ライフサイエンスコーパス: fatty acid biosynthesis

1 f acetyl-CoA carboxylase and polyunsaturated fatty acid biosynthesis.

2 , from the TCA cycle for use in HCMV-induced fatty acid biosynthesis.

3 tion of the malonyl-CoA precursor of de novo fatty acid biosynthesis.

4 d gluconeogenesis but funneled directly into fatty acid biosynthesis.

5 cation: autophagy, actin polymerization, and fatty acid biosynthesis.

6 an oxygen consuming, rate-limiting enzyme in fatty acid biosynthesis.

7 which catalyzes the first enzymatic step of fatty acid biosynthesis.

8 etoxifying reactive carbonyls and regulating fatty acid biosynthesis.

9 biosynthesis and 5 genes specify aspects of fatty acid biosynthesis.

10 ylCoA carboxylase (ACC), the first enzyme in fatty acid biosynthesis.

11 yses the first committed step in prokaryotic fatty acid biosynthesis.

12 r enzymes at the first major branch point in fatty acid biosynthesis.

13 antibacterial activity through inhibition of fatty acid biosynthesis.

14 AtpC, RpoA, and several proteins involved in fatty acid biosynthesis.

15 pathways: glycerophospholipid metabolism and fatty acid biosynthesis.

16 g the chain-elongation reaction of bacterial fatty acid biosynthesis.

17 oth of which are involved in cholesterol and fatty acid biosynthesis.

18 (also known as BCCP), which is required for fatty acid biosynthesis.

19 me that catalyzes the last reductive step of fatty acid biosynthesis.

20 st reductive step in the elongation cycle of fatty acid biosynthesis.

21 PDC provides acetyl-CoA and NADH for de novo fatty acid biosynthesis.

22 noyl reductase enzyme from type II bacterial fatty acid biosynthesis.

23 esis and the less well exploited pathway for fatty acid biosynthesis.

24 ondensing enzyme that plays central roles in fatty acid biosynthesis.

25 w antibacterial compounds are the enzymes of fatty acid biosynthesis.

26 otein that is an essential cofactor in plant fatty acid biosynthesis.

27 yzes the first committed reaction of de novo fatty acid biosynthesis.

28 ntify a potential regulatory role of ACPS in fatty acid biosynthesis.

29 P) is then active as the central coenzyme of fatty acid biosynthesis.

30 biosynthetic process that closely parallels fatty acid biosynthesis.

31 te genes encoding enzymes of cholesterol and fatty acid biosynthesis.

32 ACP) synthase III (FabH or KS III) enzyme of fatty acid biosynthesis.

33 where they activate genes of cholesterol and fatty acid biosynthesis.

34 CoA from acetyl CoA, a rate-limiting step in fatty acid biosynthesis.

35 y participate in determining the products of fatty acid biosynthesis.

36 ltienzyme complex involved in branched-chain fatty acid biosynthesis.

37 tion of genes encoding enzymes of sterol and fatty acid biosynthesis.

38 e that catalyzes the first committed step of fatty acid biosynthesis.

39 lesterol biosynthesis, the LDL receptor, and fatty acid biosynthesis.

40 ffect of 25-hydroxycholesterol on sterol and fatty acid biosynthesis.

41 atty acid degradation and as an activator of fatty acid biosynthesis.

42 that BPL-1 is required for efficient de novo fatty acid biosynthesis.

43 (ACP) with acetyl-CoA in plant and bacterial fatty acid biosynthesis.

44 ulation of fatty acid oxidation, rather than fatty acid biosynthesis.

45 ters for key enzymes of both cholesterol and fatty acid biosynthesis.

46 ier protein) (holo-ACPP) in an early step of fatty acid biosynthesis.

47 hat controls the first rate-limiting step in fatty acid biosynthesis.

48 scription factors regulating cholesterol and fatty acid biosynthesis.

49 ase) catalyzes the committed step of de novo fatty acid biosynthesis.

50 th exogenous fatty acids and de novo type II fatty acid biosynthesis.

51 directly confer sensitivity to inhibitors of fatty acid biosynthesis.

