ライフサイエンスコーパス: biosynthesis

1 ibution in addition to light-dependent auxin biosynthesis.

2 d one-carbon units needed for de novo purine biosynthesis.

3 alyze the first committed step in triterpene biosynthesis.

4 es its expression to promote the anthocyanin biosynthesis.

5 nergy and metabolites as building blocks for biosynthesis.

6 es the complete set of genes to engineer MbA biosynthesis.

7 racterize UGTs putatively involved in SVglys biosynthesis.

8 ion of protein biosynthesis and tetrapyrrole biosynthesis.

9 nding of HBV rcDNA deproteination and cccDNA biosynthesis.

10 or to medications that interfere with sterol biosynthesis.

11 moiety of dehydroabietic acid in triptolide biosynthesis.

12 known which genes control cork triterpenoid biosynthesis.

13 icantly with the early stages of l-histidine biosynthesis.

14 the human body related to biodegradation and biosynthesis.

15 e cancer cells with energy and substrates of biosynthesis.

16 and extracellular substrates into polyketide biosynthesis.

17 dephosphorylation of Orm2, a repressor of SL biosynthesis.

18 l for iron-sulfur cluster formation and heme biosynthesis.

19 single enzyme is sufficient for rhizoferrin biosynthesis.

20 vely regulates genes involved in anthocyanin biosynthesis.

21 cing (PTGS) of the key enzyme of anthocyanin biosynthesis.

22 and genomic aspects of secondary metabolite biosynthesis.

23 on of penicillin substrates in cephalosporin biosynthesis.

24 cur independent of genetic disruption of NAD biosynthesis.

25 ential and/or ATP synthesis impaired proline biosynthesis.

26 ulose synthase like-C (CSLC) proteins in XyG biosynthesis.

27 icient translation initiation during protein biosynthesis.

28 A carboxylase and polyunsaturated fatty acid biosynthesis.

29 is fully assembled and competent in cofactor biosynthesis.

30 nk between disparate cyclases in thiopeptide biosynthesis.

31 r tree, some of which are involved in rubber biosynthesis.

32 essential transformations in natural product biosynthesis.

33 oted optimal GC polarization and cholesterol biosynthesis.

34 ting the fatty acid precursor of lipoic acid biosynthesis.

35 ential critical genes involved in flavonoids biosynthesis.

36 intracellular transport and thereby affects biosynthesis.

37 ously reported to be involved in acylglucose biosynthesis.

38 h encodes a rate-limiting enzyme in ethylene biosynthesis.

39 metabolic pathways to prioritize siderophore biosynthesis.

40 vels of proteins dedicated to metabolism and biosynthesis(1,2).

41 egulation of Pseudomonas aeruginosa alginate biosynthesis(3,4), as a regulator of the expression and

42 RH1 mainly functions as an anthocyanin biosynthesis activator that specifically determines leaf

43 type usage, VDJ sequence, metabolic profile, biosynthesis activity, and signaling response.

44 thesis via the lipoxygenase pathway and IL-2 biosynthesis (all P < .01).

45 ese data provide novel insights into beta-PE biosynthesis and advance our understanding of the mechan

46 ung cell population important for surfactant biosynthesis and alveolar homeostasis.

47 at are known to inhibit cellular cholesterol biosynthesis and are clinically prescribed to patients w

48 module, a regulatory axis composed of auxin biosynthesis and auxin perception factors controls root

49 e metagenomic approach to mine for phenazine biosynthesis and biodegradation genes, applying it to >8

50 Providing further challenges, glycan biosynthesis and cellular behavior are co-regulating sys

51 ing telomere damage, defective mitochondrial biosynthesis and clearance, cell growth retardation, and

52 unique high metabolic flux through polyamine biosynthesis and connected one carbon metabolism in CaP

53 emical analysis showed altered cutin and wax biosynthesis and deposition in fdl1-1 mutant seedlings a

54 eins, the cornerstone to bacterial cell wall biosynthesis and division.

