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1  in Chlamydomonas reinhardtii, a model algal phototroph.
2 hich may indicate a common function in these phototrophs.
3 -degrading heterotrophs and possibly various phototrophs.
4 e than water for O(2) production by oxygenic phototrophs.
5 r bacteria or heliobacteria are the earliest phototrophs.
6 6.5) to flavocytochromes isolated from other phototrophs.
7 etic carbon yield in cyanobacteria and other phototrophs.
8 ation by the Calvin-Benson cycle in oxygenic phototrophs.
9 ctinobacteria, with abundant algae and other phototrophs.
10 largest photosynthetic complex in anoxygenic phototrophs.
11 taining bacteria that make up the anoxygenic phototrophs.
12 nary link between prokaryotic and eukaryotic phototrophs.
13 paration and water oxidation in all oxygenic phototrophs.
14  in the photorespiratory pathway of oxygenic phototrophs.
15  photosystem II (PSII) in all known oxygenic phototrophs.
16 specialized adaptations in a small number of phototrophs.
17  which is found in all other known groups of phototrophs.
18 ic species belonging to this unique group of phototrophs.
19 sses a melange of traits distinct from known phototrophs.
20 nd), and those typical of modern prokaryotic phototrophs (-25 +/- 10 per thousand).
21                    Purple aerobic anoxygenic phototrophs (AAPs) are the only organisms known to captu
22                                          The phototroph adapted to seawater oligotrophy by reducing i
23 GBT connects the metabolisms of the dominant phototroph and heterotroph in the oceans.
24                                       Marine phototroph and heterotroph interactions are vital in mai
25 ods and services exchange between fungus and phototroph and how this propelled the success of both sy
26 reases, the coexistence between the acquired phototroph and its prey transitions from a stable equili
27  and cyanobacteria that make up the oxygenic phototrophs and a diversity of bacteriochlorophyll-conta
28                   Here we show how microbial phototrophs and autotrophs contribute to this exceptiona
29                 Autotrophic cells, including phototrophs and chemolithotrophs, also use proton gradie
30 xin and its orthologs are unique to oxygenic phototrophs and distinct from rubredoxins in Archaea and
31 rients in the surface ocean between oxygenic phototrophs and Fe(II)-oxidizing, anoxygenic photosynthe
32  we challenge the general belief that marine phototrophs and heterotrophs compete for the same scarce
33           Microbial communities comprised of phototrophs and heterotrophs hold great promise for sust
34         Nutrient exchange mutualisms between phototrophs and heterotrophs, such as plants and mycorrh
35 herol is synthesized exclusively in oxygenic phototrophs and is known to function as a lipid-soluble
36 the particles was positively correlated with phototrophs and MGII in the surface water was negatively
37 erstanding of N(2)O production in eukaryotic phototrophs and represent an important step toward a com
38 a consisting of sulfide-oxidizing anoxygenic phototrophs and sulfate-reducing bacteria.
39 ides an in-depth view of TM architectures in phototrophs and the determinants that shape their forms,
40 potentials that are accessible to anoxygenic phototrophs and thus the most likely building blocks for
41  reversal of water oxidation in contemporary phototrophs and would have been unlikely to influence th
42 iosis) between a photosynthesizing organism (phototroph) and a fungus.
43 l solar exposure, light filtered by oxygenic phototrophs, and light filtered under seawater, we deriv
44 otists, functionally divided into consumers, phototrophs, and parasites act as integral components an
45  that Ycf54 is a cyclase subunit in oxygenic phototrophs, and that different classes of the enzyme ex
46                           However, rhodopsin phototrophs are actually the most abundant metabolic gro
47 pper on heme and chlorophyll biosynthesis in phototrophs are addressed.
48              The (14)C results indicate that phototrophs are also fixing respired CO(2) from heterotr
49 nd evolutionary effects of viruses on marine phototrophs are well recognized, little is known about t
50 rowth (eolian deposited pollen and microbial phototrophs) are abundant and that soils are saturated w
51 urvive in the sediment whereas others (e.g., phototrophs) are simply deposited by sedimentary process
52 n sulfur bacteria and filamentous anoxygenic phototrophs as well as in the genomes of several nonphot
53 rotein complex universally found in oxygenic phototrophs, as a reliable reporter protein to probe mic
54  one uniform, widespread class of anoxygenic phototrophs, as previously proposed; rather, these assem
55 abolic window for the survival of anoxygenic phototrophs, as well as an as-yet unappreciated contribu
56 orococcus indicate this numerically dominant phototroph assimilates phosphorus (P) at significant rat
57 t or dark conditions, focusing on changes in phototroph, bacterial and fungal communities at the soil
58 eria and fungi, with phototrophic organisms (phototrophs) being generally overlooked.
