ライフサイエンスコーパス: biosynthesis

1 for ER body formation and MYB51/122 for IGs biosynthesis).

2 nesis pathway that lead to impaired cortisol biosynthesis.

3 suppression of pigment; and (3) Fe/S cluster biosynthesis.

4 to inappropriate derepression of cholesterol biosynthesis.

5 its regulator, CrMYC2, play key roles in TIA biosynthesis.

6 substrates and cofactors required for lignin biosynthesis.

7 ion, leukocyte extravasation and cholesterol biosynthesis.

8 ential regulatory role of ACPS in fatty acid biosynthesis.

9 bit MurA, which is involved in peptidoglycan biosynthesis.

10 reserved for re-initiation of peptidoglycan biosynthesis.

11 ucleases, nickel/cobalt uptake and cobalamin biosynthesis.

12 biosynthesis and degradation, and bile acid biosynthesis.

13 s regulating genes associated with flavonoid biosynthesis.

14 6s evolved specifically towards triterpenoid biosynthesis.

15 ECs and VSMCs, potentially facilitating SPM biosynthesis.

16 to block serine hydrolases involved in their biosynthesis.

17 leading to the tissue-specific triterpenoid biosynthesis.

18 e organization of later steps in chlorophyll biosynthesis.

19 ctors and CYPs related to camptothecin (CPT) biosynthesis.

20 transferase involved in heparan sulfate (HS) biosynthesis.

21 rowth, suggesting these compounds inhibit MK biosynthesis.

22 egradation rate, resulting in higher net Cys biosynthesis.

23 lipofuscin) via upregulation of cholesterol biosynthesis.

24 on glucose metabolism to fuel macromolecule biosynthesis.

25 dient can be established independently of GA biosynthesis.

26 for the further elucidation of mycofactocin biosynthesis.

27 lated to fiber elongation and secondary wall biosynthesis.

28 ved aspartate to maintain de novo pyrimidine biosynthesis.

29 ent inhibition of de novo thymidylate (dTMP) biosynthesis.

30 rated that it controls folate and ubiquinone biosynthesis.

31 central metabolite for membrane phospholipid biosynthesis.

32 ed sugar provides carbon skeletons for lipid biosynthesis.

33 me in the guanylate branch of de novo purine biosynthesis.

34 uring the growing season promoted carotenoid biosynthesis.

35 generation and uncouple NADH generation from biosynthesis.

36 o regain completely its ability of aflatoxin biosynthesis.

37 rogenase, an enzyme essential for pyrimidine biosynthesis.

38 nCL proteins are not involved in lanthionine biosynthesis.

39 of translation, fermentation, and amino acid biosynthesis.

40 rix octapeptidase Oct1p and coenzyme Q (CoQ) biosynthesis-a pathway essential for mitochondrial respi

41 vitamin B6, we investigate the regulation of biosynthesis across eudicot and monocot species under he

42 program involving Myc activation and sterol biosynthesis after M-CSF stimulation.

43 t of various types of plastids on carotenoid biosynthesis and accumulation, and discuss recent advanc

44 ausible regulatory role for NnCYP76B6 in CPT biosynthesis and also establish a valuable repository fo

45 gulation of enzymes involved in both protein biosynthesis and biosynthetic pathways, as well as of se

46 B12 depletion, which suppresses de novo dTMP biosynthesis and causes DNA damage, accounting for the p

47 ined by two complementary processes: biomass biosynthesis and cell expansion.

48 cadian clock signaling on rates of cellulose biosynthesis and cell wall biomechanics.

49 metabolism, phenylalanine metabolism, lysine biosynthesis and degradation, and bile acid biosynthesis

50 cycle and depend on the balance between dNTP biosynthesis and degradation.

51 Recombinant irisin stimulated insulin biosynthesis and glucose-stimulated insulin secretion (G

52 ight act as crucial regulators for flavonoid biosynthesis and glycolysis, respectively.