55 r host fitness, and pathways for key vitamin biosynthesis and export were identified across MAGs.

56 and transport processes including cell wall biosynthesis and gene regulation.

57 However, its biosynthesis and genetic distribution remain unknown.

58 of the pathways that contribute to cell wall biosynthesis and how these pathways are regulated by ext

59 t cancer cells by inhibiting de novo proline biosynthesis and impairing spheroidal growth.

60 Conversely, genes for gibberellin biosynthesis and inactivation using methyltransferases a

61 ate] species designated FeMo-cofactor, whose biosynthesis and insertion requires the action of over a

62 Heme biosynthesis and iron-sulfur cluster (ISC) biogenesis ar

63 DA-responsive genes but downregulation of JA biosynthesis and JA response genes.

64 ing expression of genes associated with 5-HT biosynthesis and metabolism.

65 d maize B73 revealed upregulation of 12-OPDA biosynthesis and OPDA-responsive genes but downregulatio

66 plants, suggesting that JMJ14 regulated Pip biosynthesis and other downstream factors regulate SAR i

67 riants in several genes participating in GPI biosynthesis and processing lead to decreased cell surfa

68 lic acid cycle, carbon balance, phytohormone biosynthesis and redox homeostasis.

69 icate deregulated fatty acid and cholesterol biosynthesis and reduced liver X receptor activation wit

70 While the biosynthesis and reduction of trypanothione are cytosoli

71 Biosynthesis and remodeling of the GPI anchor requires t

72 ociated with glycolytic metabolism, collagen biosynthesis and remodeling, redox regulation and immuno

73 n of genes involved in all stages of protein biosynthesis and ribosome biogenesis during both stages

74 abolomics that unravel the interplay between biosynthesis and salvage of vitamins and cofactors in ap

75 ly postulated as we uncovered active de novo biosynthesis and substantial levels of accumulation of p

76 bacterial pathway for 9M5-FuFA and 9D5-FuFA biosynthesis and suggest the existence of homologs of th

77 of tRNA(Glu) at the intersection of protein biosynthesis and tetrapyrrole biosynthesis.

78 duction and is involved in HH103 KPS and LPS biosynthesis and that an HH103 rkpM mutant cannot produc

79 lular localization of the final stage of TPP biosynthesis and the chemical nature of the substrates t

80 ticulum (ER), the main cellular hub of lipid biosynthesis and the entry site for the secretory pathwa

81 and mevalonic acid, sterol, and cholesterol biosynthesis and trafficking/redistribution.

82 monoacylglycerol (2-MAG), and membrane lipid biosynthesis and transport during nodule development.

83 Additionally, we observed that amino acid biosynthesis and transport regulons, controlled by ArgR,

84 Depletion of IIS or TORC1 blocked both JH biosynthesis and vitellogenesis.

85 involved in inhibition of purine nucleotide biosynthesis and with GTPases that control ribosome asse

86 her tRNA(Glu) allocation limits tetrapyrrole biosynthesis and/or protein biosynthesis remains poorly

87 (eg, branched chain amino acids and arginine biosynthesis) and virulence genes (eg, beta-toxin, delta

88 rogenase (GalDH), a key enzyme for vitamin C biosynthesis, and altered the composition of phenolic co

89 gibberellin content, enhanced cutin and wax biosynthesis, and increased fruit firmness and shelf lif

90 t SnRK1 negatively regulates phenylpropanoid biosynthesis, and KFB(PALs) act as regulatory components

91 up-regulating the proline cycle and proline biosynthesis, and knockdowns of PYCR1 lead to decreased

92 struction, biofilm formation, antimicrobials biosynthesis, and metabolism of diverse nutrients.

