED4 has, with a total of only 1,716 ann

213 of evolution, there was a steady increase in Prochlorococcus' metabolic rate and excretion of organic

214 d theoretical calculations all indicate that Prochlorococcus MIT9215 can sustain growth with less tha

215 Whole-genome shotgun sequencing of Prochlorococcus MIT9312 plones showed 62% coverage of th

216 Remarkably, in Prochlorococcus MIT9313 a single promiscuous enzyme tran

217 In Prochlorococcus MIT9313, a single enzyme, ProcM, catalyz

218 This biochemical adaptation by Prochlorococcus must be a significant benefit to these o

219 n by infecting the marine picocyanobacterium Prochlorococcus NATL2A with cyanomyovirus P-SSM2 under P

220 Cruise data also showed Prochlorococcus nitrogen metabolism transcripts consiste

221 sis genes, none of the marine Synechococcus, Prochlorococcus (non-N(2)-fixing), and marine heterocyst

222 s with DOM derived from an axenic culture of Prochlorococcus, or high-molecular weight DOM concentrat

223 or certain strains of both Synechococcus and Prochlorococcus Our findings unveil a heavy cost of prom

224 Under these conditions, Prochlorococcus' poor response to elevated CO(2) disappe

225 e importance of top-down controls in shaping Prochlorococcus population dynamics.

226 of the structure and dynamics of the global Prochlorococcus population.

227 d physiology of these clades may explain why Prochlorococcus populations from iron-depleted regions d

228 The poleward collapse of Prochlorococcus populations then naturally emerges when

229 etic diversity and infection permutations in Prochlorococcus populations, further augmenting the comp

230 echanisms underlying the balanced control of Prochlorococcus populations.

231 itions within the SAR11 clade, enrichment of Prochlorococcus, predicted smaller genome sizes and shif

232 The oceanic picoplankton Prochlorococcus - probably the most abundant photosynthe

233 Accumulation of Prochlorococcus produced by ultradian growth was restric

234 ingle component organic molecules that mimic Prochlorococcus proteins, lipids, and saccharides.

235 hesizing enzymes, and these are expressed in Prochlorococcus, raising further questions as to the rol

236 Prochlorococcus ranged up to 3.14 x 10(5) cells mL(-1) i

237 response to elevated CO(2) disappeared, and Prochlorococcus' relative fitness showed negative freque

238 ultured picocyanobacteria, Synechococcus and Prochlorococcus, release FDOM that closely match the typ

239 Marine cyanobacteria of the genus Prochlorococcus represent numerically dominant photoauto

240 % of the standing stock of Synechococcus and Prochlorococcus, respectively.

241 tric cyanobacterial genera Synechococcus and Prochlorococcus, respectively.

242 in marine waters, cyanobacteria in the genus Prochlorococcus retain the genetic machinery for the syn

243 enrichment of dominant seawater taxa such as Prochlorococcus, SAR11 or Synechococcus was observed sug

244 Similarly, Prochlorococcus showed significantly higher levels of tr

245 secondary metabolites produced by strains of Prochlorococcus, single-cell, planktonic marine cyanobac

246 capsid, a long contractile tail and infects Prochlorococcus sp.

247 w that the moderate low-light-adapted strain Prochlorococcus sp. MIT 9313 has one iron-stress-induced

248 set, in part because Pelagibacter ubique and Prochlorococcus species, which almost entirely lacked th

249 Marine Synechococcus spp and marine Prochlorococcus spp are numerically dominant photoautotr

250 AMZs, was dominated by the picocyanobacteria Prochlorococcus spp.

251 Prochlorococcus spp. CCM components in the Global Ocean

252 As an oligotrophic specialist, Prochlorococcus spp. has streamlined its genome and meta

253 The genomes of Prochlorococcus spp. indicate that they have a simple CC

254 Here, we show that the CCM of Prochlorococcus spp. is effective and efficient, transpo

255 iology or gene expression were observed when Prochlorococcus spp. was fully acclimated to high-CO2 (1

256 r geographic range of this group relative to Prochlorococcus spp., which lack a PBS.

