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1 or assimilation of acetate in the absence of isocitrate lyase.
2 se with only an NAD-dependent IDH never have isocitrate lyase.
3 t this enzyme is regulated differentially to isocitrate lyase.
4  inhibited import of the peroxisomal protein isocitrate lyase.
5 as imported more efficiently than oligomeric isocitrate lyase.
6 eA) which exhibits a low similarity to other isocitrate lyases.
7 ose-1,6-bisphosphatase 1) and ICL1 (encoding isocitrate lyase 1) are under control of the Mig1 repres
8 sis thaliana to identify the segments of the isocitrate lyase 5' flanking region that influence promo
9                                              Isocitrate lyase, a glyoxysomal protein, and the leaf-ty
10                                  Activity of isocitrate lyase AceA, an S-allylmercapto-modified candi
11                               Genes encoding isocitrate lyase (aceA) and malate synthase (aceB), both
12 re linked through enzymatic redundancy, with isocitrate lyase (AceA) exhibiting secondary 2-methyliso
13                                           An isocitrate lyase (aceA) mutant was virulent, so the inab
14                                              Isocitrate lyase (AceA) was induced by oxygen across the
15                                   A putative isocitrate lyase (aceA; blr2455) was among the most stro
16 eling is mediated by the bifunctional enzyme isocitrate lyase acting in a noncanonical role distinct
17 l-coenzyme A synthetase; Acs) expression and isocitrate lyase activity without affecting key TCA cycl
18 as AceA proteins, and show that both exhibit isocitrate lyase activity.
19 cleotide sequence of the structural gene for isocitrate lyase (acu-7) is presented and features of it
20 d comparison with the closed conformation of isocitrate lyase and 2-methylisocitrate lyase revealed t
21 ssion of the latent infection genes encoding isocitrate lyase and alpha-crystallin, respectively.
22 st serine cycle methylotrophic bacteria lack isocitrate lyase and convert acetyl coenzyme A (acetyl-C
23 ass of the tricarboxylic acid cycle in which isocitrate lyase and malate synthase (GlcB) catalyze the
24                                 In addition, isocitrate lyase and malate synthase activities were six
25      Enzyme assays validated the increase in isocitrate lyase and malate synthase activities.
26             In this study the genes encoding isocitrate lyase and malate synthase from Chlorogloeopsi
27 showed strong homology to gene sequences for isocitrate lyase and malate synthase from plants and oth
28                    Transcript abundances for isocitrate lyase and malate synthase increased, and C. f
29                      When the genes encoding isocitrate lyase and malate synthase were expressed in S
30 ve expression of the glyoxylate shunt genes (isocitrate lyase and malate synthase) was >300-fold high
31 n for the two glyoxylate cycle (GC) enzymes, isocitrate lyase and malate synthase, are expressed in a
32  Previous studies reported the activities of isocitrate lyase and malate synthase, the key enzymes of
33 ural rearrangement, substantially increasing isocitrate lyase and methylisocitrate lyase activities.
34 In order to specifically address the role of isocitrate lyase and nitrogenase in chemoautotrophic gro
35 w that two additional gluconeogenic enzymes, isocitrate lyase and phosphoenolpyruvate carboxykinase,
36 ed for two other enzyme superfamily members, isocitrate lyase and phosphoenolpyruvate mutase.
37 sphosphatase (FBPase), malate dehydrogenase, isocitrate lyase, and phosphoenolpyruvate carboxykinase
38 tress-related alkyl hydroperoxide reductase, isocitrate lyase, and the cell surface protein A.
39         mRNA for the glyoxylate cycle enzyme isocitrate lyase declined at similar rates in patients r
40                                           An isocitrate lyase-deficient mutant of Mtb (Deltaicl1) exh
41 nt in glyoxylate shunt enzymes, specifically isocitrate lyase (DeltaaceA) and malate synthase (Deltaa
42                                              Isocitrate lyase-dependent production of succinate affor
43 ne the chemical function a new member of the isocitrate lyase enzyme family derived from the flowerin
44 osely related phosphoenolpyruvate mutase and isocitrate lyase enzymes.
45 on of elements is involved in regulating the isocitrate lyase gene and that distinct DNA sequences pl
46  with PR genes and highest expression of the isocitrate lyase gene coinciding with highest solar irra
47 sequences that regulate the expression of an isocitrate lyase gene from Brassica napus L. during late
48                    We showed previously that isocitrate lyase (ICL) activity is constitutively upregu
49 CoA (HS-CoA) and, on the other hand, between isocitrate lyase (ICL) and isocitrate dehydrogenase (ICD
50 sition in which the glyoxylate cycle enzymes isocitrate lyase (ICL) and malate synthase (MLS) are rep
51 cised and incubated without a carbon source, isocitrate lyase (ICL) and malate synthase (MS) mRNAs in
52 like isoforms of the glyoxylate cycle enzyme isocitrate lyase (ICL) are jointly required for fatty ac
53 uch information is, however, lacking for the isocitrate lyase (Icl) gene which is coordinately regula
54           A cDNA with sequence similarity to isocitrate lyase (ICL) genes was isolated from the unice
55                                  The role of isocitrate lyase (ICL) in the glyoxylate cycle and its n
56                                              Isocitrate lyase (ICL) is a peroxisomal glyoxylate cycle
57  The activity of the glyoxylate cycle enzyme isocitrate lyase (ICL) was surveyed in eight barley cult
58 of M. tuberculosis in mice is facilitated by isocitrate lyase (ICL), an enzyme essential for the meta
59 at the first enzyme of the glyoxylate shunt, isocitrate lyase (ICL), may mediate survival of Mtb duri
60             In addition to the inhibition of isocitrate lyase (ICL), we demonstrate that itaconate in
61 nd C2 compounds in an unknown pathway in the isocitrate lyase (ICL)-negative Methylobacterium.
