ライフサイエンスコーパス: mutant strain

1 dent growth of the M. smegmatis tam deletion mutant strain.

2 e domain, is sufficient to complement a rocA mutant strain.

3 uted to an altered membrane potential in the mutant strain.

4 the DeltawcaM DeltacsgA DeltayihO DeltabcsE mutant strain.

5 ated iron acquisition is impaired in an sbnI mutant strain.

6 gnificantly upregulated in the fabT deletion mutant strain.

7 h a newly characterized curved-rod Delta1228 mutant strain.

8 sistant to oxidants than a catalase-deletion mutant strain.

9 type M59 GAS, we constructed an isogenic mga mutant strain.

10 failed to support growth of an E. coli acpP mutant strain.

11 x II failed to support growth of the E. coli mutant strain.

12 pts of intron-spliced isoforms in the MoHMT1 mutant strain.

13 perature-sensitive phenotype of an spo7Delta mutant strain.

14 but at a substantially lower level in a CMD1 mutant strain.

15 ut were undetectable in the pigmentless snf2 mutant strain.

16 enes were significantly reduced in the dkppx mutant strain.

17 se activity was altered in the yjbH and yjbI mutant strains.

18 f Deltainv, DeltayadA, and DeltainvDeltayadA mutant strains.

19 xposed to H pylori, including cagPAI and cgt mutant strains.

20 sequences in both wild type and degradosome mutant strains.

21 ainst the wild type virus and drug-resistant mutant strains.

22 did not lead to the development of resistant mutant strains.

23 lated RNA ends in ribonuclease wild-type and mutant strains.

24 and cellular phenotypes of the wild-type and mutant strains.

25 in both the E. coli parent and aceE deletion mutant strains.

26 d A isolated from the corresponding deletion mutant strains.

27 eading to the recovery of covR, covS or rocA mutant strains.

28 Hsp70 biology has emerged from studying ssa mutant strains.

29 eron, by developing knock-out and functional mutant strains.

30 specific antibodies via the emergence of new mutant strains.

31 compared to single Deltagra12 or Deltarop18 mutant strains.

32 tical to those of the corresponding deletion mutant strains.

33 iter, with little effect on nearly identical mutant strains.

34 microcolonies between the EmaA positive and mutant strains.

35 species: a collection of genetically related mutant strains.

36 genetic interactions in single and multiple mutant strains, (2) can identify drug targets, (3) detec

37 Using an E. coli mutant (strain 536DeltafyuA) unable to acquire yersiniab

38 Notably, most mutant strains accumulate wild-type cellular levels of t

39 This mutant strain accumulates abnormally high levels of puri

40 A DeltaeseJ mutant strain adheres to epithelioma papillosum of carp

41 Chemical analyses of generated mutant strains allowed for the identification of a trike

42 terized straight-rod Deltapgp1 and Deltapgp2 mutant strains, along with a newly characterized curved-

43 The mutant strains also produced very reduced amounts of eth

44 t (Saccharomyces cerevisiae) SEIPIN deletion mutant strain and a plant (Nicotiana benthamiana) transi

45 ry aspergillosis since a sulfate transporter mutant strain and a sulfite reductase mutant strain are

46 We then constructed these novel mutant strains and compared their observed phenotypes to

47 e are increased in both fast and slow Pol II mutant strains and the magnitude of half-life changes co

48 urement of the relative fitness of bacterial mutants, strains and species in mixed inocula in the hos

49 orphisms (n = 48), an isogenic rocA deletion mutant strain, and five isogenic rocA polymorphism mutan

50 different inoculation techniques, bacterial mutant strains, and assays for the hypersensitive respon

51 ences were examined in the single and double mutant strains, and the virulence of select strains was

52 oot architectures, including wildtype and 10 mutant strains, and we uncovered a design principle that

53 troso-guanidine mutagenesis and selection, a mutant strain Apmu4 was derived, in which the rate of lo

54 Akinetes in the mutant strain appeared normal, but these cultures were l

55 porter mutant strain and a sulfite reductase mutant strain are fully virulent.

56 The guide sequences, editing constructs, and mutant strains are freely available to researchers to in

57 oli communities can be established where the mutant strains are metabolically coupled.

58 sulfate was about 3-4x as great in the A666G mutant strain as in the wild type.