53 roxylase (CYP11B1), which catalyzes cortisol biosynthesis and is highly homologous to CYP11B2, is unc

54 hanism involving adipocyte-dependent uridine biosynthesis and leptin signaling.

55 are redundantly required for functional RMA biosynthesis and male meiotic cytokinesis.

56 on metabolism, which is essential for purine biosynthesis and methionine recycling and affects methyl

57 abolism, methionine and S-adenosylmethionine biosynthesis and methionine salvage, and signs of altere

58 ing of the molecular basis underlying lignin biosynthesis and perturbation in grasses.

59 ous organisms, yet little is known about its biosynthesis and physiological functions.

60 Although several steps in MPO biosynthesis and processing have been elucidated, many q

61 arch biosynthesis, lipid metabolism, protein biosynthesis and processing.

62 related with plant defense systems, hormone biosynthesis and response were particularly enriched.

63 regulated by SA and P. syringae, enhances SA biosynthesis and SA signalling responses; e.g. in respon

64 with actions including regulation of insulin biosynthesis and secretion, promotion of satiety, and pr

65 iR response reveals a modulation in ethylene biosynthesis and signaling, metal ions deficiency respon

66 ross talk between the activation of stilbene biosynthesis and the accumulation of anthocyanins in rip

67 in intermediate steps of terpenoid backbone biosynthesis and those related to secondary transformati

68 al drug by which modulation of neural glycan biosynthesis and thus function can be achieved in vivo.

69 0-methylenetetrahydrofolate for de novo dTMP biosynthesis and translocate to the nucleus during S-pha

70 tal pathways as regulation of transcription, biosynthesis and transport of lipids, hormone-mediated s

71 gh leaf vein density requires elevated auxin biosynthesis and transport.

72 The biosynthesis and utilization of enterobactin permits man

73 demonstrate the proviral role of PLK1 in HBV biosynthesis and validate PLK1 inhibition a potential an

74 been previously associated with gonadotropin biosynthesis and/or secretion.

75 nctional interaction with BasA (sphingolipid biosynthesis) and StoA (apical sterol-rich membrane doma

76 e receptor activity, chemotaxis and cytokine biosynthesis, and angiogenesis and vascular development

77 storing normal ATP production, macromolecule biosynthesis, and growth.

78 howed that exogenous pABA is used for folate biosynthesis, and leads to decreased stress and elevated

79 hich stimulates protein, lipid, and ribosome biosynthesis, and mTORC2, which regulates cytoskeleton f

80 n lead to metabolic alterations of terpenoid biosynthesis, and show that these transgenic plants have

81 ne, yqiC, which is required for efficient UQ biosynthesis, and which we have renamed ubiK Using sever

82 inhibited; conversely, glycolysis and lipid biosynthesis are curtailed as sugar levels decrease and

83 th the chemical diversity in natural product biosynthesis as well as the parallels with synthetic org

84 tions, including morphogenesis and cell wall biosynthesis, as well as the activity of the cell integr

85 he observed differences in oligogalactolipid biosynthesis between the two species, we suggest that ex

86 growth and development of fungus, aflatoxin biosynthesis, binding, transport, and signaling were ide

87 , or of purF alone, abolished de novo purine biosynthesis but did not impact bacterial adherence prop

88 ochondrial AAA+ unfoldase ClpX promotes heme biosynthesis by activation of delta-aminolevulinate synt

89 posal that LanCL1 is involved in lanthionine biosynthesis by constructing LanCL1 knock-out mice and m

90 ith the euphotic zone rather than its direct biosynthesis by primary producers.

