ライフサイエンスコーパス: aminocyclopropane

1 further synthetic transformations affording aminocyclopropanes.

2 a highly practical preparation of protected aminocyclopropanes.

3 plants treated with the ethylene precursor 1-aminocyclopropane- 1-carboxylic acid and by examination

4 d, salicylic acid), chemicals (clofibrate, 1-aminocyclopropane-1 carboxylic acid), or environmental s

5 qEL7 encodes 1-aminocyclopropane-1- carboxylate oxidase2 (ACO2), a gene

6 a-chloro-L-aminobutyryl-S-CmaD, generating 1-aminocyclopropane-1-carbonyl (ACC)-S-CmaD.

7 that induce ethylene biosynthesis, such as 1-aminocyclopropane-1-carboxylate (ACC) and auxin, also en

8 uting and regulated gibberellins (GA(3)) and aminocyclopropane-1-carboxylate (ACC) content along with

9 1-Aminocyclopropane-1-carboxylate (ACC) deaminase is a pyr

10 1-aminocyclopropane-1-carboxylate (ACC) deaminase is a pyr

11 nt growth.Bacteria that produce the enzyme 1-aminocyclopropane-1-carboxylate (ACC) deaminase, when pr

12 versible inhibitor for a bacterial enzyme, 1-aminocyclopropane-1-carboxylate (ACC) deaminase, which c

13 n of DGD-K+ with the competitive inhibitor 1-aminocyclopropane-1-carboxylate (ACC) lowers both kcat a

14 1-Aminocyclopropane-1-carboxylate (ACC) oxidase catalyzes

15 for the expression in Escherichia coli of 1-aminocyclopropane-1-carboxylate (ACC) oxidase from kiwi

16 imiting enzyme of ethylene biosynthesis is 1-aminocyclopropane-1-carboxylate (ACC) synthase (ACS), wh

17 Inhibition of ethylene biosynthesis genes, 1-aminocyclopropane-1-carboxylate (ACC) synthase and ACC o

18 idoxal phosphate- (PLP-) dependent enzymes 1-aminocyclopropane-1-carboxylate (ACC) synthase and aspar

19 shown to be a mechanism-based inhibitor of 1-aminocyclopropane-1-carboxylate (ACC) synthase as well a

20 1-Aminocyclopropane-1-carboxylate (ACC) synthase catalyzes

21 estigated the expression patterns of three 1-aminocyclopropane-1-carboxylate (ACC) synthase genes in

22 l and spatial expression patterns of three 1-aminocyclopropane-1-carboxylate (ACC) synthase genes wer

23 gs by rapidly increasing the expression of 1-aminocyclopropane-1-carboxylate (ACC) synthase mRNA and

24 1-Aminocyclopropane-1-carboxylate (ACC) synthase, a member

25 he transcript levels of two genes encoding 1-aminocyclopropane-1-carboxylate (ACC) synthase, Ps-ACS1

26 sequences of genes encoding homologues of 1-aminocyclopropane-1-carboxylate (ACC) synthase, the firs

27 Two catalytically inactive mutant forms of 1-aminocyclopropane-1-carboxylate (ACC) synthase, Y85A and

28 d organs, but also enhance the activity of 1-aminocyclopropane-1-carboxylate (ACC) synthase.

29 The screen also identified 1-AMINOCYCLOPROPANE-1-CARBOXYLATE (ACC) SYNTHASE7, an ACC

30 Glutamate 47 is conserved in 1-aminocyclopropane-1-carboxylate (ACC) synthases and is p

31 the effects of ethylene by application of 1-aminocyclopropane-1-carboxylate (ACC) to paradormant pla

32 ia degradation of its immediate precursor, 1-aminocyclopropane-1-carboxylate (ACC), in the rhizospher

33 actate or the covalently binding inhibitor 1-aminocyclopropane-1-carboxylate all induce a slow change

34 mixing time of these measurements for both 1-aminocyclopropane-1-carboxylate and 2-methyl-2-aminomalo

35 r PGPR traits, including P solubilization, 1-aminocyclopropane-1-carboxylate deaminase activity, and

36 ied the role of ethylene and its precursor 1-aminocyclopropane-1-carboxylate in several biological pr

37 1-Aminocyclopropane-1-carboxylate oxidase (ACC oxidase) ca

38 lopropane-1-carboxylate synthase (ACS) and 1-aminocyclopropane-1-carboxylate oxidase (ACO).