52 and may also require increasing the flux of fatty acid biosynthesis.

53 ion relevant to understanding polyketide and fatty acid biosynthesis.

54 e the multidomain protein can participate in fatty acid biosynthesis.

55 correlated with a decrease in branched-chain fatty acid biosynthesis.

56 ricarboxylic acid metabolism (TCA) cycle and fatty acid biosynthesis.

57 tions in either amino acid concentrations or fatty acid biosynthesis.

58 acetyl-CoA to the cytosol for the essential fatty acid biosynthesis.

59 ete down-regulation of proteins required for fatty acid biosynthesis.

60 reconstituted in vitro by coupling Gcs with fatty acid biosynthesis.

61 ds of the Arabidopsis (Arabidopsis thaliana) fatty acid biosynthesis 1 (fab1) mutant contain a 35% to

62 ression of several hepatic genes involved in fatty acid biosynthesis, 2) elevated postprandial fatty

63 Importantly, the rate-limiting enzyme of fatty acid biosynthesis, acetyl-CoA carboxylase 1 (ACC1)

64 ed in lignan synthesis, cell elongation, and fatty acid biosynthesis, all of which have important rol

65 Bacterial genes involved in fatty acid biosynthesis, amounts of lactobacilli, and sa

66 production, including 9% to 19% of carbon to fatty acid biosynthesis and 32% to 46% of carbon to amin

67 sing enzymes, is a key catalyst in bacterial fatty acid biosynthesis and a promising target for novel

68 of the acyl carrier protein (ACP) as used in fatty acid biosynthesis and a range of other metabolic e

69 -2 processing and prevented the induction of fatty acid biosynthesis and ACC1 expression.

70 mellitus in animals leads to a reduction of fatty acid biosynthesis and an upregulation of an altern

71 ell as in providing a tool for investigating fatty acid biosynthesis and catabolism.

72 ee interconnected pathways (innate immunity, fatty acid biosynthesis and cholesterol biosynthesis) in

73 ion factor FadR regulates genes required for fatty acid biosynthesis and degradation in an opposing m

74 rward loop regulating the transition between fatty acid biosynthesis and degradation in V. cholerae O

75 air C. elegans fertility identified genes in fatty acid biosynthesis and ethanolamine utilization pat

76 y relevant drug target, we demonstrated that fatty acid biosynthesis and FabI activity are essential

77 g an intermediate in the pathways of de novo fatty acid biosynthesis and fatty acid elongation, malon

78 well as other associated pathways including fatty acid biosynthesis and glycolysis.

79 for essential biosynthetic processes such as fatty acid biosynthesis and haem biosynthesis, the two l

80 a transporter genes that are associated with fatty acid biosynthesis and intracellular lipid traffick

81 e for catalyzing the final step of bacterial fatty acid biosynthesis and is an attractive target for

82 es the final step in each cycle of bacterial fatty acid biosynthesis and is an attractive target for

83 et, since it is central to the initiation of fatty acid biosynthesis and is highly conserved among Gr

84 ein reductase (ENR) is involved in bacterial fatty acid biosynthesis and is the target of the antibac

85 The primary ones are type II fatty acid biosynthesis and isoprenoid biosynthesis.

86 C1), an enzyme with crucial roles in de novo fatty acid biosynthesis and lipogenesis and essential fo

87 t, revealing a feedback loop between omega-9 fatty acid biosynthesis and MSI1 activity.

88 ostatic cancers exhibit increased endogenous fatty acid biosynthesis and overexpress certain enzymes

89 and malonyl-CoA levels, thereby influencing fatty acid biosynthesis and oxidation.

90 inate the acyl-acyl carrier protein track of fatty acid biosynthesis and play an essential role in de

91 The fatty acyl group is derived from fatty acid biosynthesis and provides signal specificity,

92 ter, this suggests a functional link between fatty acid biosynthesis and R1128 biosynthesis in the en

93 FMT and had increased levels of short-chain fatty acid biosynthesis and secondary bile acids.

94 modulated energy homeostasis by suppressing fatty acid biosynthesis and shifting the metabolism to o

95 ogy of ARM, including pathways involved with fatty acid biosynthesis and the complement system.

