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1 rification on a Ni-NTA column to interact in Streptomyces lividans .
2 ts heterologous expression in the model host Streptomyces lividans.
3 , assembled, and expressed heterologously in Streptomyces lividans.
4 be produced in Streptomyces albus but not in Streptomyces lividans.
5  using ribosomes and ribosomal subunits from Streptomyces lividans.
6 stal structure of a K(+) channel (KcsA) from Streptomyces lividans.
7 Thermobifida fusca into Escherichia coli and Streptomyces lividans.
8  cloned and expressed in Escherichia coli or Streptomyces lividans.
9 of a bacterial K(+) channel: i.e., KcsA from Streptomyces lividans.
10 stal structure of the KcsA K(+) channel from Streptomyces lividans.
11 ated, and the mutant genes were expressed in Streptomyces lividans.
12 rified from overexpression of their genes in Streptomyces lividans.
13 e (TM) segments was recently identified from Streptomyces lividans.
14 (MC) and related mitomycins when cloned into Streptomyces lividans.
15 fer of both chromosomal and plasmid genes in Streptomyces lividans.
16 ptions of rnc in both S. coelicolor 1501 and Streptomyces lividans 1326 caused an Abs(-) phenotype.
17 nd showed a high degree of similarity to the Streptomyces lividans 1326 mercury resistance operon.
18  cluster to the pentalenolactone nonproducer Streptomyces lividans 1326 resulted in production of pen
19 abies ATCC 41973 that allows the nonpathogen Streptomyces lividans 66 TK24 to necrotize and colonize
20  It had been shown by Southern blotting that Streptomyces lividans, a close relative of S. coelicolor
21 128 gene cluster was cloned and expressed in Streptomyces lividans, a genetically well developed hete
22 se five genes in Streptomyces avermitilis or Streptomyces lividans allows for production of significa
23 he vph AUG translational start codon in both Streptomyces lividans and E. coli; cells expressing the
24                                         Both Streptomyces lividans and Streptomyces avermitilis encod
25                                         Both Streptomyces lividans and Streptomyces avermitilis have
26 n the two closely related bacterial species, Streptomyces lividans and Streptomyces coelicolor, it no
27 treptomyces lavendulae) were introduced into Streptomyces lividans and transformants were selected fo
28 ent Actinobacteria (Mycobacterium smegmatis, Streptomyces lividans, and Rhodococcus jostii) each exhi
29 binant alpha-L-arabinofuranosidase gene from Streptomyces lividans are readily identified by visual i
30 er sphaeroides, and the potassium channel of Streptomyces lividans) are studied to address the role o
31 o use KcsA (a K(+) channel from the bacteria Streptomyces lividans) as a surrogate because it lacks a
32            Expression of AMO was achieved in Streptomyces lividans by cloning the AMO genes into the
33 o it is not surprising that bacteria such as Streptomyces lividans can activate many of the available
34         The bacterial K(+) channel KcsA from Streptomyces lividans can be used to help elucidate ques
35 ion similar to that seen in the structure of Streptomyces lividans CelB2 complexed with an inhibitor.
36  throughout development of pIJ101-containing Streptomyces lividans cells, with the concentration of K
37 lasmid pIJ101 of the spore-forming bacterium Streptomyces lividans contains a regulatory gene, korB,
38 ressor protein (CsoR) has been identified in Streptomyces lividans (CsoR(Sl)) and found to regulate c
39 e use a structurally characterized CsoR from Streptomyces lividans (CsoR(Sl)) together with three spe
40                              The ppk gene of Streptomyces lividans encodes an enzyme catalyzing, in v
41           Heterologous expression of fkbM in Streptomyces lividans established that fkbM encodes an O
42 6 of the full DEBS gene set and expressed in Streptomyces lividans for in vivo analysis.
43              Since introduction of drrC into Streptomyces lividans imparted a DNR resistance phenotyp
44  structure of the tetrameric K+ channel from Streptomyces lividans in a lipid bilayer environment was
45                   The potassium channel from Streptomyces lividans is an integral membrane protein wi
46  Here we report the crystal structure of the Streptomyces lividans K(+) channel KcsA in its open-inac
47   The selectivity filter is identical to the Streptomyces lividans K(+) channel within error of measu
48  built by homology with the structure of the Streptomyces lividans K+ channel KcsA, suggested the exi
49 sed and manipulated in the heterologous host Streptomyces lividans K4-114.
