ライフサイエンスコーパス: ATCC

1 ATCC and clinical strains of Acanthamoeba that failed to

2 ce of the type strain Moritella marina MP-1 (ATCC 15381), having 4,636,778 bp with a G+C content of 4

3 We designate the type strain NSH-16 (= ATCC BAA-2463 = NCTC 13792).

4 says and human colon adenocarcinoma (Caco-2, ATCC, Rockville, MD) and human larynx carcinoma (HEp-2,

5 ille, MD) and human larynx carcinoma (HEp-2, ATCC, Rockville, MD) cells were used for bacterial adhes

6 re placed with S aureus strains: ATCC 25923, ATCC 29213, and K9328H.

7 poBC, dnaK, and hsp65 were amplified from 29 ATCC reference strains and 17 clinical isolates and sequ

8 mutase, in human macrophages infected with 3 ATCC and 5 clinical isolates of L.V. guyanensis, and L.V

9 Thermoanaerobacter pseudethanolicus 39E (ATCC 33223), a thermophilic, Fe(III)-reducing, and ferme

10 In the QC study, 4 of the 6 ATCC strains showed interlaboratory agreement of >90%.

11 Rat intestinal epithelial cells (IEC-6, ATCC, Rockville, MD) were used for proliferation, migrat

12 Using a database grounded by 60 ATCC reference strains, a total of 394 clinical fungal i

13 ene in the type strain of genomic species 9 (ATCC 9957) relative to the gene in the type strain of A.

14 from Streptoalloteichus hindustanus E465-94 ATCC 31158, that the tlmK gene is responsible for the at

15 Based on the M. abscessus ATCC 19977(T) genome, regions that discriminated between

16 E fermentations of the WT C. acetobutylicum (ATCC 824), as well as its mutants, using data obtained f

17 lytic activity of Lactobacillus acidophilus (ATCC(R) 4356), Lactobacillus casei (ATCC(R) 393) and Lac

18 ms, as revealed by studies on P. aeroginosa (ATCC 25619).

19 able bacterial killing against P. aeruginosa ATCC 27853 and no nephrotoxicity was found after systemi

20 .015 to 0.06 mug/ml), Pseudomonas aeruginosa ATCC 27853 (0.5 to 2 mug/ml and 17 to 23 mm), Escherichi

21 ady been developed in Pseudomonas aeruginosa ATCC 9027.

22 Unlike F. alocis ATCC 35896, the D-62D strain expressed more proteins dur

23 two Bacillus cereus strains (ATCC 10987 and ATCC 14579) have been sequenced.

24 re glycans in Bacillus cereus ATCC 14579 and ATCC 10876.

25 rent strains of F. nucleatum; ATCC 25586 and ATCC 23726 induce significantly more hBD-2 mRNA than ATC

26 ed control strains: S. aureus ATCC 29213 and ATCC 25923, Escherichia coli ATCC 25922, Haemophilus inf

27 icrog, while Bacillus cereus strains 569 and ATCC 10987 were transformed with efficiencies of 10(4) a

28 evolutionary intermediate between Hall A and ATCC 3502.

29 of CM-05 and 004-737X (which lack cfr), and ATCC 29213 (an LNZ-susceptible control).

30 nome sequence of the type strain O. anthropi ATCC 49188, which revealed the presence of two chromosom

31 C58 and Oant2987 from Ochrobactrum anthropi ATCC 49188 were found to catalyze the hydrolysis of acet

32 0.015 mug/ml and 28 to 35 mm), and S. aureus ATCC 25923 (32 to 38 mm).

33 nd 23 to 30 mm, respectively), and S. aureus ATCC 25923 (disk diffusion zone diameter range, 18 to 26

34 e determined to be 25 to 31 mm for S. aureus ATCC 25923, 25 to 31 mm for S. pneumoniae ATCC 49619, an

35 lar activity against Gram-positive S. aureus ATCC 25923.