59 rocessing of 16S rRNA is also delayed in the mutant strain, as indicated by increased levels of precu

60 Even fecal-recovery numbers for both mutant strains at several time points prior to the anima

61 onsistent with these observations, the H273D mutant strain attenuated GAS virulence, whereas the H273

62 at the espACD regulatory region of the phoP mutant strain because of PhoP-EspR protein-protein inter

63 expression decreased in the CN3718 codY-null mutant strain but significantly increased in the SM101 c

64 proteins was not negatively affected in the mutant strains, but still the capacity for nonphotochemi

65 V. cholerae mutant strains carrying inactivated AI synthase genes we

66 ed to the wild-type strain, a H201R isogenic mutant strain caused significantly larger skin lesions i

67 cytogenes infection, a reduced number of the mutant strain compared to the parental strain was observ

68 f infection with the wild-type strain or the mutant strain complemented with lipA ROS derived from th

69 ESR was partially induced in the siw14Delta mutant strain, consistent with the increased stress resi

70 All madC mutant strains contain loss-of-function point mutations

71 gas was detected in a hydrogenase quadruple-mutant strain containing deletions in the hya, hyb, hyd,

72 created and examined a DeltacopAZ DeltacopBL mutant strain (cop-).

73 ity level, we asked whether matrix-defective mutant strains could be coaxed to produce functional mat

74 r cell signaling, and the germination of rpf mutant strains could not be stimulated by the addition o

75 Here we generate a new deletion mutant strain, CVS-N2c(DeltaG), and examine its neuronal

76 ingae pv tomato DC3000 and the nonpathogenic mutant strain DC3000hrpA- allowed us to establish causal

77 Experiments with a T. dentrificans mutant strain defective in U(IV) oxidation supported mic

78 Finally, the mtsR mutant strains defective in metal sensing and oligomeriz

79 riptional profiling of roots inoculated with mutant strains defective in the synthesis of Nod Factor

80 Mutant strains, defective in sRNAs or in ARGONAUTE3 (a k

81 activity is higher in 33277, and an isogenic mutant strain deficient for the gingipains exhibited an

82 In contrast, both wild-type and mutant strains deficient for peroxiredoxins and glutathi

83 erexpression of COY1 inhibited the growth of mutant strains deficient in fusion activity at the Golgi

84 n flux ranges and the presence or absence of mutant strains delivering flux towards pathways of inter

85 A MakatG1 deletion mutant strain (DeltaMakatG1) showed decreased catalase a

86 Escherichia coli, or Pseudomonas aeruginosa mutant strain DeltapopB Moreover, BMDMs deficient in IRF

87 riptional profiles were compared between the mutant strain DeltarelA [a (p)ppGpp(0) strain under gluc

88 rgeted gene deletion confirmed that isogenic mutant strains DeltaspyAD and Deltaisp2 are significantl

89 A B. pseudomallei DeltappiB (BpsDeltappiB) mutant strain demonstrates impaired biofilm formation an

90 gnificantly increased in the SM101 codY-null mutant strain, demonstrating CodY-dependent regulation d

91 er, we found that a slowly constricting fzlA mutant strain develops 'pointy' poles, suggesting that F

92 uring growth in vitro However, the DeltaphtY mutant strain did not display an increased CP sensitivit

93 Despite high expression of ACT, the rseA mutant strain did not infect the murine airway as effici

94 The DeltaohyA mutant strain did not recover from the 16:1(9Z) challeng

95 This bacterial mutant strain did not stimulate colitis in dnKO mice.

96 as the DeltaadcA, DeltaadcAII, and DeltaphtD mutant strains displayed less CP sensitivity during grow

97 the general fitness of the amoebae with the mutant strain displaying a substantial growth defect.

98 Importantly, the DeltaeseJ mutant strain does not replicate efficiently in EPC cell

99 etween M. tuberculosis H37Rv and a DeltanarL mutant strain during exponential growth in broth culture

100 wild-type, rocA mutant, covS mutant and covR mutant strains during invasive infection and their fitne

101 g. 1-phenyl-2-thiourea, PTU) or pigmentation mutant strains (e.g. casper mutant).

102 Individual DeltatrxA and DeltatrxC deletion mutant strains each show a greater abundance of lipid pe

103 he hypothesis that vaccination with the batA mutant strain elicits protective immunity against subseq

104 We generated a Drosophila Adar(E374A) mutant strain encoding a catalytically inactive Adar wit

105 ed defects in Mia40 oxidation, only one erv1 mutant strain (erv1-1) had significantly decreased activ

106 murine model of aspergillosis, the Deltagna1 mutant strain exhibited attenuated virulence.