96 ivity, avoiding the detrimental reduction in fatty acid biosynthesis and the concomitant detrimental

97 ATP(lo)pyruvate(lo) conditions triggered fatty acid biosynthesis and the formation of cytoplasmic

98 at least two genes required for unsaturated fatty acid biosynthesis and the gene encoding the transc

99 Both the activation of fatty acid biosynthesis and the sensitivity to fatty aci

100 of genes encoding enzymes of cholesterol and fatty acid biosynthesis and uptake.

101 ion of WRINKLED1, a key regulator of plastid fatty acid biosynthesis, and a microalgal lipid droplet

102 high-resolution structural information about fatty acid biosynthesis, and a new strategy is required

103 ic pathways, primary bile acid biosynthesis, fatty acid biosynthesis, and biosynthesis of unsaturated

104 se, the major enzyme required for endogenous fatty acid biosynthesis, and carcinoma lines are growth

105 and cell cycle progression, anti-apoptotic, fatty acid biosynthesis, and endoplasmic reticulum stres

106 colysis, the tricarboxylic acid (TCA) cycle, fatty acid biosynthesis, and nucleotide biosynthesis.

107 ght into the regulation of a crucial step in fatty acid biosynthesis, and provide a plausible explana

108 espiration (aerobic and anaerobic), genes of fatty acid biosynthesis, and the principal genes of amin

109 he pentose phosphate pathway, nucleotide and fatty acid biosynthesis, and the tricarboxylic acid cycl

110 DAF-18/PTEN, AMP-activated kinase and fatty acid biosynthesis are also involved.

111 But whereas the intermediates in fatty acid biosynthesis are fully reduced to generate un

112 xy-3-methylglutaryl-coenzyme A reductase and fatty acid biosynthesis are known to be inhibited by the

113 cyl carrier protein (ACP) and the enzymes of fatty acid biosynthesis are unknown.

114 s, and they suggest how microbes could alter fatty acid biosynthesis as an immune evasion mechanism.

115 t pathway analyses identified coenzyme A and fatty acid biosynthesis as biological processes related

116 m the SREBP-1c-mediated regulation of common fatty acid biosynthesis, as well as by peptide uptake an

117 regulation, metabolism of alpha-glucans, and fatty acid biosynthesis, as well as genes affecting cell

118 identified genes involved in cholesterol and fatty acid biosynthesis, as well as genes involved in fa

119 , which blocked growth through inhibition of fatty acid biosynthesis at the FabI step.

120 cc2 background, because when ACC2 is absent, fatty acid biosynthesis becomes dependent on translation

121 oited for fuel and chemical production, with fatty-acid biosynthesis (beta-ketoacyl-ACP synthases) at

122 have previously shown that the difference in fatty acid biosynthesis between cancer and normal cells

123 have shown previously that the difference in fatty acid biosynthesis between cancer and normal cells

124 enzyme that catalyzes the committed step in fatty acid biosynthesis: biotin-dependent conversion of

125 tually divided into two blocks of reactions (fatty acid biosynthesis (Block A), lipid assembly (Block

126 enzymes FabA and FabZ catalyze a key step in fatty acid biosynthesis; both dehydrate hydroxyacyl fatt

127 ith acidic environments (F1F0-ATPase system, fatty acid biosynthesis, branched chain amino acids meta

128 fragment increases mRNAs encoding enzymes of fatty acid biosynthesis, but not sterol or isoprenoid bi

129 o detected in vivo by monitoring the rate of fatty acid biosynthesis by [(14)C]acetate labeling of ce

130 The first elongation step of fatty acid biosynthesis by a type II dissociated fatty a

131 e III step contributes to the attenuation of fatty acid biosynthesis by acyl-ACP.

