ライフサイエンスコーパス: bioluminescent

1 ita surprisingly reveals that the species is bioluminescent.

2 of several triple fusion genes composed of a bioluminescent, a fluorescent, and a positron emission t

3 n be used to describe the synchronization of bioluminescent activity of abyssopelagic organisms with

4 ted in oral tumor development with increased bioluminescent activity within 6 days that reached a max

5 ction in size that still retains significant bioluminescent activity, in conjunction with a more repr

6 However, the bioluminescent and fluorescent components of fusion repo

7 ess lesser activities when compared with the bioluminescent and fluorescent components of the nonfusi

8 Reporter expression serves as detectable bioluminescent and fluorescent markers of VEEV and WEEV

9 CONCLUSIONS/SIGNIFICANCE: Bioluminescent and fluorescent optical imaging was combi

10 uction algorithm was used to co-register the bioluminescent and fluorescent signals with muCT images.

11 . chabaudi parasites expressing fluorescent, bioluminescent and model antigens that can be used in vi

12 Moreover, the proportion of bioluminescent and non-bioluminescent animals within tax

13 More than 97% of Cnidarians were bioluminescent, and 9 of the 13 taxonomic categories wer

14 The percentage of bioluminescent animals is remarkably uniform over depth.

15 er, the proportion of bioluminescent and non-bioluminescent animals within taxonomic groups changes w

16 These data indicate that a rapid bioluminescent antimicrobial susceptibility assay may be

17 Here we present a bioluminescent assay for the identification and characte

18 tive as compared to a commercially available bioluminescent assay in detecting mycoplasma contaminati

19 he detection of luciferase by implementing a bioluminescent assay in microfluidic reactors.

20 Other advantages of this bioluminescent assay over comparable fluorescent assays

21 2, 2C9, 2C19, 2D6 and 3A4) using an in vitro bioluminescent assay.

22 rs (called reactor II), were studied for the bioluminescent assay.

23 ened for endocrine disrupting activity using bioluminescent assays.

24 scribe the pathogenicity of three attenuated bioluminescent B. melitensis mutants, GR019 (virB4), GR0

25 eneral toxicity determination rely on either bioluminescent bacteria and specific medium solution (i.

26 The majority of bioluminescent bacteria localized in the cecum by 3 h po

27 We show that photons from bioluminescent bacteria radiate over mesoscopic distance

28 se progression of C57BL/6 mice infected with bioluminescent bacteria, imaged using optical tomography

29 ATP bioluminescent bacterial density quantitation was used t

30 Vibrio fischeri is a bioluminescent bacterium that enters into a symbiosis wi

31 The bioluminescent bacterium Vibrio fischeri initiates a spe

32 obal approach is now possible for the marine bioluminescent bacterium Vibrio fischeri, which exists e

33 between the squid Euprymna scolopes and the bioluminescent bacterium Vibrio fischeri.

34 The proposed hardware and software, called bioluminescent-based analyte quantitation by smartphone

35 6700) is a genetically engineered lux-based bioluminescent bioreporter.

36 As such, in vivo imaging of bioluminescent Borrelia provides a sensitive means to de

37 ructure of a generally low species diversity bioluminescent community at shallower epipelagic depths

38 Collectively, we show a winter bioluminescent community in the high Arctic with vertica

39 Additionally, the bioluminescent construct allowed for increased speed and

40 The bioluminescent constructs passed/exceeded pharmacopoeia-

41 ocument an association between the origin of bioluminescent courtship and increased accumulation of s

42 ishes, we find more species in lineages with bioluminescent courtship compared to their sister groups

43 e find under a Yule model that lineages with bioluminescent courtship displays have significantly hig

44 Here we show that lineages with bioluminescent courtship, almost certainly a sexually se

45 hat malignant cells expressing CXCR7 reduced bioluminescent CXCL12 secreted in the primary tumor micr

46 Capitalizing on sensitive detection of bioluminescent CXCL12, we also demonstrated that CXCR7+

47 However, correct interpretation of bioluminescent data is limited: the bioluminescence is d

48 n of E. coli K1 strain A192PP and a virulent bioluminescent derivative, E. coli A192PP-lux2.