36 cus aureus ATCC 25923 (disk only), S. aureus ATCC 29213 (broth only), Enterococcus faecalis ATCC 2921

37 nges for selected control strains: S. aureus ATCC 29213 and ATCC 25923, Escherichia coli ATCC 25922,

38 ined to be 0.06 to 0.25 mug/ml for S. aureus ATCC 29213, 0.016 to 0.12 mug/ml for E. faecalis ATCC 29

39 thromycin were tested: Staphylococcus aureus ATCC 25923 (disk only), S. aureus ATCC 29213 (broth only

40 s for control strains: Staphylococcus aureus ATCC 29213 (0.004 to 0.015 mug/ml), Enterococcus faecali

41 ns (updated MIC range) Staphylococcus aureus ATCC 29213 (0.03 to 0.12 mug/ml), Enterococcus faecalis

42 QC ranges for strains Staphylococcus aureus ATCC 29213 (MIC range, 1 to 4 mug/ml), Haemophilus influ

43 Staphylococcus aureus ATCC 29213 and 25923, Streptococcus pneumoniae ATCC 4961

44 acteria, in particular Staphylococcus aureus ATCC 6538, Listeria monocytogenes ATCC 13932 and methici

45 depend on the expression of the A. baumannii ATCC 17978 A1S_2225 gene, which codes for an 18.6-kDa pr

46 Ata were highly opsonic against A. baumannii ATCC 17978 and showed low to moderate killing activity a

47 ificantly reduced the levels of A. baumannii ATCC 17978 and two MDR strains in the lungs of infected

48 ificantly enhanced virulence of A. baumannii ATCC 17978 cells cultured in the presence of ethanol whe

49 sure increases the virulence of A. baumannii ATCC 17978.

50 er, these results indicate that A. baumannii ATCC 19606(T) produces three independent TonB proteins,

51 transposon insertion library of A. baumannii ATCC 19606T resulted in the identification of the 2010 d

52 although the C terminus of the A. baumannii ATCC 19606T SecA is not essential for viability, it play

53 am-negative pathogen Acinetobacter baumannii ATCC 17961 (MIC = 0.0078 muM).

54 In comparison, Bifidobacterium breve ATCC 15700 showed significantly less HMO catabolic activ

55 we uncover two genes in Lactobacillus brevis ATCC 367, tstT and tstR, encoding for a rhodanese and a

56 de (V.harveyi ATTC BAA-1116 and V.campbellii ATCC 25920).

57 CCUG 48324(T), 97.9% similarity to S. canis ATCC 43496(T), and 97.8% similarity to S. ictaluri ATCC

58 cluster has been characterized from S. canus ATCC 12646: it spans approximately 80.5 kb and consists

59 cin analogues produced by Streptomyces canus ATCC 12646 were identified.

60 erance response (ATR) in Lactobacillus casei ATCC 334.

61 he amount of immobilized Lactobacillus casei ATCC 393 on wheat grains on the generation of volatile c

62 ure (free or immobilized Lactobacillus casei ATCC 393 on wheat grains) and the ripening time on the g

63 ophilus (ATCC(R) 4356), Lactobacillus casei (ATCC(R) 393) and Lactobacillus paracasei subsp. paracase

64 A. castellanii (ATCC 50370), A. polyphaga (ATCC 30461), and A. hatchetti

65 Here, we show two genes in B. cereus ATCC 14579 encoding enzymes involved in the synthesis of

66 We have demonstrated that B. cereus ATCC 14579 takes up (55)Fe radiolabeled ferric citrate a

67 e identified a four-gene operon in B. cereus ATCC 14579 that encodes proteins with the following sequ

68 a beta-mercaptoethanol extract of B. cereus ATCC 4342 spores.

69 ens, Vibrio breoganii 1C-10, Bacillus cereus ATCC 10987, Campylobacter jejuni subsp. jejuni 81-176 an

70 e linked to spore glycans in Bacillus cereus ATCC 14579 and ATCC 10876.

