ライフサイエンスコーパス: Lactococcus

1 , Bacillus, Streptococcus, Lactobacillus and Lactococcus.

2 to increased Lachnobacterium, but decreased Lactococcus.

3 14 alive probiotic strains (Lactobacillus + Lactococcus (6 x 10(10) CFU/g), Bifidobacterium (1 x 10(

4 ic activity relieves nitrogen limitation for Lactococcus and boosts de novo nucleotide biosynthesis.

5 s included enriched pyrotag populations from Lactococcus and Enterobacteriaceae relative to their fra

6 In this study, Northern analysis in both Lactococcus and Enterococcus backgrounds revealed that n

7 us, Listeria, Staphylococcus, Lactobacillus, Lactococcus and Leuconostoc do not have P450s, with the

8 Lactococcus and Streptococcus were predominant and corre

9 y bacteria, particularly those of the genera Lactococcus and Streptococcus, and a significant reducti

10 occus species and is incomplete in Listeria, Lactococcus, and Clostridium.

11 In addition, Lactobacillus, Escherichia, Lactococcus, and Muribacter were dominant in the lung mi

12 t; genera from Firmicutes (Faecalibacterium, Lactococcus, and Roseburia) correlated with faster colon

13 -Asx-L-Lys(3) in their cross-bridge, such as Lactococcus casei, Lactococcus lactis, and Enterococcus

14 d large contribution to the flavour profile, Lactococcus cremoris also played a role by limiting diac

15 fied in Lactococcus lactis subsp. lactis and Lactococcus cremoris subsp.

16 fied in Lactococcus lactis subsp. lactis and Lactococcus cremoris subsp. cremoris.

17 The largest genera (Lactococcus) decreased from 33.03% to 7.94%, while the A

18 Lactococcus garvieae is a Gram-positive coccus that has

19 -positive and Gram-negative bacteria, namely Lactococcus garvieae, Aeromonas salmonicida subsp. salmo

20 ed potential probiotic lactic acid bacteria, Lactococcus garvieae, isolated from camel milk.

21 s of the exopolysaccharide (EPS) produced by Lactococcus garvieae-C47 (exopolysaccharide-C47 product)

22 Lactococcus genus was a risk factor for asthma (adjusted

23 thermophilus has a crucial role in boosting Lactococcus growth and shaping flavour compound profile.

24 Attempts to clone the full-length cI gene in Lactococcus in the high-copy-number shuttle vector pTRKH

25 Staphylococcus, Corynebacterium, Pelomonas, Lactococcus, Lachnospiraceae (unclassified), and Faecali

26 f beta-cell autoantigens via the gut through Lactococcus lactis (L. lactis) has been demonstrated to

27 olved an efficient purification method using Lactococcus lactis (L. lactis), a generally recognized a

28 A homology model of the NADH oxidase from Lactococcus lactis (L.lac-Nox2) was also generated using

29 e in C57BL/6.NOD-Aec1Aec2 (SjS) females, the Lactococcus lactis (LL) 301 strain was developed to chro

30 bacterial delivery technology based on live Lactococcus lactis (LL) bacteria for controlled secretio

31 groups of NOD mice were orally treated with Lactococcus lactis (LL) expressing CFA/I.

32 actively in situ by the food-grade bacterium Lactococcus lactis (LL-IL-27), and tested its ability to

33 YaiB NADPH-dependent quinone reductase from Lactococcus lactis (YaiB), was developed to achieve rapi

34 ated sex factor that controls conjugation in Lactococcus lactis 712 has been cloned and sequenced, le

35 Salmonella typhimurium, the ATP-PRTase from Lactococcus lactis and a number of other bacterial speci

36 ent C (TTFC) was expressed constitutively in Lactococcus lactis and administered orally to C57 BL/6 m

37 e into intact cells and membrane vesicles of Lactococcus lactis and Bacillus subtilis is strongly inh

38 d, namely that described here and those from Lactococcus lactis and Caenorhabditis elegans.

