ライフサイエンスコーパス: primary metabolism

1 f secondary metabolites, to the reactions of primary metabolism.

2 eatedly by duplication of a gene involved in primary metabolism.

3 defense are likely mediated independently of primary metabolism.

4 g-opening of a purine heterocycle for use in primary metabolism.

5 lated to energy production, respiration, and primary metabolism.

6 and participates in the regulation of plant primary metabolism.

7 y one or more treatment; 28 were involved in primary metabolism.

8 of histone deacetylases on genes involved in primary metabolism.

9 origins of natural product biosynthesis from primary metabolism.

10 f the essential amino acid leucine, and thus primary metabolism.

11 ncH, -I, and -J and the enzyme homologues of primary metabolism.

12 rotective mechanisms and a downregulation of primary metabolism.

13 ation is the first reported in streptomycete primary metabolism.

14 l CoA:ACP transacylase (MAT), recruited from primary metabolism.

15 g that pungency in placenta is adjusted with primary metabolism.

16 s poorly established, in contrast to that of primary metabolism.

17 lapping functions with ZBTB7A in controlling primary metabolism.

18 lly important for the overall functioning of primary metabolism.

19 sive and requires extensive interaction with primary metabolism.

20 most complex organic rearrangements found in primary metabolism.

21 teoforms, including dozens of key enzymes in primary metabolism.

22 dified with a variety of groups derived from primary metabolism.

23 ysis suggesting that Xpp1 is an activator of primary metabolism.

24 products of monosaccharide autoxidation and primary metabolism.

25 or pravastatin depend on cytochrome P450 for primary metabolism.

26 rage proteins synthesized by the pathways of primary metabolism.

27 ion and focused on the genetic variation for primary metabolism.

28 e less affected by environment than mQTLs of primary metabolism.

29 elated to herbivore-induced changes in plant primary metabolism.

30 antly influence the induced changes in plant primary metabolism.

31 ecting target gene expression and ultimately primary metabolism.

32 binds promoters of genes encoding enzymes of primary metabolism.

33 t herbivory causes numerous changes in plant primary metabolism.

34 id cycle and is central to the regulation of primary metabolism.

35 ss cost, as resources are diverted away from primary metabolism.

36 ynthetic pathway, beginning from products of primary metabolism.

37 en balancing and highlight the robustness of primary metabolism.

38 metabolism, and fewer diterpenes of general (primary) metabolism.

39 ed into 19 categories with highest scores in primary metabolism (17%) and transcription (12%).

40 n numerous physiological processes including primary metabolism, although knowledge about the functio

41 tis elegans uses simple building blocks from primary metabolism and a strategy of modular assembly to

42 ese data imply obligate coordination between primary metabolism and cell division and identify period

43 A), an essential cofactor utilized in ~4% of primary metabolism and central to fatty acid, polyketide

44 ighlights examples of the diversity in plant primary metabolism and discusses how we can utilize thes

45 tus, to produce antimicrobial compounds from primary metabolism and enzymatic promiscuity.

46 and underscores an important linkage between primary metabolism and epigenetic gene regulation.

47 es such as sterols and carotenes are part of primary metabolism and found essentially in all plants.

48 nk the production of a tRNA-modified base to primary metabolism and further clarify the biosynthetic

49 at AsCYP51H10 enzyme has been recruited from primary metabolism and has acquired a different function

50 can reduce the oxidative stress produced by primary metabolism and have excess resources, beyond the

51 underlying biological N-N bond formation in primary metabolism and how the associated reactions are

52 upstream of the cAMP-PKA pathway, influences primary metabolism and hyphal growth, while represses se

53 s and they play numerous functional roles in primary metabolism and in ecological interactions.

54 is necessary to better characterize both the primary metabolism and metabolic regulation of C. acetob

55 logenation, epoxidation, and desaturation in primary metabolism and natural product maturation.

56 ming recognized as major regulators of plant primary metabolism and of other cellular processes.

57 ed immune responses which further influences primary metabolism and plant growth, highlighting the co

58 highlighting the complex interaction between primary metabolism and plant immunity.

59 e has been validated as an essential gene to primary metabolism and presents a target for the identif

60 ger gene set that includes genes involved in primary metabolism and production of other specialized c

61 nover compares with filament growth rate and primary metabolism and provided new insights into the bi

62 mpartmentalized into regions responsible for primary metabolism and reproduction (core genome), and p

63 rk during drought stress, linking changes in primary metabolism and the initiation of stress response

64 -regulation of a series of genes involved in primary metabolism and the phenylpropanoid pathway, and

65 infer the level of global reconfiguration of primary metabolism and the subsequent changes in downstr

66 discuss examples of enzyme recruitment from primary metabolism and the variety of paths taken by dup

67 er understanding of the relationship between primary metabolism and virus infection.