93 complex interplay among cell-wall expansion, biosynthesis, and, in specific tissues, secondary cell w

94 the molecular basis underlying floral scent biosynthesis; and winter flowering, and highlight the ut

95 ownstream target genes function in cell wall biosynthesis, apoptosis, and maintenance of xylem cell w

96 how that active FA, 2-MAG and membrane lipid biosynthesis are essential for nodulation and rhizobia-s

97 , synthetic gene circuits for organofluorine biosynthesis are implemented in the platform bacterium P

98 The regulatory aspects of cell wall biosynthesis are largely overlapping with those of eudic

99 agenomic pathway analysis identified steroid biosynthesis as the most underrepresented metabolic path

100 Blocking N-glycan biosynthesis at the oligomannose stage using both geneti

101 two competing topological isomers during its biosynthesis at the ribosome-translocon complex.

102 Due to the conserved sterol biosynthesis between mice and humans, we suggest that th

103 inal oxidation step of the hemolytic saponin biosynthesis branch in M. truncatula In addition, two ur

104 hibited severe defects not only in fumonisin biosynthesis but also vegetative growth and conidiation.

105 ibutors to this process, promoting cytokinin biosynthesis but repressing gibberellin production to co

106 B-SIMS) to directly visualize de novo purine biosynthesis by a multienzyme complex, the purinosome.

107 icated that TmMYB3 is involved in paclitaxel biosynthesis by activating the expression of TBT and TS.

108 s leads to inhibition of bacterial cell wall biosynthesis by disassembly of key divisome proteins, th

109 strated that the inhibition of de novo lipid biosynthesis by interfering with nematode ACC is a new n

110 SBG9 functions as a key regulator of cuticle biosynthesis by preferentially regulating expression of

111 In rishirilide biosynthesis by Streptomyces bottropensis, (13)C-labelin

112 Inhibition of trypanothione biosynthesis by the anti-trypanosomal drug Eflornithine

113 ion, hypocotyl gravitropism, and chlorophyll biosynthesis, by physically interacting with PHYTOCHROME

114 genes include those associated with heptose biosynthesis, colonization, and stress resistance.

115 monstrate chemical inhibition of cholesterol biosynthesis compromises neurodevelopment.

116 but sugars, fatty acids and nucleotides for biosynthesis, conferring resistance to therapies targeti

117 andidate genes for straight-chain fatty acid biosynthesis confirmed their role in acylsugar metabolis

118 nzyme NadE catalyzes the last step of NAD(+) biosynthesis, converting nicotinic acid adenine dinucleo

119 xin transport, strigolactone and gibberellin biosynthesis, degradation of phospholipids and biosynthe

120 Plants harboring a mutation in DECREASE WAX BIOSYNTHESIS (DEWAX) are tolerant to UV-B.

121 Among them, inhibition of N-glycan biosynthesis enhanced Spike-protein proteolysis.

122 r fungal cell wall integrity, the hexosamine biosynthesis enzymes represent potential targets of anti

123 ved in bioluminescence, nonribosomal peptide biosynthesis, fatty acid activation, and beta-lactone fo

124 s in a branchpoint enzyme blocking quercetin biosynthesis, formed reduced numbers of lateral roots an

125 -defence pathway (opr7, aos1, 2, 3), terpene biosynthesis (fps3, tps2, 3, 4, 5, 7, 9, 10), benzoxazin

126 ched functional modules including tryptophan biosynthesis function.

127 and indicate that the penultimate step of GA biosynthesis, GA 20-oxidation, is required in both the m

128 oding variations of the brassinosteroid (BR) biosynthesis gene DWARF1 (DWF1) lead to variation of the

129 The conservation of geosmin biosynthesis genes among virtually all species of Strept

130 sors also show altered expression of hormone biosynthesis genes and aberrant growth patterns, includi

131 sion of GmNAC42-1, GmMYB29A1, and glyceollin biosynthesis genes and metabolites, respectively, in res

132 anscriptional coexpression network of lignin biosynthesis genes during secondary cell wall formation

133 ls was associated with priming of Pip and SA biosynthesis genes to induction by low levels of SA.

134 nthesis: a ribosomal RNA helicase gene, tRNA biosynthesis genes, and a gene controlling amino acid av

135 ogous genes for cutin formation, but not wax biosynthesis genes.