71 Thiocillins from Bacillus cereus ATCC 14579 are members of the well-known thiazolyl pepti

72 The thiocillins from Bacillus cereus ATCC 14579 are natural products from the broader class o

73 Bacillus cereus ATCC 14579 converts the C-terminal 14 residues of a 52-m

74 m thiocillin biosynthesis in Bacillus cereus ATCC 14579.

75 chlorophenol by Sphingobium chlorophenolicum ATCC 39723.

76 The genome sequence of S. clavuligerus ATCC 27064 was examined for a potential biosynthetic gen

77 molar activity against Gram-negative E. coli ATCC 25922 in colony counting assays, the wild-type disu

78 i 381 and the reference human strain E. coli ATCC 25922 was completed with Illumina HiSeq.

79 m inhibitory concentration (MIC) for E. coli ATCC 25922, and both sulphated PEPS and sulphated ST1275

80 ays employing enterobactin-deficient E. coli ATCC 33475 (ent-) revealed that six conjugates based on

81 the field, the number of culturable E. coli ATCC 700728 was reduced by up to 1000-fold, whereas PCR-

82 2 mug/ml and 17 to 23 mm), Escherichia coli ATCC 25922 (0.008 to 0.03 mug/ml and 30 to 36 mm), Haemo

83 antibacterial properties on Escherichia coli ATCC 25922 and Listeria innocua HPB 13.

84 est inhibition zone against Escherichia coli ATCC 25922 and Staphylococcus aureus CMCC 26003 while su

85 ATCC 29213 and ATCC 25923, Escherichia coli ATCC 25922, Haemophilus influenzae ATCC 49247, and Strep

86 chloride on the growth inhibition of E.coli (ATCC strain 33876) caused by Ag toxicity.

87 f 80 mg/mL against a model Escherichia coli (ATCC 25922).

88 othece sp. American Type Culture Collection (ATCC) 51142 is capable of performing oxygenic photosynth

89 ilar to an American Type Culture Collection (ATCC) strain of P. aeruginosa on ERIC-PCR.

90 responding American Type Culture Collection (ATCC) type strains, 47 other microbial species, and huma

91 ry strain (American Type Culture Collection [ATCC] 25586) or a clinical strain (Anaerobe Helsinki Neg

92 level of degradation of insulation concerned ATCC 25923.

93 CR assays was specific for the corresponding ATCC type strain serovar.

94 = 24) were orally infected with T. denticola ATCC 35404 and were euthanized after 12 and 24 weeks.

95 The encapsulated ATCC 15305 strain was resistant to complement-mediated o

96 urium ATCC 14028, Staphylococcus epidermidis ATCC 12228, Enterococcus faecalis ATCC 29212, and Escher

97 29213, 0.016 to 0.12 mug/ml for E. faecalis ATCC 29212, 0.008 to 0.03 mug/ml for S. pneumoniae ATCC

98 .004 to 0.015 mug/ml), Enterococcus faecalis ATCC 29212 (0.015 to 0.06 mug/ml), Pseudomonas aeruginos

99 (0.03 to 0.12 mug/ml), Enterococcus faecalis ATCC 29212 (0.03 to 0.12 mug/ml), and Streptococcus pneu

100 CC 29213 (broth only), Enterococcus faecalis ATCC 29212 (broth only), Streptococcus pneumoniae ATCC 4

101 Enterococcus faecalis ATCC 29212, a vancomycin-sensitive strain, has been exte

102 pidermidis ATCC 12228, Enterococcus faecalis ATCC 29212, and Escherichia coli DH5alpha, onto two mode

103 domonas putida KT2440, Enterococcus faecalis ATCC 29212, Salmonella Typhimurium ATCC 14028, and Esche

104 close relative of Streptomyces flavogriseus ATCC 33331.