257 echococcus strain was unable to outcompete a Prochlorococcus strain in co-culture at elevated CO(2) .

258 We compared the molecular response of Prochlorococcus strain MED4 to P starvation in batch cul

259 me shell component, CsoS1D, in the genome of Prochlorococcus strain MED4; orthologs were subsequently

260 Because Prochlorococcus strain MIT9301 encodes genes similar to

261 organization of the phoB gene cluster in 11 Prochlorococcus strains belonging to diverse ecotypes an

262 a manner similar to other cyanobacteria, but Prochlorococcus strains had significantly lower realized

263 Here we compare the genomes of two Prochlorococcus strains that span the largest evolutiona

264 he site currently contains the genomes of 13 Prochlorococcus strains, 11 Synechococcus strains and 28

265 ssed the fate of a number of phage-resistant Prochlorococcus strains, focusing on those with a high f

266 ococcus and a subset of high light I-adapted Prochlorococcus strains, suggesting niche specificity.

267 A-->B-->K-->E-->D gene organization and most Prochlorococcus strains.

268 Prochlorococcus stress genes, bottle experiments, and Ea

269 ents are found in microbes co-occurring with Prochlorococcus, suggesting a common mechanism for micro

270 Models do not reproduce total inhibition of Prochlorococcus, suggesting that additional mechanisms s

271 Picophytoplankton populations [Prochlorococcus, Synechococcus (SYN), and picoeukaryotes

272 izing, comparing and curating the genomes of Prochlorococcus, Synechococcus and Cyanobium, the most a

273 sequences from the Global Ocean Survey from Prochlorococcus, Synechococcus and phage genomes are arc

274 espond to the widespread phototrophic clades Prochlorococcus, Synechococcus, and Crocosphaera, whose

275 n to this is a 62-amino-acid protein, termed Prochlorococcus/ Synechococcus hyper-conserved protein (

276 cluding populations of the picocyanobacteria Prochlorococcus that can form a secondary chlorophyll ma

277 hologs of two model organisms from the genus Prochlorococcus that have significantly different GC-con

278 e best examples are the cyanobacterial genus Prochlorococcus, the alphaproteobacterial clade SAR11 an

279 Paradoxically, Prochlorococcus, the cyanobacterium that dominates NPSG

280 Prochlorococcus, the most abundant genus of photosynthet

281 Extensive microdiversity within Prochlorococcus, the most abundant marine cyanobacterium

282 Cultures of Prochlorococcus, the most abundant phytoplankton species

283 For Prochlorococcus, the most abundant phytoplankton, an est

284 structural insights into the carboxysome of Prochlorococcus, the numerically dominant cyanobacterium

285 Prochlorococcus, the numerically dominant primary produc

286 Move over plants-make way for tiny Prochlorococcus, the smallest and most abundant photosyn

287 As in other bacteria, in Prochlorococcus these genes are regulated by the PhoR/Ph

288 Thus, it seems that the adaptation of Prochlorococcus to low light environments has triggered

289 the globally abundant oceanic phytoplankter Prochlorococcus To understand what drove observed evolut

290 this clade, two deeply branching lineages of Prochlorococcus, two lineages of marine A Synechococcus

291 To better understand uptake capabilities of Prochlorococcus under different P stress conditions, upt

292 ls, which use the UGA codon for tryptophane, Prochlorococcus uses the standard genetic code.

293 Prochlorococcus vesicles can support the growth of heter

294 In particular, when applied to Prochlorococcus, we find that glycogen and lipid managem

295 In identifying direct consumers of Prochlorococcus, we reveal food-web linkages of individu

296 pattern in Synechococcus's nearest relative, Prochlorococcus - wherein decreasing genome size has coi

297 gle-celled, planktonic marine cyanobacterium Prochlorococcus-which conducts a sizable fraction of pho

298 erns within the group, and failed to cluster Prochlorococcus with chloroplasts or other chlorophyll b

299 ic relationship analogous to that connecting Prochlorococcus with the 'helper' heterotrophic microbes

300 and the marine photosynthetic cyanobacterium Prochlorococcus, with a diameter of ~600 nm.