39 erfamily multidrug-proton antiporter LmrP in Lactococcus lactis and developed a novel assay for the d

40 However, the AcpAs of Lactococcus lactis and Enterococcus faecalis were inacti

41 n heterologous host systems of esp-deficient Lactococcus lactis and Enterococcus faecium did not enha

42 the interaction between probiotic bacteria (Lactococcus lactis and Escherichia coli) and A498 human

43 ts (D) in the cytoplasm of Escherichia coli, Lactococcus lactis and Haloferax volcanii.

44 pon deletion of PIC2 Additionally, assays in Lactococcus lactis and in reconstituted liposomes direct

45 Microbiological (Lactococcus lactis and Lactobacillus acidophilus counts,

46 Two natural strains of Lactococcus lactis and one mutant were characterized in

47 This TS and the TSs from Lactococcus lactis and phage Phi3T-to which it is most s

48 Certain genes from Lactococcus lactis and Pseudomonas aeruginosa, including

49 viridae that includes at least phages r1t of Lactococcus lactis and SF370.3 of Streptococcus pyogenes

50 ns and Caulobacter crescentus), and Bacilli (Lactococcus lactis and Staphylococcus aureus).

51 In Lactococcus lactis and Staphylococcus carnosus, the ilvE

52 of E. faecalis and the heterologous bacteria Lactococcus lactis and Streptococcus gordonii was demons

53 m Saccharomyces cerevisiae were expressed in Lactococcus lactis and studied in inside-out membrane ve

54 occus pyogenes, Streptococcus pneumoniae and Lactococcus lactis are analyzed for abundances of short

55 ransposition events of the Ll.LtrB intron in Lactococcus lactis are into the plasmid donor.

56 We here report an expression system using Lactococcus lactis as a host for non-canonical amino aci

57 Ags, associated with the intake of probiotic Lactococcus lactis as tolerogenic adjuvant (combined the

58 The nisA promoter is positively regulated in Lactococcus lactis ATCC 11454 by autoinduction via a two

59 The recF gene of Lactococcus lactis ATCC 7962 is located 3 kb downstream

60 ulture of human intestinal cells with living Lactococcus lactis bacteria also was demonstrated in the

61 The collision events of single Lactococcus lactis bacteria at Pt disk ultramicroelectro

62 ned with oral gavage of genetically modified Lactococcus lactis bacteria secreting human proinsulin a

63 Low-dose anti-CD3 plus Lactococcus lactis bacteria secreting proinsulin and IL-

64 a biological membrane by expressing Gdt1p in Lactococcus lactis bacterial cells and by recording eith

65 A novel bacteriophage protection system for Lactococcus lactis based on a genetic trap, in which a s

66 Lactococcus lactis beta-phosphoglucomutase (beta-PGM) ca

67 Activated Lactococcus lactis beta-phosphoglucomutase (betaPGM) cat

68 e was addressed for the class 1A enzyme from Lactococcus lactis by determining kinetic isotope effect

69 superfamily multidrug transporter LmrP from Lactococcus lactis catalyses drug efflux in a membrane p

70 gordonii; another had 79% identity with the Lactococcus lactis clpE gene, encoding a member of the C

71 AATTTTCWGAAAATT motif, first identified for Lactococcus lactis CodY, with up to five mismatches play

72 eterologous expression of sof49 in M1 GAS or Lactococcus lactis conferred marked increases in HEp-2 c

73 Expression of the gene product in Lactococcus lactis conferred the ability to adhere to VK

74 on the surface of the non-adherent bacterium Lactococcus lactis confers adherence to scavenger recept

75 Here we construct synthetic Lactococcus lactis consortia and mathematical models to

76 The commercially important bacterium Lactococcus lactis contains two FNR-like proteins (FlpA

77 three T4SS-associated, putative hydrolases, Lactococcus lactis CsiA, Tn925 Orf14, and pIP501 TraG, p

78 the drug-sensitive, Gram-positive bacterium Lactococcus lactis Delta lmrA Delta lmrCD lacking major

79 al architecture of galactose mutarotase from Lactococcus lactis determined to 1.9-A resolution.

80 -dimensional structure of galactokinase from Lactococcus lactis determined to 2.1-A resolution.