105 pergillus fumigatus ATCC MYA-3626, A. flavus ATCC MYA-3631, A. terreus ATCC MYA-3633, and Fusarium ve

106 putida NCIB 9816 and Pseudomonas fluorescens ATCC 17483 containing naphthalene dioxygenases was assoc

107 Biofilm of Fn ATCC 25586 or AHN 9508 were produced by culturing each s

108 ated iron acquisition system is critical for ATCC 19606(T) to establish an infection and kill this ve

109 ng immunogen PS A1 from Bacteroides fragilis ATCC 25285/NCTC 9343 via a physiologically stable oxime

110 DCK-2), and mouse myoblast (C2C12) (all from ATCC, Manassas, VA).

111 ot, however, STR markers did not differ from ATCC reference for any sample.

112 and posaconazole (33 to 43 mm); A. fumigatus ATCC MYA-3626, amphotericin B (18 to 25 mm), itraconazol

113 ariotii ATCC MYA-3630, Aspergillus fumigatus ATCC MYA-3626, A. flavus ATCC MYA-3631, A. terreus ATCC

114 1), a probiotic (Lactobacillus rhamnosus GG, ATCC 53103), or placebo (microcrystalline cellulose) bet

115 Both P. gingivalis ATCC 33277 and an isogenic DeltaSerB mutant colonized th

116 fective mutant (FLL451) in the P. gingivalis ATCC 33277 genetic background showed a phenotype similar

117 We report here that P. gingivalis ATCC 33277 is remarkable in its ability to interact with

118 stablished and inoculated with P. gingivalis ATCC 33277 or YPF1, a major fimbriae-deficient mutant of

119 In a dpp4-7-11-disrupted P. gingivalis ATCC 33277, a DPP7-like activity still remained.

120 ral recognized as safe) strain C. glutamicum ATCC 13032 (CgNal).

121 y, we show that the mucin-degrader R. gnavus ATCC 29149 strain produces an intramolecular trans-siali

122 Furthermore, binding of R. gnavus ATCC 29149 to intestinal mucus is sialic acid mediated.

123 y control (QC) ranges for the N. gonorrhoeae ATCC 49226 control strain for MIC agar dilution testing

124 of the fdm cluster from Streptomyces griseus ATCC 43944, however, failed to reveal genes encoding the

125 previously cloned from Streptomyces griseus ATCC 49344 and successfully expressed in the heterologou

126 la pneumophila serogroup 12 strain 570-CO-H (ATCC 43290), a clinical isolate from the Colorado Depart

127 olygalacturonase from Streptomyces halstedii ATCC 10897.

128 uality draft genome sequence for G. hansenii ATCC 53582 and find that in addition to the previously d

129 s aiming to genetically engineer G. hansenii ATCC 53582 for increased cellulose productivity.

130 Gluconacetobacter hansenii ATCC 53582 is one of the highest reported bacterial cell

131 3496(T), and 97.8% similarity to S. ictaluri ATCC BAA-1300(T).

132 ly fully functional entB ortholog present in ATCC 19606(T).

133 The sequence in ATCC 19977T was designated sequevar (type) 1; most macro

134 tronic copy; all are actively transcribed in ATCC 19606(T).

135 solates with MICs of >/=16 mug/ml, including ATCC 19977T, revealed 10 sequevars.

136 riptomes of B. bifidum SC555 and B. infantis ATCC 15697 showed that utilization of pooled HMO is simi

137 se in Bifidobacterium longum subsp. infantis ATCC 15697 (B. infantis).

138 TCC 49619, and 16 to 20 mm for H. influenzae ATCC 49247.

139 C 49619, and 2 to 8 mug/ml for H. influenzae ATCC 49247.

140 /ml and 30 to 36 mm), Haemophilus influenzae ATCC 49247 (0.002 to 0.015 mug/ml and 31 to 39 mm), Stre

141 (disk and broth), and Haemophilus influenzae ATCC 49247 (disk and broth).

142 ange, 1 to 4 mug/ml), Haemophilus influenzae ATCC 49247 (MIC and disk diffusion zone diameter ranges,

143 chia coli ATCC 25922, Haemophilus influenzae ATCC 49247, and Streptococcus pneumoniae ATCC 49619.