68 oxylation step in both leucine biosynthesis (primary metabolism) and methionine chain elongation of g

69 at SN1 silencing affects cell division, leaf primary metabolism, and cell wall composition in potato

70 er cellular functions such as transcription, primary metabolism, and stress resistance.

71 esis/photorespiration balance and changes in primary metabolism are known, caused by the competitive

72 ed that different pathways involved with the primary metabolism are modulated in glandular trichomes

73 relationships of leaf gas-exchange with leaf primary metabolism are still limited.

74 Many pathways of primary metabolism are substantially conserved within an

75 riacylglycerols (TAGs), which accumulates in primary metabolism, are degraded during stationary phase

76 mix of chemistry that has been adopted from primary metabolism as well as those with no chemical pre

77 genes involved in N uptake and assimilation (primary metabolism) as well as stress response pathways

78 on of a secondary metabolite unessential for primary metabolism but important to change physical prop

79 esize basic metabolites needed for survival (primary metabolism), but different taxa produce distinct

80 synthesis, the pentose phosphate pathway and primary metabolism, but lower levels of defense-related

81 ived from terpene synthase genes involved in primary metabolism by duplication and divergence in stru

82 d for two model systems, liver and adipocyte primary metabolism, by applying an algorithm for top-dow

83 Primary metabolism can be measured by the universally co

84 pectrometry-based profiling of lipidomic and primary metabolism changes in the liver and plasma revea

85 possess a unique diurnal growth pattern and primary metabolism compared with land plants, with highe

86 gnals derived from combinatorial assembly of primary metabolism-derived building blocks, play a centr

87 trong down-regulation of genes implicated in primary metabolism, detoxication apparatus and signal tr

88 in fruit tissue, and study their links with primary metabolism during ripening.

89 but also increases the supply of carbon from primary metabolism, energy and reducing power, which may

90 permit rapid reconstruction and modeling of primary metabolism for all plant genomes in the database

91 In microorganisms, different from primary metabolism for cellular growth, secondary metabo

92 table plant hosts and for further optimizing primary metabolism for sizable production of natural and

93 co-opting the sulphur-delivery machinery of primary metabolism for the biosynthesis of sulphur-conta

94 Isotopic labeling studies of primary metabolism frequently utilize GC/MS to quantify

95 some results were similar, the expression of primary metabolism genes and heat shock proteins was hig

96 Although primary metabolism genes have been retained, the E. webe

97 athway leads to widespread downregulation of primary metabolism genes, an upregulation in virulence f

98 In contrast to most primary metabolism genes, the genes involved in secondar

99 ral metabolism, traditionally referred to as primary metabolism) genes through a detailed study of fe

100 A (CoA) synthase, the homologous enzyme from primary metabolism, HMGS has several differences at the

101 s, and insight into a role for modulation of primary metabolism in betalain synthesis.

102 Compartmentation of primary metabolism in developing embryos poses a signifi

103 dition, we studied the genetic regulation of primary metabolism in dry and imbibed Arabidopsis (Arabi

104 and a shift in resource allocation away from primary metabolism in favor of specialized metabolism.

105 further highlights how genes associated with primary metabolism in nonpathogenic Streptomyces species

106 the genetic factors underlying variation in primary metabolism in potato (Solanum tuberosum), we hav

107 that host plants receive from altering their primary metabolism in response to insect herbivory.

108 resolution proteomics is used to investigate primary metabolism in techniques such as stable isotope

109 play essential roles in enzymes involved in primary metabolism including energy transduction and deo

110 l molecules from modified building blocks of primary metabolism, including an unusual xylopyranose-ba

111 l of plant development, stress response, and primary metabolism, including nutrient homeostasis.

112 suggested, the extent to which autophagy and primary metabolism interact to support plant respiration

113 ndicate that extensive reprogramming of host primary metabolism is a widespread phenomenon among prok

114 However, how primary metabolism is adjusted to fulfill the requiremen

115 sive picture of (13)C distribution along the primary metabolism is elaborated.

116 Although primary metabolism is generally assumed to be conserved,

117 ve transcriptome analysis suggested that the primary metabolism is modulated to augment the supply of

118 Our results revealed that primary metabolism is reconfigured in many ways during T

119 t to other rice studies, the heritability of primary metabolism is similar to Arabidopsis.