136 ial, including complex I and enzymes in Fe-S biosynthesis, grow relatively well at low oxygen and thu

137 However, biotin biosynthesis has been overlooked for priority pathogens

138 of Fe bioavailability, and increased NA/DMA biosynthesis has proved an effective Fe biofortification

139 etabolites that are funneled into polyketide biosynthesis has proven elusive.

140 mitochondrial protein involved in fatty acid biosynthesis, has now been identified as responsible for

141 Previous studies on MTL biosynthesis have suggested GDP-D-erythro-alpha-D-gluco-

142 r of cholesterol storage, uptake, efflux and biosynthesis, how these metabolic activities reprogram t

143 es enzymes for phosphatidylethanolamine (PE) biosynthesis; however, exogenous NBD-phosphatidylcholine

144 nto self-assembled networks during cellulose biosynthesis in a bacterial model, without altering the

145 apply PRISM 4 to chart secondary metabolite biosynthesis in a collection of over 10,000 bacterial ge

146 via an interaction with KCS1 to affect VLCFA biosynthesis in Arabidopsis.

147 nd 943 genes involved in the phenylpropanoid biosynthesis in leaf and root tissues respectively.

148 -dependent pathway is necessary for thiamine biosynthesis in Legionella pneumophila and provide bioch

149 CHS genes is likely associated with urushiol biosynthesis in mango.

150 The final step in mycolic acid biosynthesis in Mycobacterium tuberculosis is catalysed

151 H7PS), at the gateway to aromatic amino acid biosynthesis in Mycobacterium tuberculosis, which shows

152 demonstrate successful reconstruction of MbA biosynthesis in Nicotiana benthamiana.

153 identified here that could function in FuFA biosynthesis in other organisms.

154 tase enzyme FabI is essential for fatty acid biosynthesis in Staphylococcus aureus and represents a p

155 ghts the importance of NAMPT-mediated NAD(+) biosynthesis in the production of cisplatin-induced sene

156 Sites of GA biosynthesis in the roots of 7-d-old Arabidopsis thalian

157 Particularly, regulation of suberin biosynthesis in this group of plants remains poorly unde

158 tion of phenolic compounds, through phenolic biosynthesis, in acerola during postharvest storage.

159 iferation, immune responses, and cholesterol biosynthesis, increased infiltration of neutrophils, inf

160 l to uncover in vivo activity for the biotin biosynthesis inhibitor MAC13772.

161 ficiency and resistance to a toxic polyamine biosynthesis inhibitor methylglyoxal bis-(guanylhydrazon

162 Treatment with lovastatin, a mevalonate biosynthesis inhibitor, selectively inhibited protein pr

163 ctively dividing amastigotes from ergosterol biosynthesis inhibitors (azoles), independent of parasit

164 Cancers often escape the polyamine biosynthesis inhibitors by increased polyamine import.

165 e, and explains the failure of potent biotin biosynthesis inhibitors in standard mouse infection mode

166 Completion of coformycin biosynthesis involves reduction and dephosphorylation of

167 before mitochondrial matrix import for cPMP biosynthesis involving both proteins.

168 erculosis and Francisella tularensis, biotin biosynthesis is a key fitness determinant during infecti

169 ed in infected cells because host hexosamine biosynthesis is being exploited by the bacteria, in part

170 The first committed step in menaquinone biosynthesis is catalyzed by MenD, a thiamine diphosphat

171 n methods to explore Sec-facilitated protein biosynthesis is hindered by the large system sizes and l

172 cof gene cluster responsible for coformycin biosynthesis is identified.

173 However, the mechanism of its biosynthesis is incompletely understood.

174 However, the genetics of their biosynthesis is not fully understood, since no gene has

175 nt of the lower ligand in anaerobic cobamide biosynthesis is regiospecific.

