ライフサイエンスコーパス: photoheterotrophic

1 (RNAP) to investigate rRNA synthesis in the photoheterotrophic alpha-proteobacterium Rhodobacter sph

2 ized to the poles of the cell under aerobic, photoheterotrophic and anaerobic dark conditions, demons

3 and cbbM genes, respectively, could support photoheterotrophic and autotrophic growth.

4 phototrophic and heterotrophic protists, and photoheterotrophic and copiotrophic bacteria.

5 sion in predicting metabolic changes between photoheterotrophic and photoautotrophic conditions.

6 latus and Rhodobacter sphaeroides under both photoheterotrophic and photoautotrophic growth condition

7 ems, were probed in strains grown under both photoheterotrophic and photoautotrophic growth condition

8 h R. capsulatus maintains redox poise during photoheterotrophic and photoautotrophic growth.

9 hic modes, i.e., autotrophic, heterotrophic, photoheterotrophic, and mixotrophic modes.

10 Photoheterotrophic bacteria harvest light energy using e

11 Rhodobacter sphaeroides is a free-living, photoheterotrophic bacterium known for its genomic and m

12 ression upon transition of the facultatively photoheterotrophic bacterium Rhodobacter sphaeroides 2.4

13 ies of anaerobic benzoate degradation by the photoheterotrophic bacterium Rhodopseudomonas palustris.

14 odobacter sphaeroides 2.4.1 is a facultative photoheterotrophic bacterium with tremendous metabolic d

15 ltandhD1/D2) mutant was unable to grow under photoheterotrophic conditions and exhibited low respirat

16 ound to be derepressed in strain 16PHC under photoheterotrophic conditions in the presence of ammonia

17 nitrogen sources under chemoheterotrophic or photoheterotrophic conditions remain unknown.

18 f the DeltabluB strain observed under anoxic photoheterotrophic conditions was corrected by the addit

19 on of cheW2 and cheA2 under both aerobic and photoheterotrophic conditions, and cheW3 under photohete

20 otoheterotrophic conditions, and cheW3 under photoheterotrophic conditions, disrupts the cluster and

21 inimal medium, is high light-sensitive under photoheterotrophic conditions, has lower accumulation of

22 Under photoheterotrophic conditions, however, CheW3 is require

23 Under photoheterotrophic conditions, R. palustris prioritizes

24 chemotactic responses under both aerobic and photoheterotrophic conditions.

25 ty and highly reduced abundance of PSI under photoheterotrophic conditions.

26 pression was repressed in strain 16PHC under photoheterotrophic growth conditions with either ammonia

27 Under photoheterotrophic growth conditions, coordinate control

28 These findings indicate that, under photoheterotrophic growth conditions, R. palustris can d

29 ded as a sole source of organic carbon under photoheterotrophic growth conditions.

30 derepressed in the presence of ammonia under photoheterotrophic growth conditions.

31 The disruption of Mic60 and Orf52 caused photoheterotrophic growth defects, which are most severe

32 wherein disrupting RubisCO activity prevents photoheterotrophic growth due to the accumulation of tox

33 This preference for photoheterotrophic growth has interesting implications f

34 techuate was the sole organic carbon source, photoheterotrophic growth in R. palustris was slow relat

35 bb(I) and cbb(II) promoter activities during photoheterotrophic growth in the presence of dimethyl su

36 bility of glycolate, CO2, or DMSO to support photoheterotrophic growth of CT01 suggests that one or m

37 found that exogenous glycolate also rescued photoheterotrophic growth of CT01, leading us to propose

38 During photoheterotrophic growth on organic substrates, purple

39 wherein the Calvin cycle is necessary during photoheterotrophic growth to maintain a pool of oxidized

40 bisphosphate carboxylase (RubisCO), prevents photoheterotrophic growth unless an electron acceptor is

41 cteria because of its capacity for anaerobic photoheterotrophic growth using aromatic acids.

42 For photoheterotrophic growth, a Chlamydomonas reinhardtii c

43 ion was not affected by cco mutations during photoheterotrophic growth, suggesting that differences e

44 hat requires an exogenous electron donor for photoheterotrophic growth, transcription of the genes of

45 sources during mixotrophy allows a switch to photoheterotrophic growth, where the photosynthetic appa

46 g exposure to dark and blue light and during photoheterotrophic growth.

47 s, such as malate, into cell material during photoheterotrophic growth.

48 aerobic (chemoheterotrophic) and anaerobic (photoheterotrophic) growth conditions has not been obser

49 ilities observed across archaeal lineages: a photoheterotrophic halophile (Halobacterium salinarum NR

50 eon, Candidatus Nanopetramus SG9, revealed a photoheterotrophic life style and a low median isoelectr

51 om around the world, and evidence supports a photoheterotrophic lifestyle combining phototrophy via p

52 or at least 40% of total ATP generation from photoheterotrophic metabolism (without considering maint

53 Photoheterotrophic metabolism of R. palustris is primari

54 Photoheterotrophic metabolism of two meta-hydroxy-aromat

55 Synechocystis sp. PCC 6803 employs a unique photoheterotrophic metabolism.

56 cyanobacterium Synechocystis sp. PCC 6803, a photoheterotrophic model organism for the study of photo

57 NA mixture was used to transform an obligate photoheterotrophic mutant (Y161W) of the cyanobacterium

58 Starting from an obligate photoheterotrophic mutant lacking the T271-K277 region,

59 Using an obligate photoheterotrophic mutant that carries a short deletion

60 rium Synechocystis sp. PCC 6803, an obligate photoheterotrophic mutant was isolated that contained th

61 d for functional complementation of obligate photoheterotrophic mutants carrying a deletion in one su

62 maintain cell viability in dominant coastal photoheterotrophic oligotrophs while promoting the growt

63 y complexes, FtsZ and MreB in aerobic and in photoheterotrophic R. sphaeroides cells using fluorescen

64 metabolic effects of light on environmental photoheterotrophic taxa.