39 a fragment of a petunia gene encoding for 1-aminocyclopropane-1-carboxylate oxidase (ACO4) Abundance

40 RPW8.1 binds and stabilizes 1-aminocyclopropane-1-carboxylate oxidase 4 (ACO4), which

41 finger CCCH protein, glycosyltransferase, 1-aminocyclopropane-1-carboxylate oxidase homologs, recept

42 1-Aminocyclopropane-1-carboxylate synthase (ACC synthase,

43 enase 7 (lox7), lipoxygenase 8 (lox8), and 1-aminocyclopropane-1-carboxylate synthase (acc-s)].

44 criptional regulations of its key enzymes, 1-aminocyclopropane-1-carboxylate synthase (ACS) and 1-ami

45 1-Aminocyclopropane-1-carboxylate synthase (ACS) catalyzes

46 The structures of tomato 1-aminocyclopropane-1-carboxylate synthase (ACS) in comple

47 In Arabidopsis thaliana, 1-aminocyclopropane-1-carboxylate synthase (ACS) is encode

48 In most plant species, 1-aminocyclopropane-1-carboxylate synthase (ACS) is the ke

49 hat 14-3-3 proteins interact with multiple 1-aminocyclopropane-1-carboxylate synthase (ACS) isoforms

50 o-step biosynthetic pathway of ethylene is 1-aminocyclopropane-1-carboxylate synthase (ACS), which ca

51 The pyridoxal phosphate-dependent enzyme 1-aminocyclopropane-1-carboxylate synthase (ACS, EC 4.4.1.

52 The pyridoxal phosphate-dependent enzyme, 1-aminocyclopropane-1-carboxylate synthase (ACS; EC 4.4.1.

53 d via ethylene signaling,(3) expression of 1-AMINOCYCLOPROPANE-1-CARBOXYLATE SYNTHASE 7 (ACS7) is inc

54 y conserved, where the only exceptions are 1-aminocyclopropane-1-carboxylate synthase and CobD.

55 f the Arabidopsis gene family that encodes 1-aminocyclopropane-1-carboxylate synthase, the first enzy

56 rs of two key ethylene biosynthesis genes (1-aminocyclopropane-1-carboxylate synthase: SlACS2 and SlA

57 DCA storage reduces ACC (1-aminocyclopropane-1-carboxylate) oxidase activity, ethyl

58 Similar to calcium, SA, 1-aminocyclopropane-1-carboxylic acid (a precursor to ethy

59 ellin peptide (flg22) and the ET precursor 1-aminocyclopropane-1-carboxylic acid (ACC) but is blocked

60 The ethylene precursor 1-aminocyclopropane-1-carboxylic acid (ACC) conjugated to

61 Indole-3-acetic acid (IAA) and 1-aminocyclopropane-1-carboxylic acid (ACC) differentially

62 In seed plants, 1-aminocyclopropane-1-carboxylic acid (ACC) is the precurs

63 We show that repression by 1-aminocyclopropane-1-carboxylic acid (ACC) of the Glc-dep

64 f transgenic seedlings treated with either 1-aminocyclopropane-1-carboxylic acid (ACC) or alpha-napht

65 hesis in plants is catalyzed by the enzyme 1-aminocyclopropane-1-carboxylic acid (ACC) oxidase (ACCO)

66 1-Aminocyclopropane-1-carboxylic acid (ACC) oxidase (ACCO)

67 1-Aminocyclopropane-1-carboxylic acid (ACC) oxidase (ACCO)

68 production correlated with an increase in 1-aminocyclopropane-1-carboxylic acid (ACC) oxidase (ACO)

69 ts show that the mutant's abundance of the 1-aminocyclopropane-1-carboxylic acid (ACC) oxidase mRNA S

70 Wounding increased 1-aminocyclopropane-1-carboxylic acid (ACC) oxidase protei

71 t ripening and senescence, is catalyzed by 1-aminocyclopropane-1-carboxylic acid (ACC) oxidase.