81 the survival of the non-pathogenic bacterium Lactococcus lactis during a human whole blood killing as

82 nvestigated plant habitat-specific traits of Lactococcus lactis during growth in an Arabidopsis thali

83 The conjugative element pRS01 from Lactococcus lactis encodes the putative relaxase protein

84 B. bifidum PRL2010 appendages in nonpiliated Lactococcus lactis enhanced adherence to human enterocyt

85 mucosal-route administration of recombinant Lactococcus lactis expressing tetanus toxin fragment C (

86 Recent advances in the development of the Lactococcus lactis expression system have opened the way

87 A heterologous Lactococcus lactis expression system was used to express

88 4 NVDP and 38 NANP repeats) produced in the Lactococcus lactis expression system.

89 om phenotypic tests in yeast and produced in Lactococcus lactis for further biochemical characterizat

90 We examined the ability of Lactococcus lactis G121 to prevent allergic inflammatory

91 mutation to the recently solved structure of Lactococcus lactis GalK begins to provide a blueprint fo

92 l delivery in mice of biologically contained Lactococcus lactis genetically modified to secrete the w

93 nt vector (pHybrid I), a 20-kb fragment from Lactococcus lactis genomic DNA has been successfully int

94 cleoprotein (RNP) complex formed between the Lactococcus lactis group II intron and its self-encoded

95 tailed target site recognition rules for the Lactococcus lactis group II intron Ll.LtrB and to select

96 The Lactococcus lactis group II intron Ll.ltrB is similar to

97 n Escherichia coli expression system for the Lactococcus lactis group II intron Ll.LtrB to show that

98 In this work, we have trapped the native Lactococcus lactis group II intron RNP complex in its pr

99 For the pRS01 plasmid-encoded Lactococcus lactis group II intron, Ll.LtrB, splicing en

100 The genome of Lactococcus lactis has a multicistronic folate synthesis

101 ated beta-phosphoglucomutase (beta-PGM) from Lactococcus lactis has been determined to 2.3 A resoluti

102 f the PepF1 and PepF2 oligoendopeptidases of Lactococcus lactis has been identified in Bacillus subti

103 ffusion assays against the indicator strains Lactococcus lactis HP and Bacillus subtilis 6633.

104 Lactococcus lactis HR279 and JHK24 strains expressing hi

105 er of strains used in the FMP, we found that Lactococcus lactis I-1631 was sufficient to ameliorate c

106 e self-splicing group II Ll.LtrB intron from Lactococcus lactis into L. lactis 23S rRNA.

107 Previous studies of the Lactococcus lactis intron Ll.LtrB indicated that in its

108 te (ABC) transporter LmrA from the bacterium Lactococcus lactis is a homolog of the human multidrug r

109 beta-phosphoglucomutase (betaPGM) from Lactococcus lactis is a phosphoryl transfer enzyme requi

110 OpuA from Lactococcus lactis is a type I ABC-importer that uses tw

111 ss is species-specific as Acm2 purified from Lactococcus lactis is not glycosylated.

112 sus B 442, Lactobacillus rhamnosus 1937, and Lactococcus lactis JBB 500 were enriched with magnesium

113 h the nonpathogenic gram-positive bacterium, Lactococcus lactis K1, for the ability to survive in mou

114 The Lactococcus lactis L1.LtrB intron encodes a maturase, Lt

115 to manufacture model cheeses inoculated with Lactococcus lactis LD61.

116 lowing order: Enterococcus faecalis LDH2 </= Lactococcus lactis LDH2 < E. faecalis LDH1 < L. lactis L

117 The Lactococcus lactis Ll.LtrB group II intron encodes a rev

118 The Lactococcus lactis Ll.LtrB group II intron encodes a rev

119 Here, we analyzed the interaction of the Lactococcus lactis Ll.LtrB group II intron endonuclease

120 nalyzed DNA target-site requirements for the Lactococcus lactis Ll.LtrB group II intron in vitro and

121 The mobile Lactococcus lactis Ll.LtrB group II intron integrates in

122 The Lactococcus lactis Ll.LtrB group II intron retrohomes by

123 Here, we show that the Lactococcus lactis Ll.LtrB group II intron splices accur

124 The Lactococcus lactis Ll.LtrB group II intron uses a major

125 Here, we used databases of retargeted Lactococcus lactis Ll.LtrB group II introns and a compil

126 We previously showed that the group II Lactococcus lactis Ll.LtrB intron could retrotranspose i

127 everse transcriptase/maturase encoded by the Lactococcus lactis Ll.LtrB intron has a high affinity bi

128 site for the maturase (LtrA) encoded by the Lactococcus lactis Ll.LtrB intron is within a region of

129 Previous studies with the Lactococcus lactis Ll.LtrB intron suggested a model in w

130 Previous studies with the Lactococcus lactis Ll.LtrB intron suggested a model in w

131 e potentially involved in retrohoming of the Lactococcus lactis Ll.LtrB intron.

