ライフサイエンスコーパス: heterotroph

1 een demonstrated in marine and soil-dwelling heterotrophs.

2 and establishment of non-photosynthetic myco-heterotrophs.

3 ately drives diverse assemblages of seafloor heterotrophs.

4 oleum constituents were dominated by aerobic heterotrophs.

5 ted by H(2) syntrophy with hyperthermophilic heterotrophs.

6 which suggests that these picobiliphytes are heterotrophs.

7 reduced carbon and sulphur by surface ocean heterotrophs.

8 ses of energy acquisition and utilization in heterotrophs.

9 nery; that is, they could have been obligate heterotrophs.

10 rbon from fungi and are thus defined as myco-heterotrophs.

11 fate reducers, and thermophilic fermentative heterotrophs, all consistent with fluid chemistry.

12 lude most major metabolic types of anaerobic heterotrophs and acetogenic bacteria.

13 In contrast, heterotrophs and mixotrophic acquired phototrophs (that

14 was abundant in high DO and pH and contained heterotrophs and oxidizers of iron, nitrite, and ammoniu

15 observed in marine photoautotrophs and soil heterotrophs, and similar flexibility in phosphorus sour

16 We propose that heterotrophs (animals and fungi) are able to sense chemi

17 oaccumulates from plants to predators; thus, heterotrophs are Na-rich sources.

18 t-in and were likely caused by common marine heterotrophs associated with degradation of high-molecul

19 We unveiled a diverse microbial community of heterotrophs, autotrophs, predators, and symbionts, a co

20 Heterotroph biomass on leaves, MeHg in leaves, and MeHg

21 hich is thought of as primarily a cellulosic heterotroph but is shown here to be endowed with the abi

22 vity of ammonia-oxidizing bacteria (AOB) and heterotrophs but not nitrite-oxidizing bacteria.

23 thermoacidophilic sulphur- or iron-reducing heterotroph capable of growing from pH 3.3 to 5.8 and be

24 hs, some methanotrophs, and to our surprise, heterotrophs capable of anaerobic degradation of aromati

25 ium sulfate reactor contained nitrifiers and heterotrophs capable of nitrate reduction.

26 oseobacter interaction as a model phototroph-heterotroph case study, we show that although Synechococ

27 of multiple substrate utilizers rather than heterotrophs characterized by an r-strategist growth reg

28 Here, we have performed long-term phototroph-heterotroph co-culture experiments under nutrient-amende

29 e general belief that marine phototrophs and heterotrophs compete for the same scarce nutrients and n

30 OD was also consumed during the process, but heterotrophs could not outcompete anammox bacteria.

31 he Tenacibaculum-like as free-living aerobic heterotroph, densely colonizing the mesogleal axis insid

32 In contrast, the heterotrophs did not cycle diurnally.

33 s might have a lower nutritive value to soil heterotrophs during the initial stages of litter decompo

34 suggest that oral chloroflexi are anaerobic heterotrophs, encoding abundant carbohydrate transport a

35 integration, the chimera, an amitochondriate heterotroph, evolved.

36 acteria that compete fiercely with algae and heterotrophs for the element.

37 It is a marine heterotroph found in surface and mesopelagic waters in b

38 As heterotrophs, fungi have evolved a diverse range of mech

39 Because many myco-heterotrophs grow in forests dominated by plants associa

40 In the process some fungus-like heterotrophs have been shown to belong elsewhere, and se

41 Importantly, heterotroph identity, their dependence on phototroph-der

42 Testate amoebae are representative heterotrophs in peatlands [16-18], so their populations

43 Some hyperthermophilic heterotrophs in the genus Thermococcus produce H2 in the

44 Heterotrophs, including a bacterium from a previously un

45 ankton as well as proteorhodopsin-containing heterotrophs, including Pelagibacter, SAR86-cluster Gamm

46 Marine phototroph and heterotroph interactions are vital in maintaining the nu

47 Microbial phototroph-heterotroph interactions propel the engine that results

48 lar processes underpinning marine phototroph-heterotroph interactions.

49 milatory utilisation of autotroph biomass by heterotrophs is a fundamental mechanism for the transfer

50 T. pendens is a sulfur-dependent, anaerobic heterotroph isolated from a solfatara in Iceland.

51 Seven hyperthermophilic heterotrophs isolated from low-temperature diffuse fluid

52 Our results demonstrate that heterotrophs isolated from this unusual environment alte

53 ities of mosses, lichens, cyanobacteria, and heterotrophs living at the soil surface-are fundamental

54 Other heterotrophs may also contribute to scavenging of detrit

55 ion of exopolysaccharide and flocculation of heterotroph-methanogen cellular aggregates.

56 Myco-heterotroph Monotropa hypopitys is a widely spread peren

57 ecificity for these fungi, but for most myco-heterotrophs neither the identity of the fungi nor the s

58 r choline catabolism is widespread in marine heterotrophs of the marine Roseobacter clade (MRC).

59 is suggests a shift in reliance of microbial heterotrophs on biofilm phototroph-derived organic matte

60 ion proteins when grown in the presence of a heterotroph or decrease exposure to prey when grown in t

61 haeal community includes both autotrophs and heterotrophs or is a single population with a uniformly

62 Their association with heterotrophs, preference for particles and resourceful m

63 ecoides and the non-photosynthetic, obligate heterotroph Prototheca wickerhamii.

64 de are derived mainly from bacteria or other heterotrophs rather than from photosynthetic organisms.

65 K-6 is particularly interesting because most heterotrophs rely on the transhydrogenase, the TCA cycle

66 uch in common with the twitching motility of heterotrophs such as Pseudomonas and Myxococcus.

67 exchange mutualisms between phototrophs and heterotrophs, such as plants and mycorrhizal fungi or sy

68 ter being more easily metabolized by aquatic heterotrophs than older, heavily modified material.

69 as more diverse and contained more anaerobic heterotrophs than the January and June: Desulfurella and

70 Pyrococcus furiosus is a strictly anaerobic heterotroph that grows optimally at 100 degrees C by the

71 alophiles (Haloarchaea) are oxygen-respiring heterotrophs that derive from methanogens--strictly anae

72 For organisms that feed on organic food (heterotrophs), the most efficient way to produce energy

73 Facultatively anaerobic heterotrophs, they possess an ancestral form of A-type t

74 ial hydrolytic enzyme candidates used by the heterotroph to cleave organic groups and hydrolase polym

75 gene producing an A(28) tail is an obligate heterotroph to obtain photoautotrophic revertants.

76 thesis and carbon fixation, it relies on the heterotroph to remineralize the inevitably leaked organi

77 zing bacteria were more susceptible than the heterotrophs to Pb toxicity.

78 ating environmental conditions, allowing the heterotrophs to prepare for adversity while conditions a

79 study evaluated the inactivation of in situ heterotrophs, total bacteria as observed by flow cytomet

80 stable-state phase that, in the case of the heterotroph, was caused by a switch in motility attribut

81 As a model for opportunistic bacterial heterotrophs, we demonstrated that Vibrio proliferate in

82 Heterotrophs were not affected by sedimentation.

83 ns, although abundances of hyperthermophilic heterotrophs were relatively high.

84 suggests that Ca. U. copiosus is an aerobic heterotroph with numerous putative amino acid and vitami

85 ns show that these marine archaea are motile heterotrophs with extensive mechanisms for scavenging or