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

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

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

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

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

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

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

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

15 ferent Lactobacillus species (L. acidophilus ATCC 53544, L. casei ATCC 393, and L. reuteri ATCC 23272

16 hod, we engineered Lactobacillus acidophilus ATCC 4356 to display human CD4, the HIV-1 receptor, on t

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 niae ATCC 700603, and Pseudomonas aeruginosa ATCC 27853 were chosen as reference strains.

22 ady been developed in Pseudomonas aeruginosa ATCC 9027.

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

24 ized the putative SOR (FA796) from F. alocis ATCC 35896.

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

26 enic C. difficile strains (ATCC BAA 1870 and ATCC 43255), which yielded a hit compound, 2-methyl-8-ni

27 fection from 2 hvKp strains, NTUH K-2044 and ATCC 43816.

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

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

30 two strains of Escherichia coli (AW 1.7 and ATCC 25922).

31 evolutionary intermediate between Hall A and ATCC 3502.

32 erial vaginosis), were obtained from BEI and ATCC resources.

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

34 1,114 structural variants between the HN and ATCC strains.

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

36 0.015 mug/ml and 28 to 35 mm), and S. aureus ATCC 25923 (32 to 38 mm).

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

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

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

40 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

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

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

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

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

45 0.12 to 0.5 mug/ml for Staphylococcus aureus ATCC 29213, 0.25 to 2 mug/ml for Enterococcus faecalis A

46 ia coli ATCC 25922 and Staphylococcus aureus ATCC 29213, while DMPD chemiluminescence assay was used

47 t methicilin resistant Staphylococcus aureus ATCC 43300 and Candida albicans MTCC 227.

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

49 nt K. pneumoniae strains (NTUH-K2044, B5055, ATCC 43816, and RH201207), and explored their recognitio

50 vestigated strains Zygosaccharomyces bailii (ATCC 42476) and Aspergillus niger (ATCC 6275 (M68)).

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

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

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

54 minimum lethal dose required by A. baumannii ATCC 17978 DeltapstS was lower compared to the wild type

55 ious transcriptomic analysis of A. baumannii ATCC 17978 under microaerobiosis, we know the gene pstS

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

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

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

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

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

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

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

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

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

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

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

67 species (L. acidophilus ATCC 53544, L. casei ATCC 393, and L. reuteri ATCC 23272), with the aim of de

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

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

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

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

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

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

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

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

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

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

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

79 m thiocillin biosynthesis in Bacillus cereus ATCC 14579.

80 tibiotic-producing Streptomyces clavuligerus ATCC 27 064 is completed, which contains 7163 newly anno

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

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

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

84 Escherichia coli ATCC 25922, E. coli ATCC 35218, E. coli NCTC 13353, Klebsiella pneumoniae AT

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

86 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

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

88 imicrobial activity against Escherichia coli ATCC 25922 and Staphylococcus aureus ATCC 29213, while D

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

90 CC 29212, 1 to 4 mug/ml for Escherichia coli ATCC 25922, 0.12 to 0.5 mug/ml for Streptococcus pneumon

91 Escherichia coli ATCC 25922, E. coli ATCC 35218, E. coli NCTC 13353, Kleb

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

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

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

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

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

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

98 level of degradation of insulation concerned ATCC 25923.

99 ony-forming units of L lactis subsp cremoris ATCC 19257 or Lactobacillus rhamnosus GG ATCC 53103 (con

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

101 ding 20beta-HSDH in Butyricicoccus desmolans ATCC 43058 was reported, and a nonredundant protein sear

102 h the encapsulated HG184 or non-encapsulated ATCC 33277 strains of P. gingivalis were used as control

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

104 29213, 0.016 to 0.12 mug/ml for E. faecalis ATCC 29212, 0.008 to 0.03 mug/ml for S. pneumoniae ATCC

105 .004 to 0.015 mug/ml), Enterococcus faecalis ATCC 29212 (0.015 to 0.06 mug/ml), Pseudomonas aeruginos

106 (0.03 to 0.12 mug/ml), Enterococcus faecalis ATCC 29212 (0.03 to 0.12 mug/ml), and Streptococcus pneu

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

108 , 0.25 to 2 mug/ml for Enterococcus faecalis ATCC 29212, 1 to 4 mug/ml for Escherichia coli ATCC 2592

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

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

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

112 close relative of Streptomyces flavogriseus ATCC 33331.

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

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

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

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

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

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

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

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

121 ris ATCC 19257 or Lactobacillus rhamnosus GG ATCC 53103 (control bacteria) 3 times per week for 16 we

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

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

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

125 P. gingivalis (ATCC 33277) was grown in broth culture, and lipids were

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

127 anhydro-Neu5Ac is transported into R. gnavus ATCC 29149 before being converted back to Neu5Ac for fur

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

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

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

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

132 olygalacturonase from Streptomyces halstedii ATCC 10897.

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

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

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

136 3496(T), and 97.8% similarity to S. ictaluri ATCC BAA-1300(T).

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

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

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

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

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

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

143 or the type strain B. longum subsp. infantis ATCC 15697 (type strain) have been well characterized.