132 se region of the LtrA protein encoded by the Lactococcus lactis Ll.LtrB intron.

133 f homologous recombination, as found for the Lactococcus lactis Ll.LtrB intron.

134 igate the nature of substrate binding within Lactococcus lactis LmrP, a prototypical multidrug transp

135 acilitator superfamily transporter LmrP from Lactococcus lactis mediates protonmotive-force dependent

136 The chromosome of Lactococcus lactis MG 1363 contains a 60 kb conjugative

137 ing of a human gut metagenomic library using Lactococcus lactis MG1363 as heterologous host.

138 res of two Dps proteins (DpsA and DpsB) from Lactococcus lactis MG1363 reveal for the first time the

139 Two candidate probiotics, Lactococcus lactis NCC 2287 and Bifidobacterium lactis N

140 n with acid-producing and non-acid producing Lactococcus lactis NCIMB 9918 in UHT milk at 30 & 18 deg

141 AbiZ causes phage phi31-infected Lactococcus lactis NCK203 to lyse 15 min early, reducing

142 n combined with pTRK391 (P15A10::lacZ.st) in Lactococcus lactis NCK203, an antisense ORF2 construct w

143 ctionally expressed in the heterologous host Lactococcus lactis NZ9000, and the benefits of the newly

144 eport on three such systems in the bacterium Lactococcus lactis On the basis of sequence similarities

145 Escherichia coli, Pseudomonas aeruginosa and Lactococcus lactis on the surface of the 3D models revea

146 and functional studies on the inhibition of Lactococcus lactis PC (LlPC) by c-di-AMP.

147 purified one of these proteins, 67RuvC, from Lactococcus lactis phage bIL67 and demonstrated that it

148 es genes that are highly similar to those of Lactococcus lactis phage r1t and Streptococcus thermophi

149 also found in many bacteriophages, including Lactococcus lactis phage r1t.

150 Conjugative transfer of the Lactococcus lactis plasmid pRS01 requires splicing of a

151 nisin, simple synthetic circuits can direct Lactococcus lactis populations to form programmed spatia

152 Here we report that Lactococcus lactis possesses two different orthologues o

153 Certain strains of Lactococcus lactis produce the broad-spectrum bacterioci

154 Lactococcus lactis produces the lantibiotic nisin, which

155 otein and heterologous expression of SdrD in Lactococcus lactis promoted bacterial survival in human

156 ccharomyces cerevisiae) and in the bacterium Lactococcus lactis Protein production in these two micro

157 Heterologous expression of beta by Lactococcus lactis resulted in recruitment of FH to the

158 ging switch helix P1.1 in the representative Lactococcus lactis riboswitch.

159 catalytic module, and an endochitinase from Lactococcus lactis show that the nonprocessive enzymes h

160 colonized with recombinant PG overproducing Lactococcus lactis showed limited direct contribution of

161 vious studies in the Gram-positive bacterium Lactococcus lactis showed that heme exposure strongly in

162 Heterologous expression of Pic2 in Lactococcus lactis significantly enhanced CuL transport

163 rally-occurring plasmid pEW104 isolated from Lactococcus lactis ssp. cremoris W10.

164 The plasmid encoded LlaI R/M system from Lactococcus lactis ssp. lactis consists of a bidomain me

165 of pMRC01, a large conjugative plasmid from Lactococcus lactis ssp. lactis DPC3147, has been determi

166 small genome of the Gram-positive bacterium Lactococcus lactis ssp. lactis IL1403 contains two genes

167 is encoded on plasmid pJW566 and can protect Lactococcus lactis strains against bacteriophage infecti

168 Experimental evolution of several isogenic Lactococcus lactis strains demonstrated the existence of

169 Further, closely related Lactococcus lactis strains exhibited different interacti

170 Mice were then infected with Lactococcus lactis strains that differed only in SpyCEP

171 thermophiles, Lactobacillus bulgaricus, and Lactococcus lactis subsp Lactis.