120 ependent TRB1 target genes, many involved in primary metabolism, is decreased in the absence of TRB1

121 f these molecules, mostly derived from their primary metabolism, is frequently encoded in metabolic g

122 tral position in oxygenic photosynthesis and primary metabolism - key targets in the complex virulenc

123 corbate, and inositol metabolism, as well as primary metabolisms like amino acid synthesis and glycol

124 ulated whereas for several genes involved in primary metabolism lower expression was detected.

125 pport a link between lignin biosynthesis and primary metabolism mediated by the ammonia released from

126 uinate (secondary metabolism) and shikimate (primary metabolism) metabolic activities are encoded by

127 In plant primary metabolism, metabolic fine-tuning involves feed-

128 grape leaf development to alter patterns of primary metabolism, nutrient mobilization, and defense i

129 study were compared with previous results on primary metabolism obtained from the same material and t

130 ween the two organs, together with shifts in primary metabolism occurring during different periods po

131 ctances, alongside the 53 data profiles from primary metabolism of 14 species grown in different expe

132 Further, several pathways involved in primary metabolism of choline are estrogen-sensitive and

133 formate in a reaction that is crucial to the primary metabolism of many anaerobic bacteria.

134 so worse at reducing the oxidative stress of primary metabolism on glycerol.

135 RV) in order to investigate the influence of primary metabolism on virus infection.

136 ith known functions mostly encode enzymes of primary metabolism or other key biochemical components,

137 ontology analysis for 538 genes involved in primary metabolism, oxidation reduction and response to

138 creasing the expression of genes involved in primary metabolism, phytohormone synthesis and cell divi

139 st hints for coregulation patterns involving primary metabolism plus leaf water and carbon balances t

140 ent with species relationships inferred from primary-metabolism (PM) gene genealogies, and FUM cluste

141 me-dependent protein synthesis and essential primary metabolism processes, such as targeted protein d

142 Primary metabolism provides energy for growth and develo

143 Divergent pathways including primary metabolism, reactive oxygen species response, tr

144 y metabolism despite the potential costs for primary metabolism remain unclear.

145 ids, secondary metabolites whose relation to primary metabolism remains unclear.

146 In addition to the importance of their primary metabolism, some cyanobacteria are prolific prod

147 r evolutionarily constrained counterparts in primary metabolism, specialized metabolic enzymes may be

148 Mutants demonstrate changes in primary metabolism, such as modulation of fatty acid com

149 ne (Cys) is a master control switch of plant primary metabolism that coordinates the flux of sulfur w

150 siological trait by measuring the changes in primary metabolism that occur during the transition in o

151 Apart from a large-scale reconstruction of primary metabolism, the model includes the full known po

152 wledge has existed for sulfur trafficking in primary metabolism, the secondary metabolism involving s

153 ication between organelles and regulation of primary metabolism through redox-mediated signaling are

154 oning, photochemistry and galactolipids) and primary metabolism (through metabolomics) in two natural

155 orial study of multiple transgenes targeting primary metabolism thus offers opportunities to probe th

156 four enzymes are proposed to siphon CoA from primary metabolism to create the side chains for the pre

157 remains one of the least understood areas of primary metabolism to date.

158 rve as ideal hosts and how to optimize plant primary metabolism to efficiently provide precursors for

159 e and oxidative pentose-phosphate pathway in primary metabolism to phenylpropanoid biosynthesis by co

160 r, little is known about the contribution of primary metabolism to the evolution of specialized metab

161 diverts the central flux of carbon from the primary metabolism to the synthesis of myriad phenolics.

162 ; it diverts the central flux of carbon from primary metabolism to the synthesis of myriad phenolics.

163 A substantial proportion of primary metabolism transcripts were decreased in border

164 plant, leaf, and cellular level showed that primary metabolism was reduced by growth in limiting N,

165 omata suggests a significant manipulation of primary metabolism, we also characterized the gall trans

166 onserved and evolutionarily ancient genes of primary metabolism were activated at intermediate time p

167 d activities of the main enzymes involved in primary metabolism were compared.

168 Major pathways in primary metabolism were identified, indicating significa

169 quires JA-Ile signaling-dependent changes in primary metabolism, which are not compromised in the COI

170 d expressed sequence tags several enzymes of primary metabolism whose expression during spore germina

171 biosynthesis is an important link connecting primary metabolism with development.

172 this pathway is an important link connecting primary metabolism with development.