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

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

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

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

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

149 0.12 to 1 mug/ml for Haemophilus influenzae ATCC 49247.

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

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

152 v0189, from Streptomyces venezuelae ISP5230 (ATCC 10721) was characterized.

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

154 CdiIYkris complex from Yersinia kristensenii ATCC 33638.

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

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

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

158 human intestinal isolate Eubacterium limosum ATCC 8486, an acetogen that can grow by demethylation of

159 human intestinal isolate Eubacterium limosum ATCC 8486, an acetogen that excretes N-methyl proline du

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

161 d NRRL 3882 and Streptomyces lysosuperificus ATCC 31396.

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

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

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

165 model using the virulent Burkholderia mallei ATCC 23344 strain.

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

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

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

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

170 penA1) and bla (ampC1) in the B. multivorans ATCC 17616 background.

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

172 15, B. cenocepacia K56-2, and B. multivorans ATCC 17616 on 104 carbon sources.

173 eta-lactamases from Burkholderia multivorans ATCC 17616.

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

175 Four E. coli strains (NC11, ATCC 25922, CM-13457, and CM-10455) and one Klebsiella p

176 Ralstonia eutropha H16 (Cupriavidus necator ATCC 17699) uses l-ascorbate as sole carbon source via a

177 s bailii (ATCC 42476) and Aspergillus niger (ATCC 6275 (M68)).

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

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

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

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

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

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

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

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

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

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

188 -2-inducing strains in a DeltafadI mutant of ATCC 10953 resulted in hBD-2 induction to levels compara

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

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

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

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

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

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

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

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

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

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

199 t multi-drug resistant Klebsiella pneumoniae ATCC 700603 while isolates LB4 and LB41 showed pronounce

200 8, E. coli NCTC 13353, Klebsiella pneumoniae ATCC 700603, and Pseudomonas aeruginosa ATCC 27853 were

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

202 9212, 0.008 to 0.03 mug/ml for S. pneumoniae ATCC 49619, and 2 to 8 mug/ml for H. influenzae ATCC 492

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

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

205 29212 (broth only), Streptococcus pneumoniae ATCC 49619 (disk and broth), and Haemophilus influenzae

206 2 to 0.5 mug/ml for Streptococcus pneumoniae ATCC 49619, and 0.12 to 1 mug/ml for Haemophilus influen

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

208 zae ATCC 49247, and Streptococcus pneumoniae ATCC 49619.

209 quired for protection against K. pneumoniae (ATCC 43816) pulmonary infections.

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

211 am-positive bacterium Paenibacillus polymyxa ATCC 842 in Escherichia coli We found that PapP acts on

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

213 Nostoc punctiforme ATCC 29133 is a filamentous cyanobacterium that expresse

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

215 sis by the cyanobacterium Nostoc punctiforme ATCC 29133.

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

217 TCC 53544, L. casei ATCC 393, and L. reuteri ATCC 23272), with the aim of developing future strategie

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

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

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

221 lactic acid bacterium Lactobacillus reuteri ATCC PTA 6475.

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

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

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

225 odoccocus jostii RHA1, and Amycolatopsis sp. ATCC 39116.

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

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

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

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

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

231 diazotrophic cyanobacterium, Cyanothece sp. ATCC 51142.

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

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

234 Serratia sp. ATCC 39006 produces intracellular gas vesicles to enable

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

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

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

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

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

240 The Porphyromonas gingivalis strain ATCC 33277 (33277) and 381 genomes are nearly identical.

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

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

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

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

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

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

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

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

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

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

251 against the Neisseria gonorrhoeae QC strain ATCC 49226 was defined as 0.06 to 0.5 mug/ml and was app

252 .3 to 8.3%, relative to the reference strain ATCC 19977(T).

253 Serratia sp. strain ATCC 39006 (S39006) can float in aqueous environments du

254 chnology and showed strong binding to strain ATCC 19606.

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

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

257 e produced by Streptomyces venezuelae strain ATCC 15439.

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

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

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

261 against two pathogenic C. difficile strains (ATCC BAA 1870 and ATCC 43255), which yielded a hit compo

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

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

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

265 at lower UV-B doses, while Bacillus subtilis ATCC 6633 was more resistant to the treatment combinatio

266 subtilin producing strain Bacillus subtilis ATCC 6633.

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

268 robial activities against Bacillus subtilis (ATCC 6633) and two strains of Escherichia coli (AW 1.7 a

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

270 compared to the parent polymyxin-susceptible ATCC 19606.

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

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

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

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

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

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

277 26 induce significantly more hBD-2 mRNA than ATCC 10953.

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

279 el gyrase inhibitor zoliflodacin against the ATCC strains recommended by the Clinical and Laboratory

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

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

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

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

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

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

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

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

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

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

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

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

292 ram negative bacteria Salmonella typhimurium ATCC 13311.

293 marcescens in water, Salmonella Typhimurium ATCC 14028 was inoculated in water, 2% milk, almond milk

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

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

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

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

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

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

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

301 ss recognition by complement entirely, while ATCC 43816 and RH201207 were able to resist killing desp