91 cellular redox balance, producing NADPH for biosynthesis by recycling the two other primary redox ca

92 PDR1 overexpression allowed considerable SL biosynthesis by releasing SL biosynthetic genes from an

93 ate a possible interference of selenoprotein biosynthesis by the antibiotics and elucidate potential

94 allows cells to maintain a stable rate of RA biosynthesis by utilizing a biological circuit generated

95 activity of aminoglycosides on selenoprotein biosynthesis can be severe, but depend on the Se status,

96 iD enzyme, which is implicated in ubiquinone biosynthesis, cannot be isolated in an active holoenzyme

97 Vitamin B12 depletion decreased de novo dTMP biosynthesis capacity by 5-35%, whereas de novo purine s

98 er induce multiple stress responses, reduced biosynthesis, cell viability and growth; and (6) ethanol

99 ng pathways, defense response, glucosinolate biosynthesis, cell wall modification, sugar transport, a

100 f genes related to phenylpropanoid/flavonoid biosynthesis clearly distinguished the behavior of red a

101 e gene, the first committed step in ethylene biosynthesis compared with wild type.

102 In conclusion, NAPRT-dependent NAD(+) biosynthesis contributes to cell metabolism and to the D

103 nd CTPS, which regulate flux into pyrimidine biosynthesis, correlates with better prognosis in pancre

104 ground absence of cpsA reduces and delays ST biosynthesis decreasing the expression of ST genes.

105 tinal degeneration associated with rhodopsin biosynthesis defects, while frameshift phenotypes were c

106 anscriptional target, AKAP10, regulates heme biosynthesis during erythropoiesis at the outer mitochon

107 erial strains in which modified carbohydrate biosynthesis enzymes have been knocked out, we are devel

108 seed proteins, such as storage proteins, oil biosynthesis enzymes, and transcription factors, reside

109 nt analysis identified redundancy in several biosynthesis families, we found that mutation of LjIpt4

110 osynthesis, sesquiterpenoid and triterpenoid biosynthesis for protective cuticle and wax.

111 ection for aerobic glycolysis and uncoupling biosynthesis from NADH generation.

112 equencing and qRT-PCR revealed that arginine biosynthesis genes (argR, argB, argC, argG, argH and arg

113 s defective in AM-specific paralogs of lipid biosynthesis genes (KASI and GPAT6).

114 Co-cultured diatoms also downregulated lipid biosynthesis genes and upregulated chitin metabolism gen

115 An analysis of the expression of terpenoid biosynthesis genes confirmed that the MeJA application a

116 This, along with the upregulation of JA-biosynthesis genes in inoculated bark and core tissues f

117 ctive differences, with upregulation of heme biosynthesis genes prominently in RP-mediated DBA and fa

118 eukaryotes shared functionally modern sterol biosynthesis genes with bacteria via horizontal gene tra

119 Moreover, the mRNA levels of three ABA biosynthesis genes, ABA1, NCED9, and AAO3, and three ABA

120 oinduction of anaerobic genes and ergosterol biosynthesis genes, biosynthesis of basic amino acids, a

121 ed core of RbkR regulons includes riboflavin biosynthesis genes, known/predicted vitamin uptake trans

122 ons, little polymorphism was found in folate biosynthesis genes.

123 of those are involved in glucosinolate (Gl) biosynthesis, glycosylated sulphur-containing aldoximes

124 Since NO biosynthesis has been related to polyamine metabolism, w

125 d, the regulatory components controlling its biosynthesis have not been definitively determined.

126 n it is co-expressed with genes encoding PEB biosynthesis (i.e. ho1 and pebS).

127 lism or disruption of Myc function or sterol biosynthesis impaired myeloid differentiation.

128 deficiency on cuticle formation in three ABA biosynthesis-impaired tomato mutants.

129 We conclude that selection for high rate of biosynthesis implies a selection for aerobic glycolysis

130 s, positively regulates glycolysis and lipid biosynthesis in Arabidopsis thaliana Here, we identify m

131 Quantification of nucleotide biosynthesis in ATR-inhibited acute lymphoblastic leukem

132 is well-defined, the mechanisms driving its biosynthesis in cancer are poorly understood.

133 ioning in support of storage oil and protein biosynthesis in developing COS.