49 The combination of sensitive ratiometric bioluminescent detection and the intrinsic modularity of

50 ecules enable highly sensitive and selective bioluminescent detection of FAAH activity in vitro, in l

51 , we describe a mouse model that enables the bioluminescent detection of GPCR activation in real time

52 assay for PI 4-kinase activity based on the bioluminescent detection of the ADP produced by kinase r

53 llans, a heterotrophic unarmored unicellular bioluminescent dinoflagellate, occurs widely in the ocea

54 of voltage-gated proton channels in 1972 in bioluminescent dinoflagellates, where they were thought

55 the 13 taxonomic categories were found to be bioluminescent dominant.

56 To expedite this method, we used bioluminescent E. coli in a simplified checkerboard assa

57 was also assessed in liquid cultures using a bioluminescent E. coli-O157:H7 strain.

58 Red-shifted bioluminescent emitters allow improved in vivo tissue pe

59 Furthermore, bioluminescent energy transfer assays indicated that whi

60 Using aqueous in situ polymerization on a bioluminescent enzyme anchored with polymerizable vinyl

61 y we examine the influence that locating the bioluminescent enzyme luciferase in different microcapsu

62 of microRNA, miR21 in cancer cells using the bioluminescent enzyme Renilla luciferase (Rluc) as a lab

63 terial kill curves constructed by exposing a bioluminescent Escherichia coli target, as a surrogate c

64 By multiplexing fluorescent and bioluminescent EV membrane reporters, we reveal the rapi

65 hese 'dark' V. fischeri strains remained non-bioluminescent even after treatment with both autoinduce

66 ET processes or use of initial chemical and bioluminescent excitation are treated similarly.

67 variants of Gluc, which maintain attractive bioluminescent features, and have characterized their sp

68 firefly species (Coleoptera: Lampyridae) use bioluminescent flashes for signaling.

69 ing glutamate stimulation, discrete Arc-Gluc bioluminescent flashes representing sites of de novo tra

70 lls from this donor mouse and image them for bioluminescent (fluc2), fluorescent (tdTomato), and posi

71 In vivo bioluminescent, fluorescent, X-ray and muCT imaging were

72 question, we developed a genetically encoded bioluminescent Forster resonance energy transfer (BRET)

73 nimals, we constructed and characterized the bioluminescent fusion reporters beta-cat firefly lucifer

74 ach, cargo (in this case, a fluorescent or a bioluminescent gene) is loaded onto the nanoparticles, w

75 Here we report development of the bioluminescent GSK3beta and CK1alpha reporter (BGCR) bas

76 Bioluminescent images of living mice, of excised whole i

77 Two days later, bioluminescent images were acquired in each mouse every

78 Bioluminescent imaging (BLI) is a widely used in vivo me

79 to study Plasmodium liver stages by means of bioluminescent imaging (BLI) of the rodent malaria paras

80 Bioluminescent imaging (BLI) of transplanted ASCs reveal

81 The other group was first screened by bioluminescent imaging (BLI) to select only mice with vi

82 Using bioluminescent imaging (BLI), we discovered that microsc

83 tor tumor angiogenesis and growth by in vivo bioluminescent imaging (BLI).

84 Using noninvasive bioluminescent imaging and a mathematical model of siRNA

85 Bioluminescent imaging and direct counts were used to fo

86 umor growth and metastasis were monitored by bioluminescent imaging and immunohistochemistry.

87 we evaluated the therapeutic efficacy using bioluminescent imaging and showed that the lung tumor gr

88 rates and localizations were confirmed using bioluminescent imaging and SPECT/CT after the (188)Re-BM

89 Bioluminescent imaging and tumor cell count showed a sig

90 In this study, we report that bioluminescent imaging can be reproducibly achieved with

91 . yoelii infection with sporozoites and that bioluminescent imaging can be used to monitor protective