172 s, including two lactic acid bacteria (i.e., Lactococcus lactis subsp.

173 Here, we report a new strain, Lactococcus lactis subsp.

174 e developed using the autochthonous cultures Lactococcus lactis subsp.

175 c amine production of two starter strains of Lactococcus lactis subsp. cremoris (strains from the Cul

176 Z32, Streptococcus thermophilus CNRZ302, and Lactococcus lactis subsp. cremoris AM2.

177 ecific integrase encoded by phage TP901-1 of Lactococcus lactis subsp. cremoris has potential as a to

178 ostoc mesenteroides subsp. jonggajibkimchii, Lactococcus lactis subsp. cremoris, Lactobacillus coryni

179 richia coli was also inhibited by 50% CFS of Lactococcus lactis subsp. lactis and 25% CFS of Leuconos

180 s were: QS - with culture Start, composed by Lactococcus lactis subsp. lactis and L. lactis subsp. cr

181 ne and 3-methyl-1-butanol were identified in Lactococcus lactis subsp. lactis and Lactococcus cremori

182 ne and 3-methyl-1-butanol were identified in Lactococcus lactis subsp. lactis and Lactococcus cremori

183 k passage structure of phage 340, a 936-type Lactococcus lactis subsp. lactis bacteriophage.

184 The native lactococcal plasmid, pKR223, from Lactococcus lactis subsp. lactis biovar diacetylactis KR

185 R2I restriction-modification (R-M) system of Lactococcus lactis subsp. lactis biovar diacetylactis KR

186 nfection immunity was conferred to the host, Lactococcus lactis subsp. lactis NCK203, indicating that

187 Recombinant HPP from Lactococcus lactis subsp. lactis that was expressed in E

188 4 residue lantibiotic produced by strains of Lactococcus lactis subsp. lactis, exerts antimicrobial a

189 aining bacteriocin (lantibiotic) produced by Lactococcus lactis subsp. lactis.

190 We assessed the effects of Lactococcus lactis subspecies (subsp) cremoris on weight

191 t constructed in the Gram-positive bacterium Lactococcus lactis subspecies lactis IL1403.

192 gative bacilli and gram-positive cocci, only Lactococcus lactis subspecies lactis produced extracellu

193 vivo performance of an engineered strain of Lactococcus lactis that altruistically degrades the wide

194 porter LmrA is a primary drug transporter in Lactococcus lactis that can functionally substitute for

195 ccine (LL-CRR) made from live, nonpathogenic Lactococcus lactis that expresses the conserved C-repeat

196 tator superfamily multidrug transporter from Lactococcus lactis that mediates the efflux of cationic

197 In Lactococcus lactis there is a protein, HisZ, in the hist

198 The use of Lactococcus lactis to deliver a chosen antigen to the mu

199 erial targets, and we transfer the system to Lactococcus lactis to establish its broad functionality

200 Using a heterologous expression system in Lactococcus lactis to overcome possible staphylococcal a

201 P and FNR in Escherichia coli were sought in Lactococcus lactis to provide a basis for redirecting ca

202 Lactococcus lactis transformed with plasmids expressing

203 Here, we present a Lactococcus lactis Trp auxotroph-based expression system

204 In contrast, Bacillus subtilis and Lactococcus lactis use manganese, and Saccharomyces cere

205 families infect the Gram-positive bacterium Lactococcus lactis using receptor-binding proteins ancho

206 Prediction of the function of HisZ in Lactococcus lactis was assisted by comparative genomics,

207 eptococcal virulence factors from M protein, Lactococcus lactis was engineered to express M1 protein

208 Lactococcus lactis was found to be the dominant bacteriu

209 n x-ray structure of the dimeric enzyme from Lactococcus lactis was recently solved and shown to be t

