ライフサイエンスコーパス: Lactococcus lactis

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

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

3 peptidases from Lactobacillus helveticus and Lactococcus lactis.

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

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

6 beta-hemolytic phenotype to the nonhemolytic Lactococcus lactis.

7 acillus subtilis, Listeria monocytogenes and Lactococcus lactis.

8 isin is an antimicrobial peptide produced by Lactococcus lactis.

9 showed sequence similarities to LCNDR2 from Lactococcus lactis.

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

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

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

13 the pilB gene in the nonpathogenic bacterium Lactococcus lactis.

14 related bacteria, Enterococcus faecalis and Lactococcus lactis.

15 f the otherwise unrelated plasmid pRS01 from Lactococcus lactis.

16 of the regulation of glucose utilization in Lactococcus lactis.

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

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

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

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

21 .4% identity to the PepF oligopeptidase from Lactococcus lactis, a member of the M3 or thimet family

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

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

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

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

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

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

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

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

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

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

32 Microbiological (Lactococcus lactis and Lactobacillus acidophilus counts,

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

34 Certain genes from Lactococcus lactis and Pseudomonas aeruginosa, including

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

36 In Lactococcus lactis and Staphylococcus carnosus, the ilvE

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

52 Activated Lactococcus lactis beta-phosphoglucomutase (betaPGM) cat

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

75 A heterologous Lactococcus lactis expression system was used to express

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

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

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

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

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

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

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

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

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

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

86 The genome of Lactococcus lactis has a multicistronic folate synthesis

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

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

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

90 Lactococcus lactis HR279 and JHK24 strains expressing hi

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

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

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

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

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

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

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

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

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

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

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

102 to manufacture model cheeses inoculated with Lactococcus lactis LD61.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

141 Lactococcus lactis produces the lantibiotic nisin, which

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

167 4 residue lantibiotic produced by strains of Lactococcus lactis subsp. lactis, exerts antimicrobial a

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

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

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

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

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

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

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

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

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

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

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

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

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

181 Lactococcus lactis transformed with plasmids expressing

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

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

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

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

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

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

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

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

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

191 Lactococcus lactis YdbC is a representative of DUF2128.

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