92 The approach of bioluminescent imaging combined with mathematical modeli

93 Noninvasive bioluminescent imaging confirmed that DNase I treatment

94 Mice were then monitored with bioluminescent imaging for expression of both renilla (t

95 Furthermore, bioluminescent imaging in live mice to monitor macrophag

96 The GFAP signal, revealed by bioluminescent imaging in the living animal, was signifi

97 Bioluminescent imaging of encapsulated murine neonatal i

98 With a transgenic mouse line permitting the bioluminescent imaging of FAP(+) cells, we find that the

99 Bioluminescent imaging of ferrets infected with A/Califo

100 Thus, bioluminescent imaging of influenza infections rapidly d

101 Bioluminescent imaging of mice bearing luciferase-expres

102 Bioluminescent imaging of the reporter virus permits ser

103 In vivo bioluminescent imaging of these parasites allows for qua

104 Bioluminescent imaging of tumor metastases to the liver,

105 Bioluminescent imaging of vector-transduced mice demonst

106 In vivo bioluminescent imaging permits the visualization of bact

107 More strikingly, bioluminescent imaging revealed that dissemination of th

108 In vivo bioluminescent imaging showed that a GRA15-deficient typ

109 Bioluminescent imaging studies indicated that an optimiz

110 ics, estimated dosimetry, nano-SPECT/CT, and bioluminescent imaging suggest that the PEGylated liposo

111 ibronectin adhesin BBK32, were quantified by bioluminescent imaging to further evaluate their pathoge

112 Furthermore, using bioluminescent imaging to maximize data acquisition, we

113 PCa cells were shown by in vivo and ex vivo bioluminescent imaging to metastasize more rapidly and t

114 e use positron emission tomography (PET) and bioluminescent imaging to quantify the in vivo biodistri

115 To address this issue, we used in vivo bioluminescent imaging to track the fate of transplanted

116 Bioluminescent imaging was used to monitor encapsulated

117 ining humanized Renilla luciferase (hrl, for bioluminescent imaging), monomeric red fluorescence prot

118 asures included tumor growth, as measured by bioluminescent imaging, and median survival time.

119 ng virus in living mice can be visualized by bioluminescent imaging, bioluminescence being detected i

120 ence of phototoxicity, and photobleaching in bioluminescent imaging, combined with the ratiometric as

121 A combination of bioluminescent imaging, cultivation of infected tissues,

122 In the current studies, we used in vivo bioluminescent imaging, in vivo BrdU labeling, and three

123 Using quantitative bioluminescent imaging, we found that consecutive daily

124 Using bioluminescent imaging, we now demonstrate that H9 line

125 Using in vivo and ex vivo bioluminescent imaging, we observed that donor CD8(+) T

126 f patient-derived multiple myeloma cells and bioluminescent imaging, we were able to follow pMM cells

127 ESC engraftment was analyzed by bioluminescent imaging.

128 eralized loss of MCMV in brain, confirmed by bioluminescent imaging.

129 ed at 3, 5, 7, and 10 days post-treatment by bioluminescent imaging.

130 d protein inhibition measured by noninvasive bioluminescent imaging.

131 ion that can be detected noninvasively using bioluminescent imaging.

132 93T cells by both fluorescent microscopy and bioluminescent imaging.

133 gle-photon emission computed tomography, and bioluminescent imaging.

134 Since it is bioluminescent, imaging LOTUS-V does not require externa

135 Further, using a highly quantifiable bioluminescent in vivo model, drug combinations were at

136 o generate an optical signal (fluorescent or bioluminescent) in the presence of the target compound(s

137 development of the first genetically encoded bioluminescent indicator for membrane voltage called LOT

138 t fluorescent influenza B reporter virus and bioluminescent influenza B reporter virus.

139 ith transducing and transmitting traditional bioluminescent information.

140 table luminescence intensity occurred, graft bioluminescent intensity progressively decreased several

141 alaria, using the photoprotein aequorin as a bioluminescent label has been developed.

142 In that regard, the utilization of the bioluminescent label, Rluc, that offers the advantage of

143 and ease of use, fluorescent, enzymatic, and bioluminescent labels are often employed in such miniatu

144 the environment, such as a heat source or a bioluminescent life form, but we know little about how t

145 orescent proteins with the bright, glow-type bioluminescent light generated by an enhanced small luci

146 long-wavelength (from red to near-infrared) bioluminescent light in cells and in animals, even in de

147 This approach relies on the generation of bioluminescent light when two distinct cell populations

148 Analysis of bioluminescent live-cell imaging shows a significantly g

149 mel2, that displays similarity to bacterial bioluminescent loci and plays an important role during p

150 A wide variety of bioluminescent luciferase proteins are available for use

151 The bioluminescent marine bacterium Vibrio harveyi uses a ce

152 In the bioluminescent marine bacterium Vibrio harveyi, sensory

153 Vibrio fischeri, a bioluminescent marine bacterium, exists in an exclusive

154 The importance of bioluminescent marine taxa is highlighted in the water c

155 th different combinations of fluorescent and bioluminescent marker proteins and employing multi-modal

156 en different combinations of fluorescent and bioluminescent marker proteins and used bioluminescence

157 ion of FcgammaRs to this therapy model using bioluminescent measurement of lung metastases loads, nov

158 more, two-way ANOVA analysis showed that the bioluminescent method and traditional plate counting met

159 the traditional plate counting and the novel bioluminescent method for all bioluminescent strains.

