ライフサイエンスコーパス: autotrophy

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1 onate is not known to be a direct source for autotrophy.

2 oxygenic phototrophs that are not capable of autotrophy.

3 that minerals could directly supply CO2 for autotrophy.

4 c signatures consistent with mineral-sourced autotrophy.

5 opmental program that promotes the switch to autotrophy.

6 t the dominant metabolism at depth indeed is autotrophy (83%), whereas heterotrophic consumption of m

7 DH dehydrogenase genes, as well as genes for autotrophy and aromatic compound degradation.

8 stoichiometry, relative to a system in which autotrophy and heterotrophy are mutually exclusive.

9 Restoration of autotrophy and leaf pigmentation following aadA-based tr

10 us maintaining favourable conditions for net autotrophy at the hole floors.

11 developing seedling must reach the state of autotrophy before the nutrients stored in the seed are e

12 n its source (mine tailings) and metabolism (autotrophy) from those of previous studies.

13 explored, and the ecological implications of autotrophy in attine ant- and plant root-associated Pseu

14 In this study, we examined autotrophy in Pseudonocardia dioxanivorans CB1190, which

15 drive the shift between net heterotrophy and autotrophy in the oligotrophic ocean.

16 may have for the organism in the context of autotrophy in the RNA world.

17 est that it results in remarkably robust net autotrophy on the Greenland Ice Sheet.

18 ained by differences in trophic preferences (autotrophy or heterotrophy).

19 Either to sustain autotrophy, or as a prelude to heterotrophy, organic syn

20 ional constraints during the transition from autotrophy to a nonphotosynthetic parasitic lifestyle.

21 sion support heterotrophy, which succumbs to autotrophy under groundwater discharge.

22 , at some point, must make the transition to autotrophy via the initiation of photosynthesis.

23 lysis of cells grown under strict H(2)-CO(2) autotrophy was consistent with the involvement of Msed_0

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