ライフサイエンスコーパス: Lactococcus

1 to increased Lachnobacterium, but decreased Lactococcus.

2 , Bacillus, Streptococcus, Lactobacillus and Lactococcus.

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

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

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

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

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

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

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

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

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

12 Lactococcus garvieae is a Gram-positive coccus that has

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

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

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

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

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

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

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

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

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

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

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

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

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

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

27 Microbiological (Lactococcus lactis and Lactobacillus acidophilus counts,

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

29 Certain genes from Lactococcus lactis and Pseudomonas aeruginosa, including

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

31 In Lactococcus lactis and Staphylococcus carnosus, the ilvE

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

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

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

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

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

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

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

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

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

41 Activated Lactococcus lactis beta-phosphoglucomutase (betaPGM) cat

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

60 A heterologous Lactococcus lactis expression system was used to express

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

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

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

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

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

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

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

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

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

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

71 The genome of Lactococcus lactis has a multicistronic folate synthesis

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

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

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

75 Lactococcus lactis HR279 and JHK24 strains expressing hi

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

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

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

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

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

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

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

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

84 to manufacture model cheeses inoculated with Lactococcus lactis LD61.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

118 Lactococcus lactis produces the lantibiotic nisin, which

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

143 4 residue lantibiotic produced by strains of Lactococcus lactis subsp. lactis, exerts antimicrobial a

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

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

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

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

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

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

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

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

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

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

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

155 Lactococcus lactis transformed with plasmids expressing

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

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

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

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

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

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

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

163 Lactococcus lactis YdbC is a representative of DUF2128.

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

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

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

167 .4% identity to the PepF oligopeptidase from Lactococcus lactis, a member of the M3 or thimet family

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

189 related bacteria, Enterococcus faecalis and Lactococcus lactis.

190 f the otherwise unrelated plasmid pRS01 from Lactococcus lactis.

191 of the regulation of glucose utilization in Lactococcus lactis.

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

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

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

195 peptidases from Lactobacillus helveticus and Lactococcus lactis.

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

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

198 beta-hemolytic phenotype to the nonhemolytic Lactococcus lactis.

199 acillus subtilis, Listeria monocytogenes and Lactococcus lactis.

200 isin is an antimicrobial peptide produced by Lactococcus lactis.

201 showed sequence similarities to LCNDR2 from Lactococcus lactis.

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

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

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

205 the pilB gene in the nonpathogenic bacterium Lactococcus lactis.

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

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

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

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

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

211 , including Enterococcus, Streptococcus, and Lactococcus sp.

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

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

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

215 the PepV gene family from Lactobacillus and Lactococcus spp.

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

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

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

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

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