160 The proteinase activity was analysed with a bioluminescent method using the light intensity decay co

161 all bioluminescent strains and therefore the bioluminescent method was accurate according to the crit

162 These strains demonstrated that the bioluminescent method was accurate, precise and equivale

163 Percentage recoveries using the bioluminescent method were between 70% and 130% for all

164 traditional plate counting method or the ATP bioluminescent method.

165 for the first time and applied as a label in bioluminescent microplate assay to detect target antibod

166 roup of Motyxia, the only genus of New World bioluminescent millipedes.

167 erase chain reaction and recently introduced bioluminescent miRNA detection, require systematic study

168 Using a new bioluminescent mouse model, we monitored p27 translation

169 he development of ATLL and HHM using a novel bioluminescent mouse model.

170 Infection of BALB/c mice with a bioluminescent mouse-adapted EV71 construct (mEV71-NLuc)

171 Stimulation of adoptively transferred bioluminescent MPhis and B-1a cells by amyloid fibrils r

172 ength, which extends the application of such bioluminescent nanocapsules, especially in deep tissue.

173 riety of luminescent--such as fluorescent or bioluminescent--objects.

174 Bioluminescent optical imaging and transcutaneous ultras

175 injected VEEV or WEEV, engineered to express bioluminescent or fluorescent reporters (fLUC and DsRed,

176 ression of imaging reporter genes for either bioluminescent or positron emission tomography (PET) ima

177 Bioluminescent organisms are likely to have an evolution

178 Among the least studied bioluminescent organisms are phylogenetically rare fungi

179 on of the entire transcriptomes in symbiotic bioluminescent organs (bacterial photophores) from two d

180 Here we show that bioluminescent organs of the squid Euprymna scolopes pos

181 ubstantially influence d-luciferin-dependent bioluminescent output in vivo.

182 nonhybrid natural fimbrolides as revealed by bioluminescent P. aeruginosa QS reporter assays and biof

183 In vivo imaging of bioluminescent parasites has previously been shown to be

184 In this review, fluorescent and bioluminescent PCAs are discussed and their application

185 The reporter phage conferred a bioluminescent phenotype to Y. pestis within 12 min of i

186 all, this study demonstrates that the use of bioluminescent primary ALL allows the detection and quan

187 Caged Luciferin-1 (PCL-1), a chemoselective bioluminescent probe for the real-time detection of H(2)

188 A substantial advantage of beta-gal as a bioluminescent probe is that the enzyme retains full act

189 ization of iron-caged luciferin-1 (ICL-1), a bioluminescent probe that enables longitudinal monitorin

190 Bioluminescent probes with emission in near-infrared (NI

191 Model simulations show that predicted bioluminescent profiles can be very different from chang

192 - and green-emitting luciferase mutants with bioluminescent properties suitable for dual-color report

193 of fluorescent ligands in combination with a bioluminescent protein (NanoLuc) that can be readily exp

194 e-presenting quantum dots to a mutant of the bioluminescent protein Renilla reniformis luciferase.

195 put (564-nm peak wavelength) of any reported bioluminescent protein that utilizes its natural substra

196 s article reviews the most pertinent current bioluminescent-protein-based technologies and suggests t

197 Bioluminescent proteins are used in a plethora of analyt

198 These nanosensors consist of bioluminescent proteins as the BRET donor, quantum dots

199 While the use of bioluminescent proteins for molecular imaging is a power

200 perates with biochemical energy generated by bioluminescent proteins to excite fluorophores and offer

201 dyes, luminescent lanthanide complexes, and bioluminescent proteins.

202 ep tissues than firefly luciferase and other bioluminescent proteins.

203 x5/2 scaling result experimentally using the bioluminescent reaction between ATP and luciferase/lucif

204 with protein microcrystals that catalyse the bioluminescent reaction using ATP and the substrate coel

205 action to release d-luciferin for subsequent bioluminescent reaction with firefly luciferase.