72 type, etiolated seedlings through distinct 1-aminocyclopropane-1-carboxylic acid (ACC) synthase (ACS)

73 SIPK coincided with a dramatic increase in 1-aminocyclopropane-1-carboxylic acid (ACC) synthase (ACS)

74 Two partial 1-aminocyclopropane-1-carboxylic acid (ACC) synthase cDNA

75 ver, expression analysis on members of the 1-aminocyclopropane-1-carboxylic acid (ACC) synthase ethyl

76 ppressed by the expression of an antisense 1-aminocyclopropane-1-carboxylic acid (ACC) synthase gene

77 erized an Arabidopsis cDNA (ACS6) encoding 1-aminocyclopropane-1-carboxylic acid (ACC) synthase which

78 fei2 roots was suppressed by inhibition of 1-aminocyclopropane-1-carboxylic acid (ACC) synthase, an e

79 methyladenosine (m(6)A) reader, and ACS2, an aminocyclopropane-1-carboxylic acid (ACC) synthase, whic

80 , VpMAPK6, VpACS1 and VpACS2 in vivo (ACS, 1-aminocyclopropane-1-carboxylic acid (ACC) synthase; MAPK

81 A key target of this regulation is 1-aminocyclopropane-1-carboxylic acid (ACC) synthases (ACS

82 We demonstrate that as a scaffold, 1-aminocyclopropane-1-carboxylic acid (ACC) synthases (ACS

83 ne biosynthesis is directed by a family of 1-aminocyclopropane-1-carboxylic acid (ACC) synthases (ACS

84 on via the light-mediated stabilization of 1-aminocyclopropane-1-carboxylic acid (ACC) synthases (ACS

85 the application of the ethylene precursor 1-aminocyclopropane-1-carboxylic acid (ACC) to pollinated

86 tep in ethylene biosynthesis, oxidation of 1-aminocyclopropane-1-carboxylic acid (ACC) to yield ethyl

87 nous application of the ethylene precursor 1-aminocyclopropane-1-carboxylic acid (ACC) was found to p

88 as treatments with salicylic acid (SA) and 1-aminocyclopropane-1-carboxylic acid (ACC) were ineffecti

89 hree cyclic and three acyclic analogues of 1-aminocyclopropane-1-carboxylic acid (ACC) with ACC oxida

90 and coronamic acid (CMA), which resembles 1-aminocyclopropane-1-carboxylic acid (ACC), a precursor t

91 treatment of plants with the ET precursor 1-aminocyclopropane-1-carboxylic acid (ACC), activation of

92 1-aminocyclopropane-1-carboxylic acid (ACC), benzyladenine

93 Its immediate precursor, 1-aminocyclopropane-1-carboxylic acid (ACC), is a non-prot

94 1 mutations, or through the application of 1-aminocyclopropane-1-carboxylic acid (ACC), negatively im

95 w concentrations of the ethylene precursor 1-aminocyclopropane-1-carboxylic acid (ACC), promotes the

96 ntly increased the content of free Met and 1-aminocyclopropane-1-carboxylic acid (ACC), the immediate

97 -inducing hormone ethylene, or its precursor aminocyclopropane-1-carboxylic acid (ACC), to the flower

98 The roots of flooded plants produce 1-aminocyclopropane-1-carboxylic acid (ACC), which is tran

99 wing treatment with the ethylene precursor 1-aminocyclopropane-1-carboxylic acid (ACC).

