ライフサイエンスコーパス: phyllosphere

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1 important step in bacterial infection of the phyllosphere.

2 ophytic commensal bacterial community in the phyllosphere.

3 ntibiotics or competing for nutrients in the phyllosphere.

4 isease epidemiology, and microbiology of the phyllosphere.

5 h the exception of the rspC promoter) in the phyllosphere.

6 dual E. herbicola cells as they colonize the phyllosphere.

7 these sugars to microbial colonizers of the phyllosphere.

8 by its requirement for growth of Pss in the phyllosphere.

9 l importance of bacterial communities in the phyllosphere and rhizosphere of plants, a more detailed

10 rhizosphere was the opposite to that in the phyllosphere, and the higher number and activity of E. c

11 ributes that drive community assembly in the phyllosphere are poorly understood.

12 Phyllosphere bacteria were identified from Citrus sinesi

13 es had 97--100% similarity to those of known phyllosphere bacteria, but only two of them matched thos

14 trains that had been described previously as phyllosphere bacteria.

15 Phyllosphere bacterial communities have the potential to

16 These correlations between phyllosphere bacterial diversity and host growth, mortal

17 nceptual framework for understanding diverse phyllosphere-bacterial interactions.

18 tant role in enabling Pss to flourish in the phyllosphere, but not the spermosphere.

19 on their surfaces and in the rhizosphere and phyllosphere by a multitude of different microorganisms

20 gi in nutrient-limited environments like the phyllosphere by the novel mechanism of HI induction.

21 Like other studied ecosystems, microbial phyllosphere communities therefore are more complex than

22 ne dehalogenase cmuA gene in the A. thaliana phyllosphere correlated with HOL1 genotype, as shown by

23 If metabolic activity in the phyllosphere corresponds to a more prepared state of inf

24 us extra-leaf processes to the generation of phyllosphere dynamics is important to determining the ra

25 ated with aboveground tissues, termed 'plant-phyllosphere feedback (PPFs)'.

26 , we tested the combined effects of soil and phyllosphere feedback under field conditions.

27 of rulAB for survival of P. syringae in its phyllosphere habitat, coupled with its wide distribution

28 However, phyllosphere (i.e., leaf) population sizes of the hrcC a

29 from a variety of environments including the phyllosphere, i.e. the aerial parts of vegetation.

30 ecting the above-ground parts of plants (the phyllosphere) in crop fields and natural ecosystems, but

31 Extension of the PSF framework to the phyllosphere is needed to more fully elucidate plant-mic

32 ial habitat influenced by plants, termed the phyllosphere, is particularly amenable to studies of mic

33 c and fungal communities in the rhizosphere, phyllosphere, leaf and root endosphere, as well as proxi

34 Phyllosphere microbial communities were evaluated on lea

35 Phyllosphere microbiota differed significantly between p

36 llel greenhouse experiments, rhizosphere and phyllosphere microbiota of con- and heterospecific hosts

37 Our results suggest that phyllosphere microbiota, like rhizosphere microbiota, ca

38 death relative to the population dynamics of phyllosphere microorganisms.

39 AB-induced UV mutability was also tracked in phyllosphere populations of B86-17 for up to 5 days foll

40 es for distinguishing these processes within phyllosphere populations.

41 abundance of CH3Cl-degrading bacteria in the phyllosphere suggests that CH3Cl-degrading bacteria co-d

42 Because of water limitations on phyllosphere surfaces, bacterial colonists, including pa

43 The phyllosphere--the aerial surfaces of plants, including l

44 Bacterial communities in the phyllosphere were dominated by a core microbiome of taxa

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