ライフサイエンスコーパス: endophytic

1 ve to PGBP-free controls while the extent of endophytic accumulation depended on the colonization mod

2 mesophyll region of host leaves occurs, but endophytic and epiphytic bacterial growths are not corre

3 ccurring microbial communities contribute to endophytic and epiphytic colonization.

4 and Dazzle respectively, and much higher in endophytic and tightly bound cells than in epiphytic and

5 tequilana leaves after inoculation of their endophytic bacteria (Enterobacter cloacae).

6 he combination of native pollutant-degrading endophytic bacteria and fast-growing poplar tree systems

7 ly, we found the genomes of rhizospheric and endophytic bacteria associated with S. salsa to be enric

8 Non-plant pathogenic endophytic bacteria can promote plant growth, improve ni

9 In particular, the endophytic bacteria H. seropedicae showed strong epiphyt

10 necessary for this interior colonization in endophytic bacteria have been identified.

11 The genomes of four endophytic bacteria now available should promote discove

12 information is available on the influence of endophytic bacteria on phytoremediation of widespread en

13 colonization of plants we demonstrated that endophytic bacteria potentially transfer more nitrogen t

14 present evidence showing nitrogen flow from endophytic bacteria to plants in a process that appears

15 Plants form symbiotic associations with endophytic bacteria within tissues of leaves, stems, and

16 ene transfer into neighboring plant species, endophytic bacteria, and mycorrhizal fungi.

17 her or how plants obtain nitrogen from these endophytic bacteria.

18 oplastic water potential is a determinant of endophytic bacterial population size, and water stress,

19 al structure of a PRF from the Gram-negative endophytic bacterium Burkholderia phytofirmans The cryst

20 aspirillum seropedicae is a diazotrophic and endophytic bacterium that associates with economically i

21 The extent of endophytic colonization by strains is regulated by plant

22 t to assess nitrogen absorbed as a result of endophytic colonization of plants we demonstrated that e

23 a H. seropedicae showed strong epiphytic and endophytic colonization of roots.

24 ay have been co-opted from genes involved in endophytic colonization.

25 ted humidity-dependent dyshomeostasis of the endophytic commensal bacterial community in the phyllosp

26 e more modular than ectomycorrhizal and root endophytic communities, with arbuscular mycorrhizal fung

27 e (immediately surrounding the root) and the endophytic compartment (within the root) contribute to p

28 Our rigorous definition of an endophytic compartment microbiome should facilitate cont

29 the hypotheses that the root rhizosphere and endophytic compartment microbiota of plants grown under

30 Endophytic compartments from both soils feature overlapp

31 y distinct bulk soils and in rhizosphere and endophytic compartments prepared from roots grown in the

32 tive endophyte bacterial isolate library for endophytic competency.

33 beneficial associations with associative and endophytic diazotrophic bacteria.

34 antifungal activities against saprotrophic, endophytic, entomopathogenic, and garden-pathogenic fung

35 he precise studies on evolutionary origin of endophytic Epichloe species, their coevolution with host

36 We surveyed endophytic fungal communities in leaves of a single tree

37 Muscodor is a novel endophytic fungal genus that produces bioactive volatile

38 larity among different mycorrhizal types and endophytic fungal guilds.

39 of the currently characterized antagonistic endophytic fungi and their effects on nematode behavior

40 Endophytic fungi are found within the roots of healthy p

41 are consistent with suggestions that foliar endophytic fungi are hyperdiverse.

42 sition, diversity, and dispersal patterns of endophytic fungi associated with needles of Pinus taeda

43 Colonization of plants by particular endophytic fungi can provide plants with improved defens

44 In part, this may be caused by the fact that endophytic fungi form a rather heterogeneous group.

45 Endophytic fungi have been reported from many plants and

46 The application of enzymes from endophytic fungi in constructing biosensors broadens the

47 Endophytic fungi live asymptomatically within plants.

48 The endophytic fungi of woody plants may be diverse as often

49 A new study sheds light on why endophytic fungi that live inside Yew trees also make th

50 Every plant species examined to date harbors endophytic fungi within its asymptomatic aerial tissues,

51 r pest management include the application of endophytic fungi, such as Trichoderma harzianum, that ac

52 l approach to mine the chemical diversity of endophytic fungi.

53 es A-E, isolated from a culture broth of the endophytic fungus Curvularia geniculata, is described.

54 ucted by physical adsorption of the isolated endophytic fungus Eupenicillium shearii FREI-39 esterase

55 he mechanism of action of Muscodor albus, an endophytic fungus known for its volatile antimicrobial a

56 produced by an indeterminate species of the endophytic fungus Nodulisporium.

57 om the fermentation broth of an unidentified endophytic fungus obtained from the bark of Ficus microc

58 S-based metabolomic analysis of the Hawaiian endophytic fungus Paraphaeosphaeria neglecta FT462 led t

59 ay of spiro compounds, and an extract of the endophytic fungus Penicillum namyslowski, containing gri

60 The root endophytic fungus Piriformospora indica enhances plant a

61 discovered a novel compound isolated from an endophytic fungus that inhibits fungal sphingolipid synt

62 ogen-fixing symbiont, the plants harbored an endophytic fungus that produced elemental Se.

63 at, under phosphate-limiting conditions, the endophytic fungus, Colletotrichum tofieldiae, provides g

64 dial pigmentation and development in a plant endophytic fungus, Pestalotiopsis fici.

65 cing of Calcarisporium arbuscula, a mushroom-endophytic fungus, revealed 68 core genes that are invol

66 nt membrane architecture favoring epithelial endophytic growth into the dermis and accelerating invas

67 This is especially true for Rafflesia, an endophytic holoparasite that produces the largest flower

68 M32-eGFP that binds to the chitosan exposing endophytic infection structures of Puccinia graminis f.

69 viding strong evidence of the ability of the endophytic inoculated trees to effectively remove TCE fr

70 Complex renal tumors, such as hilar and endophytic lesions, have also been performed robotically

71 of insect pathogenesis while maintaining an endophytic lifestyle and provide examples of genes that

72 Genome analysis revealed a link between its endophytic lifestyle and the expansion of its repertoire

73 itation may degrade and obtain nitrogen from endophytic microbes.

74 In addition, endophytic microbiota and the manifold interactions betw

75 Endophytic microorganisms exist within the living tissue

76 Similarly, neither endophytic Mycosphaerella nor endophytic Rhizosphaera is

77 the performance of the radius, exophytic or endophytic, nearness to collecting system or sinus, ante

78 sions that progressed to malignancy, 12 were endophytic (P = .02).

79 at benign tumors converted from exophytic to endophytic papillomas before progressing to carcinomas.

80 The endophytic parasites Rafflesiaceae are placed in the div

81 parasitoid wasps are descendants of a single endophytic parasitoid ancestor that lived around 247 mya

82 oots (rhizospheric) or within plant tissues (endophytic), play an active role in modulating ethylene

83 ntaminated media (400 mg kg(-1) Zn) with the endophytic Pseudomonas brassicacearum and rhizospheric R

84 larly, neither endophytic Mycosphaerella nor endophytic Rhizosphaera isolates were most closely relat

85 s where it arrested biotrophic growth of the endophytic S. reilianum.

86 Epichloe spp. are naturally occurring fungal endophytic symbionts of many cool-season grasses.

87 ty of microbial interactions associated with endophytic systems.

88 In common, both associative and endophytic types of colonization can result in beneficia