206 uded microfluidics, ATP measurements using a bioluminescent reaction, and rheology.

207 Bioluminescent recording of circadian clock protein (PER

208 Furthermore, cryogels impregnated with bioluminescent reporter cells provided enhanced survival

209 he triple fusion vector carrying mtfl as the bioluminescent reporter component showed significantly (

210 Firefly luciferase (FLuc), an ATP-dependent bioluminescent reporter enzyme, is broadly used in chemi

211 tions of Copper-Caged Luciferin-1 (CCL-1), a bioluminescent reporter for tissue-specific copper visua

212 Bioluminescent reporter genes are sensitive in situ tool

213 ificity of the promoter, which regulates the bioluminescent reporter genes, limits the metal detectio

214 chnologies rely on the use of fluorescent or bioluminescent reporter genes, which need to be stably e

215 led Antares, functions as a highly sensitive bioluminescent reporter in vivo, producing substantially

216 were used to evaluate luminescence from the bioluminescent reporter Pseudomonas fluorescens M3A.

217 Thus, a robust bioluminescent reporter strategy enabled rigorous quanti

218 Using a kappaB(5)-->IkappaBalpha-FLuc bioluminescent reporter, we rigorously evaluated the dyn

219 we monitored the replication and spread of a bioluminescent reporter-expressing NiV in susceptible mi

220 The ultrasensitive detection limits of bioluminescent reporters are especially advantageous whe

221 However, bioluminescent reporters currently do not have the multi

222 Secreted luciferases are highly useful bioluminescent reporters for cell-based assays and drug

223 Bioluminescent reporters were employed to detect active

224 s thus pave the way to an extended family of bioluminescent reporters.

225 By using radioligand binding and bioluminescent resonance energy transfer (BRET) assays i

226 previously shown that a genetically encoded bioluminescent resonance energy transfer (BRET) biosenso

227 teraction of P2Y12 with PAR4 but not PAR1 by bioluminescent resonance energy transfer when the recept

228 Using bioluminescent resonance energy transfer-2, we showed th

229 etent 293T transfectants when assessed using bioluminescent resonance energy transfer.

230 Using bioluminescent resonant energy transfer, we have demonst

231 release firefly luciferin, which triggers a bioluminescent response in the presence of firefly lucif

232 ts on the backs of mice were infected with a bioluminescent S. aureus (methicillin sensitive) or USA3

233 possess EGFP-fluorescent neutrophils, and a bioluminescent S. aureus strain (Xen29; 1x10(3) CFUs) wa

234 likely to cause reflections), and under the bioluminescent searchlights of potential predators, anim

235 Here, a bioluminescent sensor is developed for non-invasively an

236 A new study finds that the evolution of bioluminescent sexual displays drives high species richn

237 Here, we found evidence that bioluminescent sharks instead emit a constant light outp

238 A novel luciferin from a bioluminescent Siberian earthworm Fridericia heliota was

239 firefly luciferin in situ, giving rise to a bioluminescent signal if and only if both chemical trigg

240 Tomographic reconstruction of the bioluminescent signal in mice expressing luciferase only

241 adjacent organs and observing a predominant bioluminescent signal in the pancreas compared with live

242 he fused fluorophore generates the brightest bioluminescent signal known to date, including improved

243 The bioluminescent signal measured for these mice on Day 4 p

244 tis by rapidly and specifically conferring a bioluminescent signal response to these cells.

245 ure culture and human serum by transducing a bioluminescent signal response.

246 ion of Ca(2+) solution and discriminated via bioluminescent signal spectral and time resolution.

247 nally verified by the ability to transduce a bioluminescent signal to recipient cells.

248 ter phage, E. coli O157:H7 produces a strong bioluminescent signal upon addition of commercial lucife

249 nal design providing a 1000-fold increase in bioluminescent signal upon addition of the TEV protease.

250 Peak background subtracted bioluminescent signal was fourfold higher when cells wer

251 extGLuc+ cells emitted significantly higher bioluminescent signal when compared to cells expressing

252 n vivo, mouse extGLuc+ T cells showed higher bioluminescent signal when compared to GLuc+ and RLuc+ T

253 tituent strongly affects the strength of the bioluminescent signal, which varies widely based on size

254 or did it significantly quench the resulting bioluminescent signal.

