ライフサイエンスコーパス: photoheterotrophic

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

17 Under photoheterotrophic conditions, however, CheW3 is require

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

19 chemotactic responses under both aerobic and photoheterotrophic conditions.

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

21 Under photoheterotrophic growth conditions, coordinate control

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

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

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

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

26 This preference for photoheterotrophic growth has interesting implications f

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

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

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

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

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

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

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

34 For photoheterotrophic growth, a Chlamydomonas reinhardtii c

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

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

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

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

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

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

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

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

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

44 Photoheterotrophic metabolism of two meta-hydroxy-aromat

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

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

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

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

49 Using an obligate photoheterotrophic mutant that carries a short deletion

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

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

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