59                  Known planktonic anoxygenic phototrophs belong to only a few restricted groups withi
60 terrestrial and marine environments in which phototrophs benefit from enrichment at the expense of th
61 ent examples that reflect recent advances in phototroph biology as a result of insights from genome a
62 n donor to the reaction center in anoxygenic phototrophs but can also be involved in aerobic respirat
63                         This work shows that phototrophs can directly use solid-phase conductive subs
64 f pigments is characteristic of the obligate phototrophs Chlorobium phaeobacteroides and C. phaeovibr
65 ' (Syn OS-B') and the filamentous anoxygenic phototroph Chloroflexus MS-CIW-1 (Chfl MS-1).
66                                  In oxygenic phototrophs, chlorophylls, hemes, and bilins are synthes
67 crocosms suggesting that light can influence phototroph community structure even in the underlying bu
68 tionized our understanding of early oxygenic phototrophs, complementing and dramatically extending in
69                                  This purple phototroph contains PufX, a polypeptide crucial for dime
70 kely implied that eukaryotic algae and other phototrophs could be the primary producers within the ma
71 lusive and paradoxical, in that, as oxygenic phototrophs, cyanobacteria tend to alkalinize their surr
72 novel rubrerythrin variant from the oxygenic phototroph Cyanophora paradoxa, at 1.20-1.40 A resolutio
73 y, heterotroph identity, their dependence on phototroph-derived C and the type of nutrient enrichment
74 eliance of microbial heterotrophs on biofilm phototroph-derived organic matter under high light avail
75 uggest that stable fungal association with a phototroph does not in itself result in fungal CAZyme lo
76 ongs to the phylum of filamentous anoxygenic phototrophs, does not contain a cytochrome bc or bf type
77                                Biocrusts are phototroph-driven communities inhabiting arid soil surfa
78      On the basis of the breadth of oxygenic phototrophs examined in this study, we conclude that O(2
79                           Eukaryotic complex phototrophs exhibit a colorful evolutionary history.
80                                              Phototrophs export carbohydrates to the fungus, which co
81 i is a niche-adapted, filamentous anoxygenic phototroph (FAP) that lacks chlorosomes, the dominant an
82 a (GSB) and the green filamentous anoxygenic phototrophs (FAPs).
83  95% of carbon from photosynthesis) acquired phototrophs form blooms.
84 nt et al. have discovered a new thermophilic phototroph from a poorly characterized bacterial phylum
85 e may not predict patterns of metal usage by phototrophs from freshwater and terrestrial habitats.
86                            Here, we isolated phototrophs from Mn removal beds in Pennsylvania, USA, i
87 mical analyses suggest that light stimulates phototroph growth, which may directly and/or indirectly
88                                 In contrast, phototrophs had the greatest niche breadth and formed so
89                                     Oxygenic phototrophs have played a fundamental role in Earth's hi
90 ate assimilation in methylotrophs and purple phototrophs have revealed remarkable and complex new pat
91 dimeric reaction center-photosystem from the phototroph Heliobacterium modesticaldum exhibits perfect
92 chococcus-Roseobacter interaction as a model phototroph-heterotroph case study, we show that although
93            Here, we have performed long-term phototroph-heterotroph co-culture experiments under nutr
94                                    Microbial phototroph-heterotroph interactions propel the engine th
95  the molecular processes underpinning marine phototroph-heterotroph interactions.
96  that 2-MeBHPs are produced by an anoxygenic phototroph, however, challenged both their taxonomic lin
97  Prochlorococcus is the numerically dominant phototroph in the oligotrophic oceans.
98  Prochlorococcus is the numerically dominant phototroph in the tropical and subtropical oceans, accou
99 ium Prochlorococcus is the dominant oxygenic phototroph in the tropical and subtropical regions of th
100 thesis), their co-occurrence with anoxygenic phototrophs in a variety of environments and their persi
101                                              Phototrophs in ikaite thus thrive in polymer-bound endol
102  and Synechococcus, the numerically dominant phototrophs in ocean ecosystems.
103 ive oxygen species generated by the abundant phototrophs in the eutrophic PRE.