107 Despite gaining phage resistance, epa mutant strains exhibited a loss of resistance to cell wa

108 t H273 and H327 relieved inhibition, and the mutant strains exhibited a wild-type phenotype.

109 In contrast to cen9Delta mutants, cen10Delta mutant strains exhibited growth defects and were aneuplo

110 We showed that the rRV mutant strains exhibited impaired viral replication and

111 Each of the Walker box mutant strains exhibited properties identical to those o

112 n original strategy that combined the use of mutant strains expressing catalytically inactive variant

113 strain expressing both HMW1 and HMW2 and the mutant strains expressing either HMW1 or HMW2 were able

114 We analyse 230 signature-tagged mutant strains for 114 putative phosphatases under 30 di

115 A screen with S. pombe transcription factor mutant strains for growth sensitivity to the AEO fractio

116 To further elucidate regulatory controls, mutant strains for histidine kinases PhoR and AioS were

117 We consistently found that mutant strains for RNAi (dcr1Delta, ago1Delta, rdp1Delta

118 ld-type strain and an isogenic fabT deletion mutant strain found that between 3.7 and 28.5% of the S.

119 1;3 and OsPIP2;6 were displayed in yeast HD9 mutant strain (fps1acr3ycf1) as a result of increased B

120 ysis shows that the transmission rate of the mutant strain from mosquitoes to human is more influenti

121 representative isolates and "leaky melanin" mutant strains from each species complex to examine the

122 An exogenous EL mimic protected mutant strains from hNP-1 and hBD-2 but not RP-1, indica

123 on techniques can be used to distinguish FKS mutant strains from wild type, but testing C. glabrata w

124 ith the increased stress resistance, and the mutant strain further induced the ESR in response to oxi

125 g mutant mice, we characterized Rhbdf1 mouse mutant strains generated by three commonly used strategi

126 The mutant strain grew normally under iron-limiting conditio

127 nt, hopper(Bd-we), isolated from a white eye mutant strain had an intact transposase reading frame an

128 orescent reporter proteins revealed that the mutant strain had greatly enlarged peroxisomes up to 10

129 virulence characteristics, and the quadruple-mutant strain had the same (greatly attenuated) phenotyp

130 The DeltacsrA mutant strains had a greatly reduced ability to kill Gal

131 The DeltacsrA mutant strains had a reduced ability to survive drying a

132 Mutant strains harbouring transposon insertions in two s

133 release, and an ato5Delta ATO1(G53D) double mutant strain has additive alkalinization and ammonia re

134 Y181C, Y188L, IRLL98, and K103N+Y181C HIV-1 mutant strains, highlighting the importance of the alpha

135 V. cholerae and a locked low-cell-density QS-mutant strain identified 7,240 transcriptional start sit

136 Whole genome sequencing of the wild-type and mutant strains identified a point mutation that creates

137 oci analysis, machine learning, and isogenic mutant strains identified and confirmed a one-nucleotide

138 ollowed by genome sequencing of the isolated mutant strains identified mutations that disrupt DNA dam

139 In all mutant strains, impaired maturation of white matter astr

140 The virulence of the mutant strain in a murine model of melioidosis demonstra

141 w that Cu strongly inhibits growth of a copA mutant strain in acidic cultures.

142 experiments with a PEP carboxylase-deficient mutant strain in blood and cerebrospinal fluid.

143 CMV infection resolution and emergence of a mutant strain in high-risk recipients of kidney transpla

144 t mortality between wild-type and DSB repair mutant strains in any model of infection.

145 re limited data on disease manifestations of mutant strains in children.

146 were necessary for fitness in lasR+ and lasR mutant strains in colony biofilms grown in microoxic con

147 forming growth curves with WT, alsT and gltS mutant strains in defined medium supplemented with ammon

148 roteome changes of wild type UA159 and lrgAB mutant strains in response to these same stresses.

149 Surprisingly, when mutant strains in the genes involved in virulence (JDelt

150 Indeed, evolving 7 PF mutant strains in the presence of drug revealed 3 adapta

151 lker-B) in each of the ATPases and generated mutant strains in which these motifs were altered.