134 A system reconstituting bilin biosynthesis in Escherichia coli was modified to utilize

135 We analyzed HK biosynthesis in human leukocytes stimulated ex vivo and

136 ese results show the importance of cytokinin biosynthesis in initiating and balancing the requirement

137 hanisms of IgM assembly, we investigated its biosynthesis in living cells and faithfully reconstitute

138 On the basis of genomic analyses, cobalamin biosynthesis in marine systems has been inferred in thre

139 tant gene contributing hybrid vigor in lipid biosynthesis in oil palm.

140 Carotenoid biosynthesis in plants includes a complex series of desa

141 rotenogenic enzymes in modulating carotenoid biosynthesis in plants.

142 SE (STS) are the enzymes responsible for RFO biosynthesis in plants.

143 ffect of different pathways of phenylalanine biosynthesis in Pseudomonas sp.

144 ofiling marked suppression of glucocorticoid biosynthesis in the epidermis of psoriatic skin leading

145 ge of phenomena that accompanies anthocyanin biosynthesis in tomato, including adaptions of the plant

146 in critical yet missing steps of astaxanthin biosynthesis, including ABC transporters, cytochrome P45

147 yb60 can activate pathways beyond monolignol biosynthesis, including those that synthesize the substr

148 trate that PGC1alpha alone can support viral biosynthesis independently of the expression of addition

149 ment with either brassinolide (BL) or the BR biosynthesis inhibitor brassinazole (BRZ).

150 utility of abiraterone acetate, an androgen biosynthesis inhibitor, in the early treatment of metast

151 ynthesis mutant, aos, or upon addition of JA biosynthesis inhibitors.

152 accumulated higher levels of the chlorophyll biosynthesis intermediate Mg-protoporphyrin IX monomethy

153 lts in pathological accumulation of the heme biosynthesis intermediate protoporphyrin IX (PPIX).

154 tes several key activities in polysaccharide biosynthesis into a single polypeptide.

155 any steady-state condition by projecting all biosynthesis into three measurable variables representin

156 veness of these genes confirm that cytokinin biosynthesis is a key target of the common symbiosis pat

157 dependent nuclear de novo thymidylate (dTMP) biosynthesis is a sensitive target of arsenic trioxide (

158 In the absence of veA (DeltaveA), ST biosynthesis is blocked.

159 The first specific step in PA biosynthesis is catalyzed by homospermidine synthase (HS

160 ine and agriculture, but regulation of their biosynthesis is incompletely understood.

161 Plant terpene biosynthesis is regulated at multiple levels, leading to

162 it has remained unclear whether and how its biosynthesis is regulated by the symbiotic pathway.

163 is model, we demonstrate that glucocorticoid biosynthesis is suppressed by proinflammatory cytokines

164 Frontline antibiotics inhibit mycomembrane biosynthesis, leading to rapid cell death.

165 to demonstrate that tellurite inhibits heme biosynthesis, leading to the accumulation of intermediat

166 lycolysis/gluconeogenesis, TCA cycle, starch biosynthesis, lipid metabolism, protein biosynthesis and

167 te its relevant role in extracellular matrix biosynthesis, little is known about the structural requi

168 nd suggest that channeling serine into lipid biosynthesis may not be a cardinal cellular function of

169 of great importance for understanding lignin biosynthesis mechanism and developing lignin based chemi

170 Thermomorphogenesis requires increased auxin biosynthesis, mediated by the bHLH transcription factor

171 JA receptor mutant, coi1, but not in the JA biosynthesis mutant, aos, or upon addition of JA biosynt

172 lipases (DAGLs), enzymes responsible for the biosynthesis of 2-arachidonoylglycerol (2-AG) that activ

173 synthase (QueE) catalyzes a key step in the biosynthesis of 7-deazapurine containing natural product

174 bridged the missing links in the early-stage biosynthesis of ambiguines.

