ライフサイエンスコーパス: extracellular enzyme

1 tivity than known natural substrates of this extracellular enzyme.

2 hyton and the activities of two of the three extracellular enzymes.

3 iration potential, and the activity of three extracellular enzymes.

4 nments may be subjected to biodegradation by extracellular enzymes.

5 r the synthesis of secondary metabolites and extracellular enzymes.

6 and rsmB control the expression of genes for extracellular enzymes.

7 etion that is protein kinase C-mediated, and extracellular enzyme activation.

8 place on metallic surfaces and the impact of extracellular enzymes, active within the biofilm matrix,

9 organic matter (DOM) composition on aquatic extracellular enzyme activities (EEAs) in waters drainin

10 orest exposed to elevated CO(2) by measuring extracellular enzyme activities at soil microsites acces

11 Furthermore, extracellular enzyme activities correlated with nutrient

12 perature sensitivity of the soil CO2 efflux, extracellular enzyme activities, microbial efficiency, a

13 biomass, fungal : bacterial (F : B) ratios, extracellular enzyme activities, soil carbon : nitrogen

14 ed with a community succession and increased extracellular enzyme activities.

15 al transcribed spacer (ITS) copy numbers and extracellular enzyme activity (EEA) potentials were one

16 phospholipid fatty acid analysis (PLFA) and extracellular enzyme activity across a well-replicated,

17 tic rate, net N mineralization and microbial extracellular enzyme activity at multiple locations with

18 nt enzyme inhibitors for selectively imaging extracellular enzyme activity by PET.

19 Extracellular enzyme activity did not differ with forest

20 By contrast, soil extracellular enzyme activity is highly convergent acros

21 bioavailability was associated with elevated extracellular enzyme activity of the initial microbial c

22 d protease IV gene had significantly greater extracellular enzyme activity than P. aeruginosa.

23 obial community structure and diversity, and extracellular enzyme activity.

24 ed on B. intestinalis, it is likely that the extracellular enzymes also release nutrients to members

25 Autotaxin (ATX) is an extracellular enzyme and an autocrine motility factor th

26 that activates RsmA production and represses extracellular enzyme and harpin(Ecc) production, rsmB tr

27 OHL controls extracellular enzyme and HarpinEcc production.

28 the expression of various traits, including extracellular enzyme and protein production and pathogen

29 are impaired in the secretion of a range of extracellular enzymes and accumulate abnormal Golgi-like

30 Secretion of extracellular enzymes and adhesion molecules from subapi

31 However, little is known about extracellular enzymes and aquatic microorganisms involve

32 act positively to regulate the synthesis of extracellular enzymes and EPS, but that RpfC acts negati

33 The synthesis of extracellular enzymes and extracellular polysaccharide (

34 This mutant also had reduced levels of extracellular enzymes and extracellular polysaccharide (

35 rients as key triggers for the expression of extracellular enzymes and metabolites directly controlle

36 including antibiotics), entrapment of useful extracellular enzymes and nutrients, as well as opportun

37 functions as a global negative regulator of extracellular enzymes and proteins and secondary metabol

38 d rpf genes cause downregulated synthesis of extracellular enzymes and reduced virulence of Xanthomon

39 ular organisms, acting as structural matrix, extracellular enzymes, and signal molecules.

40 These extracellular enzymes are synthesized as preproenzymes c

41 i and bacteria with shotgun metagenomics and extracellular enzyme assays.

42 salinity on the activity of carbon-degrading extracellular enzymes (beta-1, 4-glucosidase, 1, 4-beta-

43 phosphatase may have applicability to other extracellular enzymes but remains to be established.

44 ion and release of lipolytic and proteolytic extracellular enzymes by P. acnes were shown to increase

45 erial activity of PLA2, suggesting that this extracellular enzyme can substantially penetrate dense b

46 receptors are combined with the plethora of extracellular enzymes capable of manipulating extracellu

47 e through a mechanism that is independent of extracellular enzyme concentration.

48 Lysyl oxidase is an extracellular enzyme critical for the normal biosynthesi

49 eroxide dismutase (EC-SOD) is the only known extracellular enzyme designed to scavenge the superoxide

50 lycosidic bonds in pectin, and are important extracellular enzymes for both pathogenic and saprotroph

51 n has also been focused on the exocytosis of extracellular enzymes from hyphal tips.