255 nd a Beta-Glo assay system for generation of bioluminescent signal.

256 ting photophores were partially co-opted for bioluminescent signalling, leading to complex patterns.

257 extrapancreatic tissues, we did not observe bioluminescent signals from extrapancreatic tissues of d

258 of 5FC resulted in significant inhibition of bioluminescent signals in mice whose tumors had been inf

259 The bacterial bioluminescent signals of the S. aureus-infected mice pe

260 rin in most neurons generated large and fast bioluminescent signals that were related to neural activ

261 d a progressive increase in their pancreatic bioluminescent signals, which were positively correlated

262 and the possibilities of detecting low-level bioluminescent signals.

263 ilities was confirmed by the delivery of the bioluminescent small molecule probe luciferin and turnov

264 ruggle to perceive dim downwelling light and bioluminescent sources and the need to remain unseen gen

265 phy, and PET), tomographic reconstruction of bioluminescent sources, and two unique, complementary mo

266 were infected by intranasal instillation of bioluminescent strain 536 and received 536_P1 intranasal

267 ns of bradyzoite-specific SRSs, we created a bioluminescent strain lacking the expression of SRS9, on

268 We created a bioluminescent strain of S. epidermidis and developed a

269 ent method were between 70% and 130% for all bioluminescent strains and therefore the bioluminescent

270 he hypothesis that these newly described non-bioluminescent strains exhibit monophyly within the V. f

271 omonas aeruginosa ATCC9027 and its validated bioluminescent strains for preservative efficacy tests u

272 ation was evaluated against lawn biofilms of bioluminescent strains of Staphylococcus aureus and Pseu

273 Bioluminescent strains of the Arabidopsis thaliana patho

274 characterization of naturally occurring, non-bioluminescent strains of Vibrio fischeri.

275 plicability of five constitutively-expressed bioluminescent strains was evaluated for preservative ef

276 Validation of the bioluminescent strains was performed in accordance with

277 ed a competitive disadvantage against native bioluminescent strains when colonizing the light organ o

278 Pseudomonas aeruginosa and Escherichia coli bioluminescent strains, we studied the combination of L-

279 and the novel bioluminescent method for all bioluminescent strains.

280 O activity in human plasma samples using the bioluminescent substrate L-012.

281 6'-alkylated aminoluciferins are shown to be bioluminescent substrates for Ultra-Glo and QuantiLum lu

282 n of the ponyfish supports the growth of the bioluminescent symbiont Photobacterium leiognathi.

283 he squid Euprymna scolopes and its specific, bioluminescent symbiont, Vibrio fischeri.

284 A few enigmatic bioluminescent symbionts have not been successfully cult

285 The majority of bacteria engaged in bioluminescent symbiosis are environmentally acquired an

286 Finally, four other rarely studied bioluminescent systems (those of limpet Latia, earthworm

287 The origins and functions of some bioluminescent systems, however, remain obscure.

288 We developed a new approach to bioluminescent T cell imaging using a membrane-anchored

289 eventh the volume), slower growing, and less bioluminescent than P-form cells; they are also avirulen

290 , is an important simple model for efficient bioluminescent transformations.

291 inducer of apoptosis (TWEAK), we developed a bioluminescent variant of soluble TWEAK (GpL-FLAG-TNC-TW

292 oreover, intravenous administrated PSES-TSTA bioluminescent vector correctly identified tibial bone m

293 experimentally evolved ecologically distinct bioluminescent Vibrio fischeri by colonization and growt

294 t colonization of Euprymna scolopes squid by bioluminescent Vibrio fischeri from the North Pacific Oc

295 cyl carrier protein synthetase (AasS) of the bioluminescent Vibrio harveyi strain B392 has been isola

296 026 (BMEI1090-BMEI1091), and the dynamics of bioluminescent virulent bacterial infection following va

297 e subsequently challenged on day 24 with the bioluminescent WT CO92 strain (20 to 28 LD50s), 40 to 70

298 trans-tibial implant that was precoated with bioluminescent Xen36 S. aureus.

299 5I-Bcr-Abl without appreciable toxicity in a bioluminescent xenograft mouse model using a transformed

300 report the development and optimization of a bioluminescent yeast assay for the detection of organoti