132 SIII) initiates straight- and branched-chain fatty acid biosynthesis by catalyzing the decarboxylativ

133 ases provide the building blocks for de novo fatty acid biosynthesis by fatty acid synthase I (FAS I)

134 Applying this approach to study the rates of fatty acid biosynthesis by single cells of S. aureus gro

135 Initiation of straight-chain fatty acid biosynthesis by the type II FAS involves a di

136 Enoyl-ACP reductases participate in fatty acid biosynthesis by utilizing NADH to reduce the

137 X operon or substantive direct regulation of fatty acid biosynthesis by VicR or VicR-P.

138 olites that are generated or utilized during fatty acid biosynthesis can significantly influence gene

139 The long-chain (>=C(20)) polyunsaturated fatty acid biosynthesis capacity of fish varies among sp

140 The genes encoding the components of type II fatty acid biosynthesis cluster at a single location wit

141 expressed candidate genes for straight-chain fatty acid biosynthesis confirmed their role in acylsuga

142 d with lipid droplets and that inhibitors of fatty acid biosynthesis decreased VLS formation or viral

143 lar level of malonyl-CoA, an intermediate in fatty acid biosynthesis, depends on its rate of synthesi

144 Consistent with an increased fatty acid biosynthesis, determination of fat in the liv

145 n biotin biosynthesis, protein synthesis and fatty acid biosynthesis, DNA repair, electron transfer,

146 panded gene families involved in unsaturated fatty acid biosynthesis, DNA repair, photoprotection, io

147 de novo fatty acid biosynthesis (DNFA) is a hallmark adaptation

148 ges of infection, suggesting a late role for fatty acid biosynthesis during HCMV replication.

149 e transcription of genes encoding enzymes of fatty acid biosynthesis, e.g. fatty-acid synthase (FAS).

150 -ACP substrate bound to the Escherichia coli fatty acid biosynthesis enoyl reductase enzyme (FabI), b

151 ethylglutaryl-CoA (HMG-CoA) synthase and the fatty acid biosynthesis enzyme FabH, allow assignment of

152 adjacent to the active site cavities of the fatty acid biosynthesis enzymes and the high degree of s

153 ive expression analysis of 35 genes encoding fatty acid biosynthesis enzymes showed that fatty acid d

154 SpoT monitors fatty acid biosynthesis (FAB), since following cerulenin

155 The fatty acid biosynthesis (FAS-II) pathway in Mycobacteriu

156 tep in the elongation cycle of the bacterial fatty acid biosynthesis (FAS-II) pathway.

157 ey enzymes involved in the type II bacterial fatty acid biosynthesis (FASII) pathway and are putative

158 that the fasamycins inhibit FabF of type II fatty acid biosynthesis (FASII).

159 DX1 in redox metabolism and carbohydrate and fatty acid biosynthesis, for FDX2 in anaerobic metabolis

160 mal peptide synthase family, and mycolic and fatty acid biosynthesis gene families were disproportion

161 ene, encoding a transcriptional regulator of fatty acid biosynthesis genes, contained 54.5% of these

162 Although the critical role of ACP in fatty acid biosynthesis has been established, the role o

163 (MCAT), a mitochondrial protein involved in fatty acid biosynthesis, has now been identified as resp

164 h a number of potent inhibitors of microbial fatty acid biosynthesis have been discovered, few of the

165 Acyl carrier proteins involved in fatty acid biosynthesis have been shown to exhibit a hig

166 Dihomo-gamma-linolenic acid also inhibited fatty acid biosynthesis in 3T3-L1 preadipocytes and sele

167 Although coordination of astaxanthin and fatty acid biosynthesis in a stoichiometric fashion was

168 Fatty acid biosynthesis in alpha- and gamma-proteobacter

169 es the first committed and regulated step in fatty acid biosynthesis in bacteria and thus is a prime

170 n when compared with other Kas inhibitors of fatty acid biosynthesis in bacteria.

171 sation reaction in the initiation of type II fatty acid biosynthesis in both Gram-positive and Gram-n

172 to identify potential feedback regulation of fatty acid biosynthesis in Brassica napus embryo-derived

173 arter units for straight- and branched-chain fatty acid biosynthesis in cell extracts of Streptomyces

174 of genes encoding enzymes of cholesterol and fatty acid biosynthesis in cultured cells.