144 oniae ATCC 49619, and Haemophilus influenzae ATCC 4927 strains were evaluated.

145 t in toxin (Rtx) of an environmental isolate ATCC 7966 of Aeromonas hydrophila consists of six genes

146 i_pse, in Bacillus thuringiensis israelensis ATCC 35646, which encodes seven different enzymes that t

147 CdiIYkris complex from Yersinia kristensenii ATCC 33638.

148 niliforme] ATCC MYA-3629) and Candida krusei ATCC 6258 by the CLSI disk diffusion method (M51-A docum

149 and 10208C; all P <0.05) but not laboratory (ATCC 33277, W83) P. gingivalis strains.

150 ions were excluded), were randomized to LGG (ATCC 53103) or placebo, once daily for 4 weeks.

151 o the gene in the type strain of A. lwoffii (ATCC 15309).

152 d NRRL 3882 and Streptomyces lysosuperificus ATCC 31396.

153 in (MDP) is produced by Actinomadura madurae ATCC 39144.

154 tionally derived information about B. mallei ATCC 23344 and literature-based and computationally deri

155 ore, we assessed the role of QS in B. mallei ATCC 23344 by constructing and characterizing a mutant s

156 ot analyses demonstrated that when B. mallei ATCC 23344 was complemented in trans with oacA, it synth

157 inst lethal aerosol challenge with B. mallei ATCC 23344, it also protects against infection with mult

158 cally similar to those produced by B. mallei ATCC 23344.

159 model using the virulent Burkholderia mallei ATCC 23344 strain.

160 . rubrum ATCC MYA-4438 and T. mentagrophytes ATCC 28185 were selected as QC isolates, with an accepta

161 ted 6 blinded T. rubrum or T. mentagrophytes ATCC strains.

162 , and Fusarium verticillioides [moniliforme] ATCC MYA-3629) and Candida krusei ATCC 6258 by the CLSI

163 cus aureus ATCC 6538, Listeria monocytogenes ATCC 13932 and methicillin-resistant S. aureus clinical

164 s of B. cenocepacia J2315 and B. multivorans ATCC 17616 in parallel (designated iPY1537 and iJB1411,

165 15, B. cenocepacia K56-2, and B. multivorans ATCC 17616 on 104 carbon sources.

166 ans UA159, as well as Actinomyces naeslundii ATCC 12104 and Streptococcus oralis ATCC 9811, grown on

167 Nine ATCC strains of Acanthamoeba and 40 delinked, biobanked,

168 N. nova ATCC BAA-2227 is proposed as a quality control organism

169 Recently, we demonstrated that F. nucleatum ATCC 23726 coaggregates with C. albicans SN152, a proces

170 We found that F. nucleatum ATCC 23726 inhibits growth and hyphal morphogenesis of C

171 ve FAD-I (nFAD-I) isolated from F. nucleatum ATCC 25586.

172 eatum strains of subspecies (ssp.) nucleatum ATCC 25586, ssp. polymorphum ATCC 10953, and ssp. vincen

173 ion and characterization of an F. nucleatum (ATCC 25586)-associated defensin inducer (FAD-I).

174 hBD-2 by different strains of F. nucleatum; ATCC 25586 and ATCC 23726 induce significantly more hBD-

175 nctions significantly reduces the ability of ATCC 19606(T) cells to persist and kill this host, a def

176 Mutagenesis analysis of ATCC 19606(T) tonB1 (subscripted numbers represent diffe

177 oth suspensions and spiked blood cultures of ATCC strains and clinical isolates with select gram-nega

178 cture with three small gaps in the genome of ATCC 19397 and one additional gap in the genome of Hall

179 -2-inducing strains in a DeltafadI mutant of ATCC 10953 resulted in hBD-2 induction to levels compara

180 However, the RtxA of ATCC 7966, as well as from the clinical isolate SSU of A

181 mid backbones suitable for transformation of ATCC 53582, albeit with low efficiencies.