210 Expression of SfbA in the noninvasive strain Lactococcus lactis was sufficient to promote fibronectin

211 ptococcus mutans, Staphylococcus aureus, and Lactococcus lactis were examined for functional compleme

212 the chromosome of Lactobacillus reuteri and Lactococcus lactis without selection at frequencies rang

213 Lactococcus lactis YdbC is a representative of DUF2128.

214 Here, we characterize the Lactococcus lactis yybP-ykoY orphan riboswitch as a Mn(2

215 bind specifically to the Class 1A DHOD from Lactococcus lactis, 3,4-dihydroxybenzoate (3,4-diOHB) an

216 to a large family of Siphoviridae and infect Lactococcus lactis, a gram-positive bacterium used in co

217 ovalently anchored in the outer cell wall of Lactococcus lactis, a Gram-positive surrogate that other

218 .4% identity to the PepF oligopeptidase from Lactococcus lactis, a member of the M3 or thimet family

219 Lactococcus lactis, a non-pathogenic bacteria, has been

220 lis and also resulted in cCF10 production by Lactococcus lactis, a non-pheromone producer.

221 toward the bacteria Pseudomonas fluorescens, Lactococcus lactis, and 4 strains of the entomopathogen

222 Caenorhabditis elegans, Leishmania donovani, Lactococcus lactis, and Bacillus subtilis.

223 eir cross-bridge, such as Lactococcus casei, Lactococcus lactis, and Enterococcus faecium.

224 the Lactobacillus casei genome, expressed in Lactococcus lactis, and functionally characterized.

225 treptococcus mitis, Gemella parahaemolysans, Lactococcus lactis, and Fusobacterium nucleatum, were si

226 al tRNAs from the bacteria Escherichia coli, Lactococcus lactis, and Streptomyces griseus.

227 the new bacteria, Enterococcus faecalis and Lactococcus lactis, are gram positive.

228 athways of pyruvate metabolism of mutants of Lactococcus lactis, based on previously published experi

229 om YdbC, a prokaryotic PC4-like protein from Lactococcus lactis, but the underlying mechanism remains

230 In Lactococcus lactis, cell-wall polysaccharides (CWPSs) ac

231 . pyogenes, when expressed on surrogate host Lactococcus lactis, confers binding to immobilized saliv

232 enetic switch of TP901-1, a bacteriophage of Lactococcus lactis, controlled by the CI repressor and t

233 ble CK8 also bound to Staphylococcus aureus, Lactococcus lactis, Enterococcus faecalis, and Streptoco

234 AS in E. faecalis and the heterologous host Lactococcus lactis, experiments were designed to assess

235 on Microbiology Systems) were determined for Lactococcus lactis, L. garvieae, and unknown Lactococcus

236 er nectaris, Lactobacillus sanfranciscensis, Lactococcus lactis, Lactococcus piscium, Lactococcus pla

237 The mobile group II intron of Lactococcus lactis, Ll.LtrB, provides the opportunity to

238 Using Escherichia coli, Lactococcus lactis, Mycobacterium smegmatis, Lactobacill

239 Genetically modified Lactococcus lactis, non-pathogenic bacteria expressing t

240 teri, L. acidophilus, a Bifidobacterium sp., Lactococcus lactis, or a Bacillus sp. developed IBD duri

241 ted for their antimicrobial activity against Lactococcus lactis, Staphylococcus aureus, Listeria mono

242 on, Pearson correlation analysis showed that Lactococcus lactis, Staphylococcus, Trichococcus, and Mo

243 s, Listeria monocytogenes, Listeria innocua, Lactococcus lactis, Streptococcus pyogenes, Streptococcu

244 e is introduced into the commensal bacterium Lactococcus lactis, the truncated CBD is also produced,

245 oral vaccination with a probiotic organism, Lactococcus lactis, to elicit HIV-specific immune respon

246 e for the maintenance of this equilibrium in Lactococcus lactis, we isolated mutants that are resista

247 dihydroorotate dehydrogenase A (DHODA) from Lactococcus lactis, were characterized by employing sing

248 alculate CCRs for ~100-200 enzymes each from Lactococcus lactis, yeast, and Arabidopsis CCRs in these

249 gen captured on the surface of S. aureus- or Lactococcus lactis-expressing FnBPB could be activated t

250 of the biotin-specific S component BioY from Lactococcus lactis.