50 C-1027 and calicheamicin cognate PKSE-TEs in Streptomyces lividans K4-114; and (iii) selected native
51                                              Streptomyces lividans KcsA is a 160-aa polypeptide that
52                                          The Streptomyces lividans KcsA potassium channel, a homotetr
53 along the narrow pore of the K+ channel from Streptomyces lividans (KcsA), suggesting that K+ ions mi
54 he selectivity filter of the K+ channel from Streptomyces lividans (KcsA).
55 ologous expression of the megalomicin PKS in Streptomyces lividans led to production of 6-deoxyerythr
56 e, we report that rescue of such plasmids in Streptomyces lividans occurs by three distinct types of
57                      Endoglucanase CelB from Streptomyces lividans performs hydrolysis of the beta-1,
58 vealed extensive sequence similarity between Streptomyces lividans plasmid pIJ101 and Streptomyces pl
59                              The tra gene of Streptomyces lividans plasmid pIJ101 encodes a 621-amino
60  by refolding distorted conformations of the Streptomyces lividans potassium channel (KcsA), correspo
61 structural basis of activation gating in the Streptomyces lividans potassium channel (KcsA).
62 ipA, a MerR family transcription factor from Streptomyces lividans, promotes antibiotic resistance by
63 e enterocin biosynthesis genes encABCDLMN in Streptomyces lividans resulted in the formation of the r
64                 Expression of these genes in Streptomyces lividans resulted in the production of ala(
65 ed high level simocyclinone D8 resistance on Streptomyces lividans, showing that simX encodes a simoc
66 uxiliary activity family 10 (AA10) LPMO from Streptomyces lividans (SliLPMO10E).
67 omyces coelicolor, Streptomyces avermitilis, Streptomyces lividans, Streptomyces tsukubaensis, Strept
68  to the thiostrepton-induced protein TipA of Streptomyces lividans strongly suggest that Mta is an au
69 ion that induced prodiginine production from Streptomyces lividans, suggesting differential regulatio
70 AT8 and the engineered gene was expressed in Streptomyces lividans, the strain produced 6-deoxyerythr
71 uring promoter-probe analysis carried out in Streptomyces lividans, the TylP protein powerfully inhib
72 nsis UC 5144, its heterologous expression in Streptomyces lividans TK24 and Streptomyces venezuelae A
73                                  Extracts of Streptomyces lividans TK24 containing recombinant DauE c
74 P were sufficient and necessary to confer on Streptomyces lividans TK24 the ability to convert rhodom
75       After transfer of the four clusters to Streptomyces lividans TK24, expression of one cluster fr
76  activity screening a genomic DNA library in Streptomyces lividans TK24.
77  transferred from Streptomyces coelicolor or Streptomyces lividans to Mycobacterium smegmatis mc2155
78 transcriptional activator in the response of Streptomyces lividans to the peptide antibiotic thiostre
79 e establishment of pSLA2 in circular form in Streptomyces lividans transformants.
80 binant DoxA was purified to homogeneity from Streptomyces lividans transformed with a plasmid contain
81                                  A strain of Streptomyces lividans transformed with all three plasmid
82 pression of this gene, named herein doxA, in Streptomyces lividans TY24 resulted in in vivo bioconver
83           Using heterologous biosynthesis in Streptomyces lividans, we also determined that biosynthe
84         Previously, in engineered strains of Streptomyces lividans, we showed that TylP, a deduced ga
85 nd PepN2, two neighboring PepN homologs from Streptomyces lividans were purified in E. coli but displ
86      Resin-attached, mutant K+ channels from Streptomyces lividans were used to screen venom from Lei
87 itution mutants of KcsA, a K(+) channel from Streptomyces lividans, were expressed in Escherichia col
88 ram-positive bacteria, Bacillus subtilis and Streptomyces lividans, while capable of specifically int
89 f Actinosynnema pretiosum was coexpressed in Streptomyces lividans with the genes encoding the 6-deox
90           Here we identify SlPatA, a GNAT in Streptomyces lividans with unique domain organization, a
91 griseochromogenes or a heterologous producer Streptomyces lividans WJ2.
92 sing tpgR1 to probe a genomic DNA library of Streptomyces lividans ZX7, whose linear chromosome can u