182 viously described cellulose synthase operon, ATCC 53582 contains two additional cellulose synthase op

183 eslundii ATCC 12104 and Streptococcus oralis ATCC 9811, grown on machine-etched glass slides to gener

184 lization locus (PUL) from Bacteroides ovatus ATCC 8483 is transcriptionally up-regulated during growt

185 nd Lactobacillus paracasei subsp. paracasei (ATCC(R) BAA52) in yogurt.

186 (LIG group) or by oral gavage (GAV) with Pg ATCC 33277.

187 spectra acquired on Francisella philomiragia ATCC 25015 and on Francisella tularensis subsp. tularens

188 ed using a synbiotic containing L. plantarum ATCC-202195.

189 the reference strain Lactobacillus plantarum ATCC 14917, was chosen for further analysis.

190 us ATCC 25923, 25 to 31 mm for S. pneumoniae ATCC 49619, and 16 to 20 mm for H. influenzae ATCC 49247

191 9212, 0.008 to 0.03 mug/ml for S. pneumoniae ATCC 49619, and 2 to 8 mug/ml for H. influenzae ATCC 492

192 l and 31 to 39 mm), Streptococcus pneumoniae ATCC 49619 (0.004 to 0.015 mug/ml and 28 to 35 mm), and

193 o 0.12 mug/ml), and Streptococcus pneumoniae ATCC 49619 (0.004 to 0.015 mug/ml).

194 29212 (broth only), Streptococcus pneumoniae ATCC 49619 (disk and broth), and Haemophilus influenzae

195 mm, respectively), Streptococcus pneumoniae ATCC 49619 (MIC and disk diffusion zone diameter ranges,

196 CC 29213 and 25923, Streptococcus pneumoniae ATCC 49619, and Haemophilus influenzae ATCC 4927 strains

197 zae ATCC 49247, and Streptococcus pneumoniae ATCC 49619.

198 ssp.) nucleatum ATCC 25586, ssp. polymorphum ATCC 10953, and ssp. vincentii ATCC 49256.

199 A. castellanii (ATCC 50370), A. polyphaga (ATCC 30461), and A. hatchetti (CDC: V573) were adapted t

200 Nostoc punctiforme ATCC 29133 is a filamentous cyanobacterium that expresse

201 s from the cyanobacterium Nostoc punctiforme ATCC 29133, we establish that this spectral diversity ca

202 sis by the cyanobacterium Nostoc punctiforme ATCC 29133.

203 sis in the cyanobacterium Nostoc punctiforme ATCC 29133; we now report on the expression response of

204 In contrast, the reference ATCC isolate was unable to cause infection.

205 e we describe the draft genome of L. reuteri ATCC 53608, isolated from a pig.

206 ion was further confirmed using a L. reuteri ATCC PTA 6475 lar_0958 KO mutant (6475-KO).

207 richia coli JM109, and Lactobacillus reuteri ATCC PTA 4659.

208 determine if probiotic Lactobacillus reuteri ATCC PTA 6475 is effective in suppressing disease sympto

209 lactic acid bacterium Lactobacillus reuteri ATCC PTA 6475.

210 n liquid stillage by Lactobacillus rhamnosus ATCC 7469 was studied.

211 T. rubrum ATCC MYA-4438 and T. mentagrophytes ATCC 28185 were sele

212 from the original frozen vials from the same ATCC lot, however, STR markers did not differ from ATCC

213 S. saprophyticus ATCC 15305 CP, visualized by immunoelectron microscopy,

214 Agrobacterium sp. ATCC 31749 is an industrial strain for the commercial pr

215 ic and microoxic processes of Cyanothece sp. ATCC 51142 under continuous high irradiance and in high

216 Cyanothece sp. ATCC 51142, a member of this genus, has been shown to pe

217 Here, we describe Cyanothece sp. ATCC 51142, a unicellular, diazotrophic cyanobacterium w

218 cyanobacterial cells, such as Cyanothece sp. ATCC 51142, are capable of nitrogen fixation, a highly o

219 te light-driven metabolism in Cyanothece sp. ATCC 51142, with a particular focus on reductant product

220 diazotrophic cyanobacterium, Cyanothece sp. ATCC 51142.