175 Two gene clusters involved in the biosynthesis of an allelochemical 2,4-dihydroxy-7-methox

176 m lycopersicum) for coordinated induction of biosynthesis of anthocyanins, in a tissue- and developme

177 chrysin and apigenin and is responsible for biosynthesis of baicalein and scutellarein in roots and

178 bic genes and ergosterol biosynthesis genes, biosynthesis of basic amino acids, and several stress ge

179 family and shedding critical light onto the biosynthesis of bioactive stilbenoids.

180 50 family in secondary modifications for the biosynthesis of bioactive triterpenoids.

181 minase BioA catalyzes the second step in the biosynthesis of biotin in Mycobacterium tuberculosis (Mt

182 Insights into the biosynthesis of crochelins and the mechanism by which ir

183 methylase is a key enzyme intermediating the biosynthesis of ergosterol in fungi, and the target of a

184 The biosynthesis of ethylene is highly regulated by a variet

185 ndidate genes associated with caste-specific biosynthesis of fatty acid pheromones in the MG, includi

186 These data suggest that the biosynthesis of flavan-3-ols in potato tuber would requi

187 and fruit and probable participation in the biosynthesis of fruit-specific triterpenoids.

188 f 5-lipoxygenase and cyclooxygenase-2 in the biosynthesis of hemiketals E2 and D2 by activated human

189 EXTL3 regulates the biosynthesis of heparan sulfate (HS), important for both

190 em and xylem might contribute to the de novo biosynthesis of JA after fungal infection.

191 n inhibiting the first committed step in the biosynthesis of lipid A, the deacetylation of uridyldiph

192 scriptional control of genes involved in the biosynthesis of maize phenolic compounds including gener

193 ls and also a prime donor of nitrogen in the biosynthesis of many amino acids.

194 The biosynthesis of many eukaryotic proteins requires accura

195 enzymes responsible for the "assembly line" biosynthesis of many genetically encoded small molecules

196 ication of the CYP450s genes involved in the biosynthesis of MG secretions, we analyzed by means of q

197 spite recent progress, the mechanism for the biosynthesis of most modifications is not fully understo

198 iae can be engineered to perform the complex biosynthesis of multicellular fungi, opening up the poss

199 amolecular C-C cross-linking reaction in the biosynthesis of mycocyclosin, is crucial for the viabili

200 Results suggest signaling and biosynthesis of NDCs change dramatically as a function o

201 ER stress leads to de novo biosynthesis of non-trimethylated GRP78, whereas homeost

202 re important for responses to stress and the biosynthesis of numerous essential compounds.

203 modifications to systematically unravel the biosynthesis of one of the most densely modified and met

204 Biosynthesis of OXT-A has been linked to a plasmid-borne

205 ation of Andean potato was used to study the biosynthesis of phenolic compounds.

206 y carbon substrate for energy production and biosynthesis of phospho-sugars, nucleobases, peptidoglyc

207 E1 (HY1) that encodes the key protein in the biosynthesis of phytochromobilin, a cofactor of photocon

208 The biosynthesis of polytheonamides involves up to 50 site-s

209 it offers novel insight into the engineered biosynthesis of prenylated natural products.

210 How the biosynthesis of PtdIns(4,5)P2 by phosphatidylinositol 4-

211 verall, these data identify key steps in the biosynthesis of pyrethrins and demonstrate the feasibili

212 from photosynthesis are used to support the biosynthesis of secondary metabolites, while the compara

213 ns or components may be required for in vivo biosynthesis of SFTI-1.

214 -phosphate dehydrogenase, the key enzyme for biosynthesis of sorbitol.

215 miRNAs in posttranscriptional control of the biosynthesis of specialized metabolites.

216 sity and distributions of genes encoding the biosynthesis of specialized metabolites.