176 A key step in bacteriochlorophyll biosynthesis is the reduction of protochlorophyllide to

177 PG biosynthesis is tightly coordinated with cell wall growt

178 shown to be involved in plant defense, their biosynthesis is unclear.

179 Ibuprofen, an inhibitor of prostanoid biosynthesis, is a common pharmacological agent used for

180 AD), which catalyzes the second step of heme biosynthesis, is an Fe-S protein.

181 a key component of mitochondrial fatty acid biosynthesis, is important in generating the fatty acid

182 candidate genes for a reaction in histidine biosynthesis lacking an annotated gene and highlight met

183 ailable datasets and tools, including glycan biosynthesis models, omics datasets, and systems-level a

184 ed cell proliferation, inflammation, steroid biosynthesis, neutrophils and macrophages infiltration,

185 alyzes the terminal chlorination step in the biosynthesis of (-)-acutumine.

186 of Streptomyces bacteria (and genes for the biosynthesis of 2-MIB in about 50%)(7,8), suggests that

187 we identify a CHS-L gene contributing to the biosynthesis of anthraquinones.

188 on of genes encoding enzymes involved in the biosynthesis of antimicrobial peptides, camalexin, and 4

189 ch catalyzes the first committed step in the biosynthesis of Asc.

190 ome analysis after biochemical inhibition of biosynthesis of branched-chain amino acids (precursors t

191 Stressed cells increase de novo biosynthesis of ceramides, which return to sub-toxic lev

192 f the prodrug pyrazinamide (PZA), interrupts biosynthesis of coenzyme A in Mycobacterium tuberculosis

193 This study demonstrates that the biosynthesis of complex fungal polyketides can be establ

194 ally occur as central building blocks in the biosynthesis of distinct monocot diterpenoids.

195 EC 2.1.1.28) catalyzes the final step in the biosynthesis of epinephrine and is a potential drug targ

196 aling module (KAI2-MAX2-SMAX1) regulates the biosynthesis of ethylene to fine-tune root and root hair

197 de experimental support for Jiang's proposed biosynthesis of exotine A and exotine B but also foresha

198 lular acetate and contributes to the de novo biosynthesis of fatty acids and Leu; peroxisome-localize

199 The biosynthesis of FeMo-co is performed stepwise and involv

200 olved in cystine/glutamate transport and the biosynthesis of glutathione, an antioxidant that may pro

201 osynthesis, degradation of phospholipids and biosynthesis of glycerolipid, downregulation of ammonium

202 Defects in the biosynthesis of GPI anchors in humans lead to inherited

203 The biosynthesis of hepatitis B virus (HBV) covalently close

204 refore may be excellent tools for commercial biosynthesis of important intermediates, final drug mole

205 hosphate synthase, an enzyme involved in the biosynthesis of l-Trp and indole acetic acid.

206 me-related organelles (LROs) is required for biosynthesis of most modular ascarosides as well as prev

207 arded as the main enzyme responsible for the biosynthesis of N-acylethanolamines (NAEs), a family of

208 so find that over-expressing BNA2, the first Biosynthesis of NAD(+) (kynurenine) pathway gene, reduce

209 m quinolinic acid, the precursor for de novo biosynthesis of nicotinamide adenine dinucleotide (NAD(+

210 These enzymes are frequently involved in the biosynthesis of nonproteinogenic amino acids as building

211 a large family of enzymes that catalyse the biosynthesis of oligosaccharides, polysaccharides, and g

212 rmation through two parallel pathways in the biosynthesis of paraherquamides A and G.

213 ns exist in extracts and are involved in the biosynthesis of PAs of plants.

214 f the shikimate pathway, is required for the biosynthesis of phenylalanine and tyrosine in bacteria,

215 the insertion of PlsX and thus regulates the biosynthesis of phospholipids in Gram-positive bacteria.