221 a unicellular cyanobacterium, Cyanothece sp. ATCC 51142.

222 a, such as the enterobacterium, Serratia sp. ATCC 39006 (S39006).

223 In Serratia sp. ATCC 39006 and the plant pathogen Erwinia carotovora ssp

224 ution crystal structure for the Serratia sp. ATCC 39006 carbapenem resistance protein CarG.

225 um Erwinia (Pectobacterium) and Serratia sp. ATCC 39006, intrinsic resistance to the carbapenem antib

226 Strain ATCC 19606(T) utilizes the siderophore acinetobactin to

227 Strain ATCC 25791 (originally submitted as an example of Mycoba

228 ospholipase class A1 autotransporter (strain ATCC 25586, gene FN1704) that we hereby rename Fusobacte

229 ith 1 x 10(9) P. gingivalis bacteria (strain ATCC 33277).

230 plete genome sequence of F. columnare strain ATCC 49512.

231 UMGNA_01855 from Ruminococcus gnavus (strain ATCC 29149) [PDB:4HYZ] have been solved by X-ray crystal

232 In Escherichia coli O157:H7 strain ATCC 43895, a guanine-to-thymine transversion in the csg

233 s of the nontoxigenic E. coli O157:H7 strain ATCC 700728 and the virulent strain EC4045 declined 100

234 In strain ATCC 700819 (a.k.a. NCTC 11168), the modified heptose br

235 logy, we inactivated the tcsR gene in strain ATCC 9714.

236 ntrols and in F. nucleatum laboratory strain ATCC cocultures throughout the epithelium, in contrast t

237 y derived information about B. mallei strain ATCC 23344.

238 ave determined the genome sequence of strain ATCC 23769.

239 st complete genome of F. philomiragia strain ATCC 25017, which was isolated as a free-living microorg

240 Previously, strain ATCC 19606 was the only A. baumannii strain demonstrated

241 ome sequence of the curdlan-producing strain ATCC 31749.

242 protein, PatN, in Nostoc punctiforme strain ATCC 29133 leads to a threefold increase in heterocyst f

243 .3 to 8.3%, relative to the reference strain ATCC 19977(T).

244 S. saprophyticus strain ATCC 15305 capD, capL, and capK (capD(Ssp), capL(Ssp), a

245 S. saprophyticus strain ATCC 15305 carries two staphylococcal cassette chromosom

246 Serratia sp. strain ATCC 39006 produces the red-pigmented antibiotic prodigi

247 chnology and showed strong binding to strain ATCC 19606.

248 utation in the batA gene of wild-type strain ATCC 23344 was found to be particularly attenuating, as

249 level distinguishing it from the type strain ATCC 27405.

250 toxin production by C. difficile type strain ATCC 9689 under 768 culture conditions.

251 e produced by Streptomyces venezuelae strain ATCC 15439.

252 ared to vehicle-treated mice, whereas strain ATCC PTA 6475 increased cell migration (2-fold) without

253 The M. tuberculosis H37Rv strain (ATCC 25618) was used as the reference strain.

254 SA1679a and the reference human MRSA strain (ATCC 29213) was performed using Illumina-based transcrip

255 ollowing challenge with A. baumannii strains ATCC 19606 and clinical isolates (CI) 77, 78, 79, 80, an

256 The genomes of two Bacillus cereus strains (ATCC 10987 and ATCC 14579) have been sequenced.

257 fragments were placed with S aureus strains: ATCC 25923, ATCC 29213, and K9328H.

258 thiazolyl peptide GE37468 from Streptomyces ATCC 55365 and its heterologous expression in the model

259 demonstrated using living Bacillus subtilis ATCC 49760 colonies on agar plates.

260 subtilin producing strain Bacillus subtilis ATCC 6633.