217 cus on the [4 + 2] cycloaddition step in the biosynthesis of spinosyn A, a reaction catalyzed by SpnF

218 d contusion injury in adult female mice, the biosynthesis of SPM is not induced in the lesion site up

219 51) is a cytochrome P450 enzyme required for biosynthesis of sterols in eukaryotic cells and is the m

220 the crenearchaeon Sulfolobus acidocaldarius, biosynthesis of the archaellum is regulated by regulator

221 nthase (LipA) catalyzes the last step in the biosynthesis of the lipoyl cofactor, which is the attach

222 activity in Arabidopsis thaliana stimulates biosynthesis of the major phospholipid phosphatidylcholi

223 I polyketide synthase (PKS) involved in the biosynthesis of the marginolactone azalomycin F in mangr

224 The biosynthesis of the N. fumigata ergot alkaloids and thei

225 The polyketide synthases responsible for the biosynthesis of the polyether antibiotics nanchangmycin

226 rSAM methyltransferase TbtI involved in the biosynthesis of the potent thiopeptide antibiotic thiomu

227 We hypothesized that biosynthesis of the selenium (Se) transporter selenoprot

228 atible mild aqueous chemistries, synchronous biosynthesis of the tagged metabolite and its subsequent

229 Though biosynthesis of these complex molecules requires substra

230 new developments in the understanding of the biosynthesis of these molecules where dual enzymatic act

231 ne synthases, enabling future studies of the biosynthesis of this important bioactive natural product

232 to formulate a biosynthetic pathway for the biosynthesis of triptolide, a diterpenoid with pharmaceu

233 acetyltransferase enzyme, PglD, involved in biosynthesis of UDP-diNAcBac in Campylobacter jejuni.

234 ct the differing dependence of expansion and biosynthesis on energy, carbon, and water.

235 ites located within two different antibiotic biosynthesis operons.

236 either ketosynthase domains from polyketide biosynthesis or adenylation domains from nonribosomal pe

237 combination therapy primarily targets lipid biosynthesis or effects bioactive lipids that activate s

238 unctional plastids due to defects in pigment biosynthesis or translation are known to repress photosy

239 pacts glycan biosynthesis through Hexosamine Biosynthesis Pathway (HBP), as well as cellular redox ho

240 es and identified 55% with upregulated mtDNA biosynthesis pathway expression compared with normal hem

241 monstrated the presence of an intact de novo biosynthesis pathway for NAD(+) from tryptophan via QA,

242 Menaquinone (MK) biosynthesis pathway is a potential target for evaluatin

243 s Cryptococcus neoformans Because the purine biosynthesis pathway is essential for many metabolic pro

244 Because the heme biosynthesis pathway is highly conserved in eukaryotes,

245 Altogether, we demonstrate that fatty acid biosynthesis pathway manipulation can help overcome the

246 PP) is a rare inherited disorder of the heme biosynthesis pathway resulting in the accumulation of pr

247 isms that exist at every step of the protein biosynthesis pathway, such as alternative splicing and p

248 To better understand the secoiridoid biosynthesis pathway, we generated transcriptome sequenc

249 bA is required in the tetrahydrofolate (THF) biosynthesis pathway.

250 irst enzyme in the branched-chain amino acid biosynthesis pathway.

251 as kauralexin production by the diterpenoid biosynthesis pathway.

252 ical bifurcated hydroxylation process in the biosynthesis pathway.

253 level of the environment regulates the BCAA biosynthesis pathway.

254 lated genes involved in reproductive hormone biosynthesis pathways and provide a framework for future

255 te specificities originate and evolve as new biosynthesis pathways emerge.

256 omal peptides, and transferases from various biosynthesis pathways.

257 lycans, to study processes such as cell wall biosynthesis, polysaccharide deposition, protein-carbohy

258 In Bacillus spp., where PHB biosynthesis precedes the formation of the dormant cell

259 Inspired by an ergothioneine biosynthesis protein EgtB, a mononuclear non-haem iron e

260 , replication-division cycle, and the global biosynthesis rate.