216 Here, we show that CAMTA123 also repress the biosynthesis of pipecolic acid (Pip) in healthy plants.

217 iched accumulation of proteins important for biosynthesis of plant defense secondary metabolites and

218 rbon into the TCA cycle, TGFbeta induced the biosynthesis of proline from glutamine in a Smad4-depend

219 S) machinery, expanding the paradigm for the biosynthesis of quinolone-gamma-lactam natural products

220 acid (SA)-mediated immunity, repressing the biosynthesis of SA in healthy plants.

221 ing a plausible explanation for the enhanced biosynthesis of secondary metabolism in the glandular tr

222 e their potential therapeutic relevance, the biosynthesis of serrulatane diterpenoids has not been pr

223 se compounds serve as key precursors for the biosynthesis of several important classes of plant natur

224 thase (MbtI) is a key enzyme involved in the biosynthesis of siderophores.

225 itoyltransferase (SPT) catalyses the de novo biosynthesis of sphingolipids but also produces noncanon

226 PHYB2-silenced plants, we demonstrated that biosynthesis of the major tomato fruit carotenoid, lycop

227 ynthetic biology experiments to decipher the biosynthesis of the monomethylated FuFA, methyl 9-(3-met

228 Biosynthesis of the NiFe(CN)(2)(CO) cofactor requires th

229 this study provides useful insight into the biosynthesis of the presilphiperfolanol natural products

230 origins and variation of genes governing the biosynthesis of these crucial phenotypic traits that hav

231 transfer protein (MTP), is required for the biosynthesis of these lipoproteins, and its regulation d

232 s mode of action, resistance mechanisms, and biosynthesis of this clinically important antimicrobial

233 nce factor (pvf) operon is essential for the biosynthesis of two very different natural product scaff

234 f these enzymes are required for cholesterol biosynthesis, only inhibition of the most upstream enzym

235 americana Our data showed that a block of JH biosynthesis or JH action arrested vitellogenesis, in pa

236 f the parasite, addressing the dependency on biosynthesis or salvage of fatty acids (FAs), purine nuc

237 Hexosamine biosynthesis pathway (HBP), a shunt pathway of glycolysi

238 ntiality makes this less explored mycobactin biosynthesis pathway a promising endogenous target for n

239 d in the emergence of a novel 2-ketobutyrate biosynthesis pathway based upon the promiscuous cleavage

240 nzymes responsible for most steps of the ABA biosynthesis pathway have been identified, enzymatic rea

241 RABIDOPSIS (TAA1), a key enzyme in the auxin biosynthesis pathway in Arabidopsis thaliana is phosphor

242 entify and evaluate regulators of the lignin biosynthesis pathway in Populus deltoides by combining g

243 suggesting that intermediates in the starch biosynthesis pathway increased flux through spillover pa

244 The lipopolysaccharide biosynthesis pathway is considered an attractive drug ta

245 This biosynthesis pathway is highly correlated with the activ

246 ermination of different intermediates in the biosynthesis pathway is of pivotal importance.

247 est that the upregulation of the cholesterol biosynthesis pathway may negatively impact fish growth d

248 onding primary breast tumors, use the serine biosynthesis pathway to support mTORC1 growth signaling.

249 The mycobactin biosynthesis pathway, conserved only among the mycolata

250 e (ADO), which function in a two-step alkane biosynthesis pathway.

251 ease expression of enzymes in the mevalonate biosynthesis pathway.

252 ty and its metabolism through the hexosamine biosynthesis pathway.

253 lator of the majority of genes in the lignin biosynthesis pathway.

254 as altered expression of genes in the lignin biosynthesis pathway.

255 scovery of biologically active anthraquinone biosynthesis pathways in medicinal plants.

256 Here, we summarize and compare bacterial biosynthesis pathways relying on the recognition and tra

257 f genes in the terpenoid backbone and sterol biosynthesis pathways upstream of pregnenolone synthesis

258 r factor kappa B (NF-kappaB) and cholesterol biosynthesis pathways were activated, and specific cytok

259 , we discuss the diversity in structure, the biosynthesis pathways, and the functions of bacteria-spe

260 t UM cells utilize glycolytic and nucleotide biosynthesis pathways, whereas OXPHOS(low) BAP1 mutant U

261 increase in cancer, immune, and cholesterol biosynthesis pathways.