261 SA-13 on spores formed by Bacillus subtilis (ATCC 6051), we performed the series of experiments confi

262 onal gap in the genome of Hall A, suggesting ATCC 19379 as an evolutionary intermediate between Hall

263 compared to the parent polymyxin-susceptible ATCC 19606.

264 gap-free genome assembly for M. sympodialis (ATCC 42132), comprising eight nuclear and one mitochondr

265 from Pseudoalteromonas carrageenovora 9(T) (ATCC 43555(T)).

266 Hydrocarboniphaga effusa strain AP103(T) (ATCC BAA-332(T)) is a member of the Gammaproteobacteria

267 Caldicellulosiruptor obsidiansis OB47(T) (ATCC BAA-2073, JCM 16842) is an extremely thermophilic,

268 YA-3626, A. flavus ATCC MYA-3631, A. terreus ATCC MYA-3633, and Fusarium verticillioides [moniliforme

269 Raoultella terrigena ATCC 33257 produces an O-antigen possessing the same dis

270 oniae serotype O12 (and Raoultella terrigena ATCC 33257).

271 26 induce significantly more hBD-2 mRNA than ATCC 10953.

272 Although previous studies have shown that ATCC 19606(T) cells acquire iron via the acinetobactin-m

273 The ATCC 14579 genome encodes an active enzyme Bce14579I (GC

274 corrected when complemented with either the ATCC 19606(T) parental allele or the Escherichia coli MG

275 in the omp33 gene (JPAB02), derived from the ATCC 17978 wild-type (wt).

276 Found in the ATCC 10987 strain, BceSI is a restriction endonuclease (

277 bactin intermediates in the virulence of the ATCC 19606(T) cells, although to a lesser extent when co

278 ion library resulted in the isolation of the ATCC 19606(T) derivative 1644, which was unable to grow

279 ations demonstrate that the virulence of the ATCC 19606(T) strain depends on the expression of a full

280 termined that the initial interaction of the ATCC 19606(T) type strain with A549 human alveolar epith

281 ctroscopy (ICP-AES) analyses showed that the ATCC 19606(T) NfuA ortholog has iron-binding properties

282 ical isolates reacted with antibodies to the ATCC 15305 CP.

283 coculture with P. gingivalis compared to the ATCC 35896 strain.

284 mes of the clinical isolates compared to the ATCC 35896 strain.

285 in the JPAB02 strain in competition with the ATCC 17978 wt, highlighting the effect of Omp33 on the m

286 ealyticum isolates were different from their ATCC serovar type strains and different within the same

287 g enzyme CteB, from Clostridium thermocellum ATCC 27405, with both SAM and an N-terminal fragment of

288 As a proof of concept, wild-type (ATCC 29212) and vancomycin-resistant Enterococcus cells

289 ram negative bacteria Salmonella typhimurium ATCC 13311.

290 faecalis ATCC 29212, Salmonella Typhimurium ATCC 14028, and Escherichia coli DH5alpha.

291 omonas putida KT2440, Salmonella Typhimurium ATCC 14028, Staphylococcus epidermidis ATCC 12228, Enter

292 vely with subspecies I (serovar Typhimurium) ATCC 14028 in vitro, to colonize Salmonella-sensitive BA

293 e two bacterial genomes, Anabaena variabilis ATCC 29413 and Haloquadratum walsbyi DSM 16790.

294 Anabaena variabilis ATCC 29413 fixes nitrogen in specialized cells called he

295 icity from that known in Anabaena variabilis ATCC 29413.

296 ted QC isolates were as follows: P. variotii ATCC MYA-3630, amphotericin B (15 to 24 mm), itraconazol

297 te each of five molds (Paecilomyces variotii ATCC MYA-3630, Aspergillus fumigatus ATCC MYA-3626, A. f

298 es lividans TK24 and Streptomyces venezuelae ATCC 10712, and detection of variant and incompletely pr

299 . polymorphum ATCC 10953, and ssp. vincentii ATCC 49256.

300 equenced from Streptomyces viridochromogenes ATCC 29814.