52 ia isolates suggests a potential role of the extracellular enzyme in substrate degradation relevant t

53 aches to measure the activities of microbial extracellular enzymes in aquatic environments are hamper

54 Alkaline phosphatases are ubiquitous extracellular enzymes in aquatic systems and play a cent

55 deleted fails to cause overproduction of the extracellular enzymes in Ecc71.

56 any lineage of ECM fungi actively expresses extracellular enzymes in order to degrade SOM and transf

57 ere fungal mycelium is too sparse to produce extracellular enzymes in sufficient quantities to detoxi

58 eflecting a biological role of keeping these extracellular enzymes inactive until secretion.

59 are responsible for the delivery of soluble extracellular enzymes into the surrounding medium, or fo

60 Thus, the extracellular enzyme is a potential virulence factor in

61 by kallikrein-related peptidase 6 (KLK6), an extracellular enzyme known to cleave recombinant alpha-s

62 However, the soil microbial extracellular enzymes leucine amino peptidase and phosph

63 ever, these suspensions inhibited one of the extracellular enzymes (leucine aminopeptidase), pointing

64 ports the hypothesis that the RpoS effect on extracellular enzyme levels, hrpNEcc expression, and vir

65 rs as previously unrecognized targets of the extracellular enzyme lysyl oxidase (LOX), the level of w

66 ng required for threat learning involves the extracellular enzyme matrix metalloproteinase (MMP) 9.

67 eus suggests that even small amounts of this extracellular enzyme mobilized early in inflammation cou

68 in ECM soils shifted to higher investment in extracellular enzymes needed for nitrogen and phosphorus

69 Here, we show that the activity of two extracellular enzymes of intact heterotrophic biofilms,

70 itated in vivo following their hydrolysis by extracellular enzymes overexpressed by cancer cells.

71 us studies have shown that the production of extracellular enzymes (pectate lyase [Pel], polygalactur

72 condary variant, including the production of extracellular enzymes, pigments, antibiotics and light.

73 Extracellular enzymes play critical roles on the degrada

74 onucleases Sa, Sa2, and Sa3 are three small, extracellular enzymes produced by different strains of S

75 teractions vary with community investment in extracellular enzyme production and the magnitude of tra

76 We conclude that KdgREcc affects extracellular enzyme production by two ways: (i) directl

77 to the flhDC operon of E. coli also controls extracellular enzyme production.

78 epH, on the other hand, positively regulates extracellular enzyme production.

79 the expression of various traits, including extracellular enzyme/protein production and pathogenicit

80 The transcription of the genes for two extracellular enzymes (prtA, encoding a serine protease,

81 proteins, zinc finger protein, intracellular/extracellular enzymes, structural proteins, anti-stress/

82 otovora strain 71 (hereafter Ecc71) produces extracellular enzymes such as pectate lyase isozymes (Pe

83 Extracellular enzyme systems for the metabolism of polys

84 transcriptome, and secretome revealed unique extracellular enzyme systems, including an unusual reper

85 e data provide new information about a novel extracellular enzyme that participates in GAS-human inte

86 ve retained the genetic potential to produce extracellular enzymes that degrade SOM, calling into que

87 ith inhibition of matrix metalloproteinases, extracellular enzymes that generate integrin ligands.

88 E-NTPDases are extracellular enzymes that hydrolyze nucleotides.

89 we examined the levels of intracellular and extracellular enzymes that proteolytically cleave proBDN

90 riments with Vibrio cholerae, which secretes extracellular enzymes to digest its primary food source,

91 viduals need to donate public goods, such as extracellular enzymes), virulence is predicted to increa

92 Multifunctionality, based on extracellular enzymes, was highest under high light cond

93 n, or by overexpression of 6-O sulfatase, an extracellular enzyme which removes 6-O sulfate groups wi

94 Impairment of extracellular enzymes which mediate the uptake of nutrie

95 metalloproteinases (MMPs), a large family of extracellular enzymes with proteolytic activities that p