175 ere is an associated increase in the rate of fatty acid biosynthesis in DENV-infected cells, and de n

176 nection between the regulator of unsaturated fatty acid biosynthesis in E. coli, FabR, thioesterase e

177 Cholesterol and fatty acid biosynthesis in hepatocytes declined by 75%.

178 ion of genes encoding enzymes of unsaturated fatty acid biosynthesis in liver.

179 s in turn is predicted to lower the rates of fatty acid biosynthesis in liver.

180 arrier proteins (ACPs) are the scaffolds for fatty acid biosynthesis in living systems, rendering the

181 he entire coordinated program of unsaturated fatty acid biosynthesis in mouse liver.

182 step reaction that initiates the pathway of fatty acid biosynthesis in plants and bacteria.

183 the first and committed reaction of de novo fatty acid biosynthesis in plastids.

184 scriminates against the streptomycete ACP of fatty acid biosynthesis in preference to RedQ, an ACP of

185 consistent with previous in vivo analyses of fatty acid biosynthesis in S. collinus, which suggested

186 Whereas only WRI1 activates fatty acid biosynthesis in seeds for triacylglycerol pro

187 In the current model of medium-chain (C8-14) fatty acid biosynthesis in seeds, specialized FatB acyl-

188 otein reductase enzyme FabI is essential for fatty acid biosynthesis in Staphylococcus aureus and rep

189 initiating both straight- and branched-chain fatty acid biosynthesis in Streptomyces and that the rat

190 diated transformation of fibroblasts induces fatty acid biosynthesis in the absence of significant ch

191 nses acetyl-CoA with malonyl-ACP to initiate fatty acid biosynthesis in the dissociated, type II fatt

192 nfirm the earlier speculation that elevating fatty acid biosynthesis in the leaf would lead to an inc

193 uted throughout North America and implicates fatty acid biosynthesis in the pathogenesis of macular d

194 yl-ACP synthase III (KASIII) which initiates fatty acid biosynthesis in the type II dissociable fatty

195 Inhibition of fatty acid biosynthesis in these cells resulted in progr

196 itor, cerulenin, markedly reduces tumor cell fatty acid biosynthesis in vivo; (d) fatty acid synthase

197 ns in ACC1 and FAS1, two genes important for fatty acid biosynthesis in yeast; ACC1 encodes acetyl co

198 ns localize to plastids, the site of de novo fatty-acid biosynthesis in plant cells.

199 yl-ACP thioesterase (OTE), another enzyme of fatty acid biosynthesis, in both tissues.

200 boxylase (ACC), the key regulatory enzyme in fatty acid biosynthesis, in the arcuate nucleus (Arc) an

201 The location of the fatty acid biosynthesis inhibitor, cerulenin, that posse

202 fatty acids is blocked by the addition of a fatty acid biosynthesis inhibitor, the organism is rende

203 ells treated with either excess SCFAs or the fatty acid biosynthesis inhibitors cerulenin and 5-(tetr

204 Several of these fatty acid biosynthesis inhibitors have potential as lea

205 ate that this enzyme has a universal role in fatty acid biosynthesis, irrespective of the plant speci

206 Given that elevated fatty acid biosynthesis is a hallmark of many cancers an

207 Unsaturated fatty acid biosynthesis is a vital facet of Escherichia

208 Fatty acid biosynthesis is an essential component of met

209 nes, showed that the expression of genes for fatty acid biosynthesis is elevated in PI126449 glands,

210 Fatty acid biosynthesis is essential for bacterial survi

211 Fatty acid biosynthesis is essential for the survival of

212 s been replaced and the essential process of fatty acid biosynthesis is initiated by plasmid-based ex

213 Fatty acid biosynthesis is transcriptionally regulated b

214 ating the transcription of genes involved in fatty acid biosynthesis is unknown.

215 loroplast accD locus, which is necessary for fatty acid biosynthesis, is essential in Arabidopsis but

216 , mtACP, as a key component of mitochondrial fatty acid biosynthesis, is important in generating the

217 which encodes the rate-controlling enzyme of fatty acid biosynthesis, is shown to be regulated by cel

218 Enoyl reductase (ENR), an enzyme involved in fatty acid biosynthesis, is the target for antibacterial

219 ACC catalyzes the first step in de novo fatty acid biosynthesis known to be downstream of the SR

220 oteins encoded in O-island 138, a cluster of fatty acid biosynthesis-like genes located adjacent to a

221 e cobamides biosynthesis, sterol metabolism, fatty acid biosynthesis, lipid metabolism, carotenoid me

222 imiting enzyme in long-chain polyunsaturated fatty acid biosynthesis, mediates the signature pattern

223 as targeted to the stroma of plastids, where fatty acid biosynthesis occurs.