261 es are noncoding and bind Fe(2+) to regulate biosynthesis rates of the encoded, iron homeostatic prot

262 (CAD) catalyzes the final step in monolignol biosynthesis, reducing sinapaldehyde, coniferaldehyde, a

263 erized genes involved in xylan and cellulose biosynthesis, regulators of xylem vessel and fiber diffe

264 homologous to 49 publically-searched rubber biosynthesis related genes.

265 ctrometry analysis, we demonstrated that GAC biosynthesis requires two distinct undecaprenol-linked G

266 transcription factor SREBP and thus of lipid biosynthesis, resulted in significantly retarded CNS mye

267 etabolism pathways including phenylpropanoid biosynthesis, sesquiterpenoid and triterpenoid biosynthe

268 In yeast, mutants defective in sterol biosynthesis show a wide range of changes in transcripti

269 rate-limiting step in 27-hydroxycholesterol biosynthesis, significantly reduces metastasis in releva

270 g organelle-specific regulation of jasmonate biosynthesis; simultaneous induction of synthesis and br

271 ressed CI symptoms and induced more ethylene biosynthesis than the other treatments.

272 l strategy of peptide-nucleotide antibiotics biosynthesis that may help control production levels and

273 ic apparatus and one for phosphatidylcholine biosynthesis, that were not known to be essential for ph

274 The ultimate step in lysine biosynthesis, the NAD(+)-dependent dehydrogenation of sa

275 first and rate-limiting step in sphingolipid biosynthesis: the condensation of serine and palmitoyl-C

276 spite progress in deciphering plant volatile biosynthesis, their release from the cell has been poorl

277 ces a cascade of events which impacts glycan biosynthesis through Hexosamine Biosynthesis Pathway (HB

278 gical processes ranging from natural product biosynthesis through to the mammalian visual cycle.

279 with acyl-ACP as a mechanism for fatty acid biosynthesis to coordinate the expression, Fe-S cofactor

280 s and a corresponding increase in pyrimidine biosynthesis to enhance the intrinsic levels of deoxycyt

281 anding the regulatory network linking lignin biosynthesis to plant growth and defense will help ligni

282 diated by the reprogramming of peptidoglycan biosynthesis to use precursors terminating in D-Ala-D-La

283 tRNA(Cys) synthesis (tRNA-dependent cysteine biosynthesis) to prevent challenge of translational fide

284 Mutations in KDSR cause defective ceramide biosynthesis, underscoring the importance of ceramide an

285 rotein biosynthesis while not inhibiting DNA biosynthesis using (3)H-radiolabeled precursors in macro

286 electively controlling their respective core biosynthesis using CRISPR interference and antibiotics,

287 (TCA) cycle of ECs and contributes to lipid biosynthesis via reductive carboxylation.

288 ing the final enzymatic step in solanapyrone biosynthesis was specifically associated with developmen

289 denylation domains from nonribosomal peptide biosynthesis was used to assess biosynthetic domain comp

290 lly, transcription factors regulating lignin biosynthesis were also up-regulated in resistant plants

291 pts encoding the key enzymes for secoiridoid biosynthesis were examined in different S. mussotii tiss

292 Enzymes of amino acid biosynthesis were higher in coculture than in axenic cul

293 are not known to be involved in anthocyanin biosynthesis were observed to be regulated.

294 sm, including genes implicated in ophiobolin biosynthesis, were identified.

295 es a homeostatic mechanism that favors lipid biosynthesis when intracellular sugar levels are elevate

296 ylase (NnCYP76B6) an important enzyme in CPT biosynthesis which specifically shunts geraniol into the

297 Inhibition of glutathione biosynthesis, which protects cells from reactive metabol

298 HP 1 inhibited RNA and protein biosynthesis while not inhibiting DNA biosynthesis using

299 ycosyltransferase involved in xylan backbone biosynthesis, while UPEX1 encodes a family GT31 glycosyl

300 responsiveness upon inhibition of fatty acid biosynthesis with orlistat.