100 es that convert S-adenosyl-L-methionine to 1-aminocyclopropane-1-carboxylic acid (ACC)] and PsACO (en

101 hypocotyl under -DIF was restored by both 1-aminocyclopropane-1-carboxylic acid (ACC; ethylene precu

102 phic and electrophysiological studies with 1-aminocyclopropane-1-carboxylic acid (ACPC), 1-aminocyclo

103 een the previously observed stress-induced 1-aminocyclopropane-1-carboxylic acid accumulation and DEL

104 1-Aminocyclopropane-1-carboxylic acid and 2,4-dichlorophen

105 e ribosomal protein L29 and presequence of 1-aminocyclopropane-1-carboxylic acid deaminase 1) and N-

106 genotypes impaired in ethylene synthesis (1-aminocyclopropane-1-carboxylic acid deaminase) and perce

107 the pyridoxal 5'-phosphate (PLP)-dependent 1-aminocyclopropane-1-carboxylic acid deaminases.

108 Applied 1-aminocyclopropane-1-carboxylic acid increased adventitio

109 o knock out the five ethylene-biosynthesis 1-aminocyclopropane-1-carboxylic acid oxidase (ACO) genes

110 n plant cells, suppressing the activity of 1-aminocyclopropane-1-carboxylic acid oxidase (ACO), the e

111 olution of plant-derived nonheme Fe enzyme 1-aminocyclopropane-1-carboxylic acid oxidase into a nitro

112 nd our previously evolved ACCO(Nim) (ACCO: 1-aminocyclopropane-1-carboxylic acid oxidase) exhibited c

113 propane-1-carboxylic acid, as catalyzed by 1-aminocyclopropane-1-carboxylic acid oxidase.

114 ne production is shut down at the level of 1-aminocyclopropane-1-carboxylic acid oxidase.

115 chanisms for Cellulose synthase (CesA) and 1-Aminocyclopropane-1-carboxylic acid oxidase1 and 3 (ACO1

116 plants treated with the ethylene precursor 1-aminocyclopropane-1-carboxylic acid showed a root-specif

117 1-Aminocyclopropane-1-carboxylic acid synthase (ACS) is th

118 ermore, we found that selected isoforms of 1-aminocyclopropane-1-carboxylic acid synthase (ACS), the

119 S9, respectively; these encode isozymes of 1-aminocyclopropane-1-carboxylic acid synthase (ACS), whic

120 ect the post-transcriptional regulation of 1-aminocyclopropane-1-carboxylic acid synthase (ACS).

121 At the same time, 1-aminocyclopropane-1-carboxylic acid synthase activity in

122 plant showed only a moderate regulation of 1-aminocyclopropane-1-carboxylic acid synthase and Yang cy

123 ed by sequence alignment of genes encoding 1-aminocyclopropane-1-carboxylic acid synthase from both a

124 crease ethylene production and expression of aminocyclopropane-1-carboxylic acid synthase gene, the f

125 ted the auxin induction of only one of two 1-aminocyclopropane-1-carboxylic acid synthase genes that

126 Expression of members of the LeACS (1-aminocyclopropane-1-carboxylic acid synthase, a key regu

127 be mediated by increase in net activity of 1-aminocyclopropane-1-carboxylic acid synthase, it might r

128 e production by increasing the activity of 1-aminocyclopropane-1-carboxylic acid synthase.

129 orm accelerated transformation of vacuolar 1-aminocyclopropane-1-carboxylic acid to ethylene.

130 racterized, with one corresponding to ACC (1-aminocyclopropane-1-carboxylic acid) oxidase, three to p

131 omules were induced by treatment with ACC (1-aminocyclopropane-1-carboxylic acid), the first committe

132 eous treatment with an ethylene precursor (1-aminocyclopropane-1-carboxylic acid).