152 length maintenance by utilizing yku70-R456E mutant strains, in which Ku has reduced DEB and telomere

153 Using a novel P. gingivalis W50 PPAD mutant strain, incapable of protein citrullination, and

154 vironments, to characterization of different mutant strains, including those harbouring synthetic cir

155 ested by the hypersensitivity of a Deltasod1 mutant strain, increased resistance afforded by the supe

156 n and metabolism were all accelerated in the mutant strain indicative of dysregulated oxidative phosp

157 We show that this mutant strain is able to metabolise xylose to acetate on

158 in mouse lung 24 h post infection while the mutant strain is cleared by host defense mechanisms.

159 Finally, we show that an E. faecalis epa mutant strain is deficient in intestinal colonization, c

160 Congruous with ex vivo findings, a nfu mutant strain is more susceptible to oxidative killing b

161 munity afforded by vaccination with the batA mutant strain is predominantly mediated by IgG antibodie

162 Two Helicobacter mutant strains (katA(H56A) and katA(Y339A)) containing c

163 abelled LA did not differ between the WT and mutant strains, LA induced more cell membrane damage in

164 The mutant strain lacking both SPN and SLO production is sev

165 to colonize more frequently than the double mutant strain lacking HMW1 and HMW2.

166 tion model and that HA levels increased in a mutant strain lacking hyaluronidase (HysA).

167 by Pseudomonas aeruginosa wild-type versus a mutant strain lacking multiple porins.

168 ia and soft tissue infection models, and the mutant strain lacking production of both toxins is furth

169 in several nitrogen sources, we found that a mutant strain lacking the Mycobacterium proteasomal acti

170 An S. Typhimurium mutant strain lacking these two effectors exhibits marke

171 Mutant strains lacking Cagalpha, Cagbeta, or CagE (putat

172 Furthermore, 33277 and 381 mutant strains lacking CTD cell surface proteins were mo

173 iffusion in wild-type V. cholerae to that in mutant strains lacking either toxR or the toxT promoter,

174 Here, isogenic mutant strains lacking EmaA structures, but still expres

175 We show that mutant strains lacking gigC have impaired growth in the

176 s lysozyme resistance of L. monocytogenes as mutant strains lacking gpsB showed an increased lysozyme

177 Experiments with mutant strains lacking mitochondrial superoxide dismutas

178 Mutant strains lacking mneP are Mn(II) sensitive and acc

179 Mutant strains lacking the spermine synthase-encoding ge

180 Similarly to a carR mutant, strains lacking almE, almF, and almG exhibited e

181 Like a ume6 mutant, strains lacking SAP6 exhibit enhanced colonizati

182 Mongolian gerbils with an H. pylori pgdA(-) mutant strain led to significantly decreased levels of i

183 on of LipA from Xac306 and verified that the mutant strain lost most of its lipase and esterase activ

184 We found that a mutant strain (mac1Delta) lacking Mac1, a copper-sensing

185 Two other mutant strains made truncated versions of the protein.

186 quire a live, stable, lipid-rich E. gracilis mutant strain, named B1ZFeL, with 40% more lipid content

187 clude the generation of large collections of mutant strains, now available for forward- and reverse-g

188 An ibeA deletion mutant strain (NRG857cDeltaibeA) was constructed, and th

189 A mutant strain of C. neoformans that cannot transport xyl

190 the reference strain and homozygous deletion mutant strain of CCC2, which encodes a Cu(2+)-transporti

191 compared to a DeltarelADeltaspoT (ppGpp(0)) mutant strain of E. coli, deficient in the stringent res

192 We also determine that the high-persister mutant strain of Escherichia coli, HipQ, is associated w

193 A mutant strain of L. monocytogenes expressing the cystein

194 ROS inhibitor) or LGGOmegaSpaC (an adhesion-mutant strain of LGG) or FPR1-knockout mice.

195 tient 103 (PA103) supernatant] or defective [mutant strain of P. aeruginosa lacking a functional type

196 e, where symptoms are reduced in a Deltaexl1 mutant strain of P. atrosepticum.

197 easure the mechanical properties of T4P of a mutant strain of Pseudomonas aeruginosa PAO1 unable to r

198 tpatient LRTI because of a newly circulating mutant strain of RSV B.

199 1) from S. atroolivacues SB3033, a DeltalnmE mutant strain of S. atroolivaceus S-140.

200 because killed bacteria and a protease-null mutant strain of S. aureus were unable to penetrate.