62  glyoxysomal/peroxisomal targeting signal of isocitrate lyase (ICL).
63  pseudotuberculosis, constitutively produces isocitrate lyase (ICL).
64                                              Isocitrate lyase (ICL, types 1 and 2) is the first enzym
65 e principal enzymes of the glyoxylate cycle, isocitrate lyase (ICL1) and malate synthase (MLS1).
66 this profiling, a single gene for the enzyme isocitrate lyase (ICL1) was found to be up regulated at
67 A]], homodomain transcription factor [StlA], isocitrate lyase [Icl1], polyaromatic amino acid biosynt
68    Although MCLs share limited homology with isocitrate lyases (ICLs) of the glyoxylate cycle, these
69  all three drugs trigger activation of Mtb's isocitrate lyases (ICLs), metabolic enzymes commonly ass
70 s (Mtb) more profoundly than deletion of its isocitrate lyases (ICLs).
71                                              Isocitrate lyase (IL) is an essential enzyme in the glyo
72                                              Isocitrate lyase is a key enzyme in the glyoxylate cycle
73 s in fungi, in conjunction with reports that isocitrate lyase is both upregulated and required for th
74 erculosis the production and activity of the isocitrate lyase is enhanced under minimal growth condit
75                                     Although isocitrate lyase is essential for Salmonella persistence
76                                              Isocitrate lyase is important for lipid utilisation by M
77                                              Isocitrate lyase is required for fatty acid utilization
78                                              Isocitrate lyase is stabilized in pex4 pex22, indicating
79 In contrast, ABA repressed the expression of isocitrate lyase (ll9) mRNA.
80 s in central carbon metabolism, specifically isocitrate lyase, malate synthase, transaldolase, fructo
81                                              Isocitrate lyase mRNA correlated highly with CFU in sput
82                            Data suggest that isocitrate lyase mRNA is a reliable marker of M. tubercu
83                                              Isocitrate lyase mRNA was detectable in sputum of cultur
84 abase (Sanger) with similarity to the enzyme isocitrate lyase of both Corynebacterium glutamicum and
85 three enzymes are: trace levels of OGDH, the isocitrate lyase of the glyoxylate shunt and an unantici
86 ame shows significant sequence similarity to isocitrate lyases of bacteria (70%), molds (48%), yeasts
87 ngus Magnaporthe grisea, a gene that encodes isocitrate lyase, one of the principal enzymes of the gl
88 n feed into either the glyoxylate shunt (via isocitrate lyase) or the TCA cycle (via isocitrate dehyd
89 ranscriptional regulators and genes encoding isocitrate lyase, oxidative stress responses, the synthe
90                                          The isocitrate lyase paralogs of Mycobacterium tuberculosis
91 , Shewanella oneidensis MR-1 uses the serine-isocitrate lyase pathway common to many methylotrophic a
92             To examine its use of the serine-isocitrate lyase pathway under anaerobic conditions, we
93 rel fold of PDP is the same as that of other isocitrate lyase/PEP mutase superfamily members, includi
94 mber of the phosphoenolpyruvate (PEP) mutase/isocitrate lyase (PEPM/ICL) superfamily, hydrolyzes P-py
95 ted enzymes-such as glutamine synthetase and isocitrate lyase-perform redox neutral chemical transfor
96 markers common to the C-C bond lyases of the isocitrate lyase/phosphoenolpyruvate mutase superfamily,
97  and sigH (alternative sigma factors), aceA (isocitrate lyase), ponA (class I penicillin-binding prot
98  of the PRC2-repressed glyoxylate cycle gene ISOCITRATE LYASE promotes the vegetative phase transitio
99 he proposed mechanism of the closely related isocitrate lyases, PrpB residue C123 is proposed to serv
100 ns, although glyoxylate synthesized from the isocitrate lyase reaction can be converted to glycine, a
101 d inhibits the growth of bacteria expressing isocitrate lyase, such as Salmonella enterica and Mycoba
102 at they lack the key glyoxylate cycle enzyme isocitrate lyase, suggesting that alternative pathway(s)
103  functionally novel member of the PEP mutase/isocitrate lyase superfamily and therefore targeted for
104                     As with other PEP mutase/isocitrate lyase superfamily members, the protein assemb
105 ase branch of the phosphoenolpyruvate mutase/isocitrate lyase superfamily to provide insight into the
106 , a member of the phosphoenolpyruvate mutase/isocitrate lyase superfamily, catalyzes the hydrolysis o
107 at belongs to the phosphoenolpyruvate mutase/isocitrate lyase superfamily.
108  two unique enzymes of the glyoxylate cycle, isocitrate lyase (TaICL) and malate synthase, diverged i
109 Methylobacterium extorquens AM1, which lacks isocitrate lyase, the key enzyme in the glyoxylate cycle
110 ic acid is an organic compound that inhibits isocitrate lyase, the key enzyme of the glyoxylate shunt
111 tumefaciens BlcR is a member of the emerging isocitrate lyase transcription regulators that negativel
112 ack of phosphoenolpyruvate carboxykinase and isocitrate lyase, two enzymes necessary for lipid assimi
113 structure of the targeted protein; monomeric isocitrate lyase was imported more efficiently than olig
114     Mutants of the glyoxylate shunt gene for isocitrate lyase were able to grow in the presence of oi
115                 Various known inhibitors for isocitrate lyase were effective.
116 nomes reveals that those genomes that encode isocitrate lyase, which is essential for growth on aceta

 
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