104 odophytan order Cyanidiales are unique among phototrophs in their ability to live in extremely low pH
105                                              Phototrophs, in turn, benefit from fungal protection fro
106 usually invoked to account for fossil marine phototrophs, including macroscopic multicellular eukaryo
107 me-based insights into the transition from a phototroph into a secondary heterotroph have so far only
108  center (LH1-RC) core complex of this purple phototroph is characterized by the co-existence of monom
109 re by our similarity-based comparisons among phototrophs is our lack of knowledge what ion transporte
110 taxonomic identity of these early anoxygenic phototrophs is uncertain, including whether or not they
111 g in cyanobacteria and only a few eukaryotic phototrophs, JSC1_58120g3's far-red absorption arises fr
112                                    Microbial phototrophs, key primary producers on Earth, use H2O, H2
113 ndance over sulfate reducers, and anoxygenic phototrophs largely outnumbered oxygenic photoautotrophs
114                      The bioinspiration from phototrophs, light-harvesting antennas, chlorophylls, an
115 cycle has been well characterized in various phototrophs, little is known about the cellular signalin
116 ns concerning the early Earth is how ancient phototrophs made the evolutionary transition from anoxyg
117 systems, and suggest that blooms of oxygenic phototrophs modulated the recovery from the most negativ
118 of key functional groups (chemoheterotrophs, phototrophs, nitrogen fixers, denitrifiers, sulfate redu
119 cus and Synechococcus, the two most abundant phototrophs on Earth, thrive in oligotrophic oceanic reg
120 ersity, and biology of the two most abundant phototrophs on Earth.
121 eria are the most abundant oxygen-generating phototrophs on our planet and are therefore important to
122               In marine ecosystems, acquired phototrophs - organisms that obtain their photosynthetic
123 sence of many Phytophthora genes of probable phototroph origin supports a photosynthetic ancestry for
124         CcdA-null mutants of the facultative phototroph Rhodobacter capsulatus are unable to grow und
125 or formaldehyde oxidation in the facultative phototroph Rhodobacter sphaeroides has allowed the ident
126 of the photosynthetic membrane of the purple phototroph Rhodobacter sphaeroides has been characterise
127 e role of a gene (rpoH) from the facultative phototroph Rhodobacter sphaeroides that encodes a protei
128                               The anoxygenic phototroph Rhodobacter sphaeroides uses 3-hydroxypropion
129  of 2-MeBHP in two strains of the anoxygenic phototroph Rhodopseudomonas palustris.
130            Here, we developed the anoxygenic phototroph, Rhodopseudomonas palustris, as a biocatalyst
131                      Many organisms, notably phototrophs, routinely acquire resources over only a fra
132 particularly by methylotrophs and anoxygenic phototrophs, should be further studied and incorporated
133                                  Facultative phototrophs such as Rhodobacter sphaeroides can switch b
134 xolimnion communities replaced by anoxygenic phototrophs, sulfate-reducing bacteria and SAR406 in the
135 CC 7942, is a genetically tractable obligate phototroph that is being developed for the bioproduction
136 ar to be the only known anaerobic anoxygenic phototrophs that are not capable of autotrophy.
137 n order to examine the resilience of benthic phototrophs that are pivotal to coastal ecosystem functi
138 trast, heterotrophs and mixotrophic acquired phototrophs (that obtain < 30% of their carbon from phot
139 e nutritional flexibility of many anoxygenic phototrophs, the complete genome sequence of H. modestic
140 ction is not solely associated with obligate phototrophs, the process need not be confined to the pho
141 ia but negatively in eukaryotes, whereas for phototrophs, the scaling is negligible for cyanobacteria
142                                           As phototrophs they contribute to photosynthetic C fixation
143                  As versatile and ubiquitous phototrophs, they are used as models for oxygenic photos
144                               The ability of phototrophs to convert light into biological energy is c
145 s to produce superoxide, the contribution of phototrophs to Mn(II) oxidation in the environment may b
146        Given the known widespread ability of phototrophs to produce superoxide, the contribution of p
147 onships, central to which are a fungus and a phototroph, typically an alga and/or cyanobacterium.
148 ssfully constructed a synthetic community of phototrophs using Rhodopseudomonas palustris (R. palustr
149 lore the potential for light sensing in this phototroph, we measured its global gene expression patte
150 blages, indicating that the newly identified phototrophs were photosynthetically competent.
151 se pairs, 1,716 genes) of any known oxygenic phototroph, whereas the genome of its low-light-adapted
152 action centers would have provided primitive phototrophs with an environmental advantage before the e
153      Integration of DNA derived from ancient phototrophs with their characteristic lipid biomarkers h
154 ten dominated by unicellular and filamentous phototrophs within an exopolymer matrix.
155 n, and photosynthetic activity of endolithic phototrophs within the porous ikaite crystal matrix.

 
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