201 c-psbA4 gene from Cyanothece 51142 in a 4E-3 mutant strain of the model non-nitrogen-fixing cyanobact

202 We use a dynactin mutant strain of the multinucleate fungus Ashbya gossypi

203 A colonization-deficient mutant strain of this intracellular bacterium is able to

204 Bs2 gene since no effect was observed when a mutant strain of Xcc with a disruption in avrBs2 gene wa

205 much faster "colony surfing" still occurs in mutant strains of Bacillus subtilis lacking flagella.

206 -producing and a noninvasive hypha-producing mutant strains of C. albicans.

207 xperimental data for different wild type and mutant strains of C. botulinum Group I type A1.

208 of photoautotrophically grown wild-type and mutant strains of Chlamydomonas reinhardtii to determine

209 option of choice to check both wild-type and mutant strains of different origins.

210 ease progression using Caenorhaditis elegans mutant strains of dnj-14, the worm orthologue of DNAJC5.

211 irus (IAV) infection including wild-type and mutant strains of H1N1 and H3N2 subtypes.

212 mic has been exacerbated by the emergence of mutant strains of Mtb that are resistant to frontline an

213 oughput sequencing (Hi-C) with wild-type and mutant strains of Neurospora crassa to gain insight into

214 al lesions, both capsular-defective knockout mutant strains of P. gingivalis induced less alveolar bo

215 Isogenic mutant strains of S. aureus with varying degree (Deltare

216 Surprisingly, mutant strains of S. mutans with impairment in RGP side

217 Here we show that mutant strains of S. praecaptivus that lack genetic comp

218 Furthermore, mutant strains of T. forsythia, devoid of either mirolys

219 Using mutant strains of these bacteria that are defective in t

220 to a toxic concentration of toluene, a tolR mutant strain or a strain overexpressing a diguanylate c

221 Using a pde2 mutant strain, pApA was detected for the first time in S

222 On plants, the Deltanmo2 mutant strain penetrated host cuticles like wild type, b

223 tii nopA::Tn or a Dot/Icm-defective dotA::Tn mutant strain present a functional innate immune respons

224 transformants of a somatic regenerator (Reg) mutant strain receiving sgRNA plasmid with glsA protospa

225 during the growth of the wild-type and sigL mutant strains reduced expression of the toxin genes, in

226 that the majority of cells in a Deltasll1130 mutant strain remained unicellular and viable after prol

227 produce an mif(-/-) strain of L. major This mutant strain replicated normally in vitro but had a 2-f

228 SMG-free, quadruple vic mutant strains representing both allelic backgrounds of

229 n situ reconstitution of fnm in the deletion mutant strain restored adherence.

230 Our analyses of wild-type and mutant strains reveal key elements of chromosome archite

231 ic Cu(+) Analysis of DeltacopR and DeltacueR mutant strains revealed a CopR regulon composed of genes

232 scriptome analysis of the wild-type and dcl3 mutant strains revealed a further difference from higher

233 Phenotypic analysis of the mutant strains revealed that disruption of icsA abolishe

234 DeltadevR, DeltadevSDeltadosT, and DeltanarL mutant strains revealed that in response to nitrite prod

235 nal carbon; the core oscillator in the prd-1 mutant strain runs with a long period under glucose-suff

236 itch variability is heritable, and comparing mutant strains selectively bred to high and low penetran

237 ated MRSA parental and their respective sarA mutant strain sets.

238 Unexpectedly, the mutant strain showed increased serum resistance.

239 Goats infected with the mutant strain showed only transient fever.

240 tion in the wild type and an IsoMO-disrupted mutant strain showed that epoxyisoprene, or a subsequent

241 for correct fungal development as the AaGPx3 mutant strains showed a severe reduction in conidiation.

242 EM of the compensatory mutant strains showed complete virus particles, but thes

243 s and biological confirmation with different mutant strains showed that this life extension is due to

244 FACT in deubiquitinating H2B in vivo, a FACT mutant strain shows elevated levels of H2B-Ub.

245 tion frequency, particularly in an ung1Delta mutant strain, suggesting that dCas9 induces mutations t

246 aexlx-gh5 rescued the movement defect of the mutant strain, suggesting that expansin and GH5 function

247 transcripts that were more abundant in dcl3 mutant strains than in wild-type cells were not due to s

248 C (11G5 strain) isolated from a patient or a mutant strain that does not produce colibactin (11G5Delt

249 we describe the genome engineering of a RF1 mutant strain that enhances suppression efficiency durin