251 fied Shr or intranasally with Shr-expressing Lactococcus lactis.

252 the pilB gene in the nonpathogenic bacterium Lactococcus lactis.

253 related bacteria, Enterococcus faecalis and Lactococcus lactis.

254 f the otherwise unrelated plasmid pRS01 from Lactococcus lactis.

255 of the regulation of glucose utilization in Lactococcus lactis.

256 for a high-efficiency conjugation process in Lactococcus lactis.

257 es to cellular poles in Escherichia coli and Lactococcus lactis.

258 pressed on the surface of the surrogate host Lactococcus lactis.

259 peptidases from Lactobacillus helveticus and Lactococcus lactis.

260 te with the prototypical family 1A DHOD from Lactococcus lactis.

261 ve studied the bacterial L1.LtrB intron from Lactococcus lactis.

262 beta-hemolytic phenotype to the nonhemolytic Lactococcus lactis.

263 acillus subtilis, Listeria monocytogenes and Lactococcus lactis.

264 isin is an antimicrobial peptide produced by Lactococcus lactis.

265 showed sequence similarities to LCNDR2 from Lactococcus lactis.

266 of CdnG and Cap5, from Asticcacaulis sp. and Lactococcus lactis.

267 c that is similar to the nisin-A produced by Lactococcus lactis.

268 ge and coexist in a culture of the bacterium Lactococcus lactis.

269 with the putative active-site base Cys130 of Lactococcus lactisDHODase.

270 Key microbial species, including Lactococcus, Lactobacillus, Acetobacter, and Lacticaseib

271 Our data revealed that Lactococcus, Lactobacillus, and Coprococcus protect the

272 However, Lactococcus latics subsp. lactis strain X and Lactobacil

273 fied 6 genera (Acinetobacter, Lactobacillus, Lactococcus, Leuconostoc, Saccharomyces and Zymomonas) a

274 Microbial counts (Lactobacillus, Lactococcus, Leuconostoc, yeast), antagonistic activity

275 scillospira (log2 fold change -2.80, P=.03), Lactococcus (log2 fold change -3.19, P=.05), and Dorea (

276 mice had increased Serratia (P < 0.001) and Lactococcus (P < 0.05) whereas MF mice had increased Lac

277 riate modeling using the most discriminating Lactococcus phages could better predict alcohol use in t

278 The relative abundance of several Lactococcus phages was more similar between AUD patients

279 cillus sanfranciscensis, Lactococcus lactis, Lactococcus piscium, Lactococcus plantarum, Leuconostoc

280 is, Lactococcus lactis, Lactococcus piscium, Lactococcus plantarum, Leuconostoc citreum, Leuconostoc

281 atibacter (R2 = 22.4%; 95% CI, 22.1%-22.8%), Lactococcus (R2 = 21.6%; 95% CI, 20.9%-22.3%), and Haemo

282 , including Enterococcus, Streptococcus, and Lactococcus sp.

283 asma sp., Spirosoma sp., Roseomonas sp., and Lactococcus sp. were present only in throughfall samples

284 lindamycin, indicating that knowledge of the Lactococcus species causing an infection might influence

285 iophage infection mechanism that can protect Lactococcus species from infection by a variety of bacte

286 t the most reproducible signals of a HFD are Lactococcus species, which we experimentally demonstrate

287 Lactococcus lactis, L. garvieae, and unknown Lactococcus species.

288 the PepV gene family from Lactobacillus and Lactococcus spp.

289 ive Clostridium spp., Enterococcus spp., and Lactococcus spp.

290 the PepX gene family from Lactobacillus and Lactococcus spp. and putative x-prolyl dipeptidyl-peptid

291 syl substituents (those of Listeria spp. and Lactococcus spp.) were poor ligands.

292 ely to confer phage resistance in commercial Lactococcus starter cultures.

293 ntations with systematic exclusion of single Lactococcus strains, combined with genomics, genome-scal

294 re containing Streptococcus thermophilus and Lactococcus strains.

295 conostoc, Staphylococcus, Streptococcus, and Lactococcus were predominant in colostrum samples, where