224 ction of ACC, the rate-controlling enzyme of fatty acid biosynthesis, occurs in the liver in response

225 (i.e., FabG, FabZ, and FabI) involved in the fatty acid biosynthesis of P. falciparum.

226 l carrier protein (ACP), which allows native fatty acid biosynthesis of the Escherichia coli host to

227 bacterial metabolism is primarily fueled by fatty acids, biosynthesis of sugars from intermediates o

228 FabH-independent pathway for straight-chain fatty acid biosynthesis operates in S. glaucescens.

229 gene expression of other enzymes involved in fatty acid biosynthesis or of SREBP-1c.

230 d in TAG biosynthesis than genes involved in fatty acid biosynthesis or other lipid pathways.

231 trols the transcription of genes involved in fatty acid biosynthesis, our results reveal a unique reg

232 cancer, TGF-beta signaling, FoxO signaling, fatty acid biosynthesis, p53 signaling and apoptosis.

233 tase, FabI, is a key enzyme in the bacterial fatty acid biosynthesis pathway (FAS II).

234 The P. falciparum type II fatty acid biosynthesis pathway (PfFAS-II) has been foun

235 al structures for the enzymes of the type II fatty acid biosynthesis pathway can now be exploited in

236 the elongation-condensing enzyme FabF of the fatty acid biosynthesis pathway in bacteria.

237 The fatty acid biosynthesis pathway is an attractive but sti

238 Altogether, we demonstrate that fatty acid biosynthesis pathway manipulation can help ov

239 ase enzyme in the Mycobacterium tuberculosis fatty acid biosynthesis pathway, we predicted its possib

240 icarboxylic acid cycle and its efflux to the fatty acid biosynthesis pathway.

241 acylated acyl carrier protein (ACP) from the fatty acid biosynthesis pathway.

242 uction of key enzymes of the cholesterol and fatty acid biosynthesis pathways, and thus membrane lipi

243 ses; among these are inhibitors of bacterial fatty acid biosynthesis, peptidoglycan synthesis, and di

244 Consistent with a role in de novo fatty acid biosynthesis, pfKASIII exhibited typical KAS

245 f biosynthetic pathways in Escherichia coli: fatty acid biosynthesis, phospholipid biosynthesis, lipo

246 coenzyme A carboxylase (ACCase) function and fatty acid biosynthesis, plants with reduced or increase

247 Therefore we propose a model in which fatty acid biosynthesis plays a central role in regulati

248 insights through quantitative exploration of fatty acid biosynthesis processes for optimal biofuels,

249 A carrying fatty acids reduced the amount of fatty acid biosynthesis proteins to the same extent as p

250 the discovery of two genes encoding Type II fatty acid biosynthesis proteins: ACP (acyl carrier prot

251 ductase catalyses the last reductive step of fatty acid biosynthesis, reducing an enoyl acyl carrier

252 ductase catalyses the last reductive step of fatty acid biosynthesis, reducing the enoyl group of a g

253 and that drugs that regulate cholesterol and fatty acid biosynthesis regulate the replication of the

254 An ideal target for metabolic engineering, fatty acid biosynthesis remains poorly understood on a m

255 duct inhibitors of the condensation steps in fatty acid biosynthesis, represent new classes of compou

256 The FabR (fatty acid biosynthesis repressor) transcriptional repre

257 tiation and elongation condensing enzymes of fatty acid biosynthesis respectively.

258 characterization of the viral modulation of fatty acid biosynthesis revealed that a key enzyme in th

259 n implicated as a physiological inhibitor of fatty acid biosynthesis since acyl-ACP degradation by th

260 he level of malonyl-CoA (the intermediate of fatty acid biosynthesis) specifically in the Arc and inc

261 e level of palmitoyl-CoA (a major product of fatty acid biosynthesis) specifically in the PVN.