133 IAA), axr1-24 had decreased sensitivity to 1-aminocyclopropane-1-carboxylic acid, 6-benzylamino-purin

134 ibition can be reversed by the addition of 1-aminocyclopropane-1-carboxylic acid, a direct precursor

135 ignaling pathways, whereas the addition of 1-aminocyclopropane-1-carboxylic acid, a direct precursor

136 st-veraison with a clear ethylene precursor (aminocyclopropane-1-carboxylic acid, ACC) peak before ve

137 ants, ethylene is produced by oxidation of 1-aminocyclopropane-1-carboxylic acid, as catalyzed by 1-a

138 ses when treated with ethylene rather than 1-aminocyclopropane-1-carboxylic acid, but had increased l

139 uxin, cytokinin, or the ethylene precursor 1-aminocyclopropane-1-carboxylic acid, indicating that the

140 of ethylene precursors, S-adenosyl-Met and 1-aminocyclopropane-1-carboxylic acid, or PA biosynthesis

141 ibitor II gene in response to Botrytis and 1-aminocyclopropane-1-carboxylic acid, the natural precurs

142 BAP increases ABA levels in the shoot and 1-aminocyclopropane-1-carboxylic acid, the rate-limiting p

143 e, L-Trp, L-Ala, or the ethylene precursor 1-aminocyclopropane-1-carboxylic acid.

144 ty to exogenous ethylene and its precursor 1-aminocyclopropane-1-carboxylic acid.

145 complex with substrate ACC, an inhibitor, 1-aminocyclopropane-1-phosphonate (ACP), the product alpha

146 dologies are highlighted, and examples where aminocyclopropanes are exploited as key intermediates in

147 nantioenriched beta-hydroxy (E)-enamines and aminocyclopropanes are presented.

148 Aminocyclopropanes are versatile building blocks for acc

149 avage of the methyl carbamate gives the free aminocyclopropanes as their HI salts.

150 on of Rh and CO into one of the two proximal aminocyclopropane C-C bonds.

151 n the catalyst (at the i+2 position) from an aminocyclopropane carboxamide residue (97:3 er) to an am

152 results in the oxidative ring cleavage of 1-aminocyclopropane carboxylate (ACC) into ethylene, cyani

153 and ACS (a possible homologue of the plant 1-aminocyclopropane-carboxylate synthase gene).

154 Imines, obtained via simple condensation of aminocyclopropane carboxylates (ACPC) with a broad range

155 mbia seedlings with the ethylene precursor 1-aminocyclopropane carboxylic acid (ACC) reduced root elo

156 , or treatment with the ethylene precursor 1-aminocyclopropane carboxylic acid (ACC), reduces lateral

157 same sensitivity to the ethylene precursor 1-aminocyclopropane carboxylic acid as wild-type plants, a

158 d by treatment with the ethylene precursor 1-aminocyclopropane carboxylic acid in etiolated hypocotyl

159 jasmonate (MeJA), and the ethylene precursor aminocyclopropane carboxylic acid.

160 te agonists were glycine, D-cycloserine, and aminocyclopropane-carboxylic acid.

161 especially auxin and the ethylene precursor aminocyclopropane-carboxylic acid.

162 Aminocyclopropanes equipped with pendant nucleophiles un

163 Aminocyclopropanes equipped with suitable N-directing gr

164 ferent elicitors (sucrose, mannitol, NaCl, 1-aminocyclopropane-L-carboxylic acid, salicylic acid and

165 ve been developed for the preparation of the aminocyclopropane moiety (Kulinkovich reactions applied

166 ane synthase (ZmAcs2, ZmAcs6, and ZmAcs7), 1-aminocyclopropane oxidase (Aco15, Aco20, Aco31, and Aco3

167 The review encompasses cases where aminocyclopropanes participate in polar reactions, peric

168 ncrease in the expression level of several 1-aminocyclopropane synthase (ZmAcs2, ZmAcs6, and ZmAcs7),

169 progress in ring-opening transformations of aminocyclopropanes via radical intermediates, divided in

170 ic asymmetric [3 + 2] annulation reaction of aminocyclopropanes with both enol ethers and aldehydes.