262 nctionalities while providing information on biosynthesis, physiological context, and glycan fine str

263 ical, and chemical evidence that benzoxazole biosynthesis proceeds through an ester generated by an A

264 rough quantitative exploration of fatty acid biosynthesis processes for optimal biofuels, renewable f

265 By contrast, pGpp interacts with purine biosynthesis proteins but not with the GTPases.

266 ial roles in development, signaling, hormone biosynthesis, regulation of gene expression, stress resi

267 the 17q21 locus affecting ORMDL sphingolipid biosynthesis regulator 3 (ORMDL3) expression.

268 nd the stem tissue-specificity of paclitaxel biosynthesis-related enzymes remain largely unknown.

269 its tetrapyrrole biosynthesis and/or protein biosynthesis remains poorly understood.

270 Inhibition of isoprenoid biosynthesis repressed P(n) at high temperatures through

271 of a man-made explosive and in benzastatins biosynthesis, respectively, as very efficient C-H aminas

272 by inverting the order of nature's two-phase biosynthesis route.

273 mnat activities are essential for all NAD(+) biosynthesis routes, and understanding the regulation of

274 tes of the shikimate and aromatic amino acid biosynthesis (SA) pathways (upstream of BNA2), which pro

275 me distinct pathways such as heparan sulfate biosynthesis showed differences.

276 Pv03 dirigent-like gene, involved in lignin biosynthesis, showed a base-pair substitution that is as

277 regulatory programs, including phytohormone biosynthesis, signaling, and response, which were well c

278 and enzymes for the first four steps of MbA biosynthesis, starting from the flavonol precursor myric

279 Besides a role in cysteine biosynthesis, TgCBS can also efficiently produce hydroge

280 In tryptophan biosynthesis, the reaction catalyzed by the enzyme indol

281 rucial roles of adenylate-forming enzymes in biosynthesis, this also severely limits our ability to p

282 ed on strains with deficient or excessive PE biosynthesis to elucidate the mechanism.

283 We are exploring MbA biosynthesis to enable metabolic engineering of this rar

284 recycles one-carbon units lost to polyamine biosynthesis to the methionine cycle to overcome stress.

285 dentification of key genes involved in auxin biosynthesis, transport, and signaling.

286 ifferences in nucleotide salvage and de novo biosynthesis using a histologically heterogeneous breast

287 oll-like receptors via NF-kappaB, eicosanoid biosynthesis via the lipoxygenase pathway and IL-2 biosy

288 th clv2/crn signaling and heat-induced auxin biosynthesis via YUCCA family genes are synergistically

289 proach, and the role of TmMYB3 in paclitaxel biosynthesis was investigated.

290 that phosphocholine and phosphatidylcholine biosynthesis was markedly elevated in Traf3 (-/-) mouse

291 which tyrosine hydroxylase (TH), and thus DA biosynthesis, was conditionally ablated using either flo

292 (rbcL and RbcS), and enzymes of chlorophyll biosynthesis were down-regulated in the yellow leaf tiss

293 Glycolysis, FA and membrane lipid biosynthesis were repressed in GmLEC2a-OE but increased

294 e insensitive to a chemical inhibitor of Trp biosynthesis, which is a phenotype previously observed i

295 cent knowledge gained in the genetics of CHC biosynthesis, which is just beginning to incorporate wor

296 e confirmed that roots are autonomous for GA biosynthesis, which occurs in multiple tissues, with the

297 ochondrial redox generation promoted proline biosynthesis, while reducing mitochondrial redox potenti

298 P-glycosyltransferase, the first step in GPI biosynthesis, with good selectivity over the human funct

299 s are consistent with the early stages of GA biosynthesis within the root occurring in the meristemat

300 e Delta-14 reductase activity in cholesterol biosynthesis, yet little is known about their post-trans