262 Pharmacological inhibition of fatty acid biosynthesis suppressed the replication of bo

263 oorganisms, are made by a process resembling fatty acid biosynthesis that allows the suppression of r

264 represses genes involved in cholesterol and fatty acid biosynthesis that are transcriptionally regul

265 zymatic function for M. tuberculosis CitE in fatty acid biosynthesis that is analogous to bacterial c

266 his mutant lacks FabH, an enzyme involved in fatty acid biosynthesis that previously was thought to b

267 arboxylase (ACC) catalyzes the first step of fatty acid biosynthesis, the synthesis of malonyl-CoA fr

268 ependently; one is in fabZ, a dehydratase in fatty acid biosynthesis; the other is in thrS, the Thr-t

269 WRI1 target genes involved in glycolysis and fatty acid biosynthesis; these genes were down-regulated

270 pantothenamides is due to the inhibition of fatty acid biosynthesis through the formation and accumu

271 MV targets ACC1, the rate-limiting enzyme of fatty acid biosynthesis, through multiple mechanisms.

272 s associate with acyl-ACP as a mechanism for fatty acid biosynthesis to coordinate the expression, Fe

273 gent response enzyme SpoT appears to monitor fatty acid biosynthesis to govern transmission trait exp

274 This functional redundancy allows limited fatty acid biosynthesis to occur in the absence of heter

275 proteins (plastid-localized intermediates of fatty acid biosynthesis) to release 3-ketoacids and that

276 terol homeostasis, ApoA-I/ABCA1 pathway, and fatty acid biosynthesis/triglyceride metabolism.

277 etabolism, Porstmann et al. demonstrate that fatty acid biosynthesis, under the transcriptional contr

278 ), a key enzyme initiating bacterial type II fatty acid biosynthesis, usually involve incubation of r

279 ntiseptic triclosan, which are inhibitors of fatty acid biosynthesis, validates this pathway as a tar

280 of 9 has been confirmed to be inhibition of fatty acid biosynthesis via inhibition of FabI.

281 ein (ACP) synthase involved in mitochondrial fatty acid biosynthesis was also identified.

282 The primitiveness of contemporary fatty acid biosynthesis was evaluated by using the therm

283 This oncogene-induced activation of fatty acid biosynthesis was found to be mammalian target

284 sis of central pathway architecture, E. coli fatty acid biosynthesis was re-cast into three modules:

285 conversion of malonyl-CoA to malonyl-ACP for fatty acid biosynthesis was shown to be active with TcmM

286 AcpP, which supports fatty acid biosynthesis, was also a good substrate in th

287 tive in producing primers for branched-chain fatty acid biosynthesis, was bypassed with one of a seri

288 coli acyl carrier protein (ACP), involved in fatty acid biosynthesis, was not bound to DltD and thus

289 accumulation of intermediate metabolites of fatty acid biosynthesis, we then questioned whether prot

290 acetyl-phosphate and subsequently leading to fatty acid biosynthesis were consistently upregulated du

291 fast light-responding genes in, for example, fatty acid biosynthesis were identified and allocated to

292 Proportions of bacterial genes involved in fatty acid biosynthesis were lower in feces from patient

293 acyl-acyl-carrier-proteins (intermediates in fatty acid biosynthesis) were hydrolyzed and decarboxyla

294 anges in proteins and transcripts related to fatty acid biosynthesis, whereas proteins and transcript

295 ly distinct from all known ketoreductases of fatty acid biosynthesis, which instead belong to the sho

296 els for known SREBP target genes involved in fatty acid biosynthesis, which led to significantly high

297 One such pathway is fatty acid biosynthesis, whose induction is observed upo

298 ied out the initial condensation reaction of fatty acid biosynthesis with acetyl-coenzyme A (acetyl-C

299 emcitabine responsiveness upon inhibition of fatty acid biosynthesis with orlistat.

300 l-CoA carboxylase (ACC) and thereby inhibits fatty acid biosynthesis with submicromolar potency.