250 enetically engineered centrin gene knock-out mutant strain that is antibiotic resistant marker free a

251 Specifically, we generated a mutant strain that lacks all 13 PTS transporters, and fr

252 Mutant strains that are dsbA or dsbB null facilitate lab

253 ding increasing concentrations of sulfate to mutant strains that are unable to incorporate H2S effici

254 combine phenotypic and genotypic analyses of mutant strains that suggest discrepancies in the literat

255 In the two mutant strains, the flexural rigidity is not significant

256 colonized with R. gnavus wild-type (WT) and mutant strains-the fitness of the nan mutant was signifi

257 ully restored the wild-type phenotype of the mutant strain; this indicates that P55 plays no importan

258 still substantially impact the phenotypes of mutant strains through epistasis.

259 or screening mutants and establishing stable mutant strains through genetic crosses.

260 of Chlamydomonas reinhardtii and the use of mutant strains to analyze photosynthesis was conducted i

261 The varied sensitivity of the mutant strains to CP-mediated Zn limitation suggests dis

262 notation of new genes, and the generation of mutant strains to define the role of genes in complex en

263 strain, and five isogenic rocA polymorphism mutant strains to perform genome-wide transcript analysi

264 Here, we utilize P. gingivalis mutant strains to show that pathogen-differentiated mDCs

265 Mutant strains tolerant to levels of aromatic acids near

266 satisfies fluxomic data for wild-type and 25 mutant strains under different substrates and growth con

267 The capsule mutant strain was also impaired for survival in guinea p

268 tbreak data in North-Eastern Italy where the mutant strain was detected.

269 5 transporters confirmed that each isogenic mutant strain was significantly (P < 0.05) impaired in c

270 The B. abortus bab1_1517 mutant strain was significantly attenuated in macrophage

271 ii, we observed that the growth of DeltacsrA mutant strains was inhibited in the presence of amino ac

272 xpression by epithelial cells exposed to psm mutant strains was significantly increased compared to t

273 Using isogenic mutant strains, we demonstrate that deleting one or more

274 Using isoallelic mutant strains, we found that 3 polymorphisms in this to

275 Using FGDelta-mutant strains, we showed that specific combinations of

276 S(0) globules from a Chlorobaculum tepidum mutant strain were purified and used to show that the wi

277 The mutant strains were examined for CPS quantity, size, and

278 Two mutant strains were generated: one where expression of t

279 We also observed that the mutant strains were more sensitive than WT cells to high

280 Whereas DeltaagrB mutant strains were not able to produce biofilms, a Delt

281 differences in MICs between WT and DeltaTolC mutant strains were not reflected by equal differences i

282 ptation, exocytosis, and endocytosis in sec3 mutant strains were similarly alleviated by mutation of

283 The DeltaadcC and DeltarpsN.2 mutant strains were the most susceptible to CP, whereas

284 d Pseudomonas putida G7 Y1, a nonchemotactic mutant strain, were simultaneously introduced into the s

285 ExaF reduces methanol sensitivity in the fae mutant strain when lanthanides are present, providing ev

286 egulated by RpoE, and surprisingly, the rseA mutant strain where RpoE activity was elevated expressed

287 Capsule production is abolished in the mutant strain, which is concomitant with its inability t

288 a consistent failure of C. reinhardtii vtc1 mutant strains, which are deficient in polyphosphate syn

289 Using a mutant strain with a high differentiation rate and fluor

290 rbidity and mortality, particularly if a CMV mutant strain with antiviral resistance emerges.

291 nserted into the C. besciigenome, creating a mutant strain with its S-layer extensively decorated wit

292 ion with either wild-type cryptococci or the mutant strain with reduced surface xylose; although iBAL

293 Complementation of the mutant strain with the wild-type SNF2 gene restored pigm

294 sporter mediated this increase, we generated mutant strains with a deletion of SPE1 or SPE2 combined

295 generate and phenotypically characterize 29 mutant strains with deletions of individual transporter

296 Mutant strains with disrupted RGP synthesis failed to pr

297 hpA The expression of uhpT was absent in the mutant strains with uhpT deletion and was not inducible

298 ing molecular mass in both the wild-type and mutant strains with various subsets of phenylalanine-gly

299 One (+/0) mutant strain, with multiple mutations at the mating loc

300 whereas in the csr-1 partially rescued null mutant strain (WM193), this mark is ectopically deposite