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1 the lac UV5 promoter or the PR promoter from bacteriophage lambda.
2  of multiple modifications on the surface of bacteriophage lambda.
3 urements of single DNA molecule packaging in bacteriophage lambda.
4 ld higher than ejection forces measured with bacteriophage lambda.
5 ation signal, to an RNA binding peptide from bacteriophage lambda.
6  perspective on the lysis/lysogeny switch of bacteriophage lambda.
7 lls to foster lytic growth by red gam mutant bacteriophage lambda.
8 ble for maltose uptake and for attachment of bacteriophage lambda.
9 ase required for homologous recombination by bacteriophage lambda.
10 -mediated homologous recombination system of bacteriophage lambda.
11 r a complete narrative for the life cycle of bacteriophage lambda.
12  transcription through the tR2 terminator of bacteriophage lambda.
13 , a multifragment chloroplast DNA probe, and bacteriophage lambda.
14 ed for the naturally leaderless cI mRNA from bacteriophage lambda.
15 35 consensus regions of the P(R) promoter of bacteriophage lambda.
16 on of the N and Q antiterminator proteins of bacteriophage lambda.
17 ages M13 or phiX174 nor of Uracil-containing bacteriophage lambda.
18 lease activity of the model exonuclease from bacteriophage lambda.
19  and their homologues in the closely related bacteriophage lambda.
20 assembly inhibitory factors including Kil of bacteriophage lambda.
21 sically disordered protein, the N protein of bacteriophage lambda.
22 inor capsid protein UL25 in HSV-1 and gpD in bacteriophage lambda.
23 hanistic studies on the terminase motor from bacteriophage lambda.
24 UUAU-3' from the tR2 intrinsic terminator of bacteriophage lambda.
25 ern the dynamics of in vitro DNA ejection in bacteriophage lambda.
26  single-molecule studies of DNA packaging in bacteriophage lambda.
27 vailing notions in this postgenomic era, the bacteriophage lambda, a paragon of simplicity, may still
28                                We propagated bacteriophage lambda, a virus with rapid generations and
29                             The N protein of bacteriophage lambda activates expression of the delayed
30                                 Protein N of bacteriophage lambda activates the lytic phase of phage
31              The tetrameric cII protein from bacteriophage lambda activates transcription from the ph
32                             The N protein of bacteriophage lambda activates transcription of genes th
33                          The beta protein of bacteriophage lambda acts in homologous genetic recombin
34    We consider a single network derived from bacteriophage lambda and construct a two-parameter deter
35                           The development of bacteriophage lambda and double-stranded DNA viruses in
36                        We have used a set of bacteriophage lambda and Escherichia coli replication pr
37  infection of Escherichia coli bacteria with bacteriophage lambda and following the establishment of
38                                         Both bacteriophage lambda and herpes simplex virus (HSV) disp
39 situations: on the chromosome of E. coli, in bacteriophage lambda and in high-copy-number pUC-based p
40                             The repressor of bacteriophage lambda and its homolog, LexA, preferential
41 hia coli strains expressing the red genes of bacteriophage lambda and lacking recBCD function either
42 y of peptides and proteins on the surface of bacteriophage lambda and to facilitate the use of modifi
43                                 I began with bacteriophage lambda and tried to establish the colinear
44       We used the recombination systems from bacteriophages lambda and P1 to engineer each strain in
45                                The temperate bacteriophages lambda and P22 share similarities in thei
46 tained from pure samples of adenovirus, from bacteriophages lambda and T4 GT7, and from a mixture of
47  regulatory pause of the late gene operon of bacteriophage lambda, and that this process is enhanced
48 lity and induction of the lysogenic state of bacteriophage lambda are balanced by a complex regulator
49 s of the decision structure in the temperate bacteriophage lambda are consistent with our conclusions
50 e results to the process of DNA packaging in bacteriophage lambda are discussed.
51 iochemical studies on genome packaging using bacteriophage lambda as a model system.
52 g to elucidate the target-finding process in bacteriophage lambda as it infects an Escherichia coli c
53 , together with a complex functional role in bacteriophage lambda assembly, suggest that gpW has been
54      We follow the postinfection decision in bacteriophage lambda at single-virus resolution, and sho
55 ia include (a) Red recombination mediated by bacteriophage lambda, (b) integration of group II mobile
56                                              Bacteriophage lambda begins its infection cycle by eject
57 in of prophage HK022 excludes superinfecting bacteriophage lambda by blocking transcription elongatio
58 of hydrodynamically sheared genomic DNA from bacteriophage lambda can be amplified linearly.
59 s located downstream of the p(L) promoter of bacteriophage lambda can induce cell-cycle synchrony in
60      Herpes simplex type 1 virus (HSV-1) and bacteriophage lambda capsids undergo considerable struct
61 ical stability of gpD-free and gpD-decorated bacteriophage lambda capsids.
62             The integrase protein (Int) from bacteriophage lambda catalyzes the insertion and excisio
63     Crosses between a non-replicating linear bacteriophage lambda chromosome and a replicating plasmi
64                          The cos site of the bacteriophage lambda chromosome contains the sites requi
65 -specific recombination pathway by which the bacteriophage lambda chromosome is excised from its Esch
66 eaction used to site-specifically excise the bacteriophage lambda chromosome out of its E. coli host
67                                              Bacteriophage lambda chromosomes are processively packag
68 exclusively on the isomerization step is the bacteriophage lambda cI protein (lambdacI), which has be
69 o different DNA-binding domains, that of the bacteriophage lambda cI protein and that of the Escheric
70 re, we use long-range gene regulation by the bacteriophage lambda CI protein as a powerful system to
71                              We replaced the bacteriophage lambda cI repressor C-terminal dimerizatio
72 rization via their abilities to dimerize the bacteriophage lambda cI repressor DNA-binding domain.
73 1 self-association was demonstrated by using bacteriophage lambda cI repressor fusion and pull-down a
74                            An example is the bacteriophage lambda cI repressor, a dimeric protein tha
75  as an example the directed evolution of the bacteriophage lambda cI TF against two synthetic bidirec
76 witches for orthogonal logic gates, based on bacteriophage lambda cI variants and multi-input promote
77                                          The bacteriophage lambda CII protein stimulates the activity
78 ere used as a reagent to isolate recombinant bacteriophage lambda clones expressing antigens of the o
79               The long flexible tail tube of bacteriophage lambda connects its capsid to the tail tip
80 enerated all eight possible code variants of bacteriophage lambda Cro and used electrophoretic mobili
81                  The overall affinity of the bacteriophage lambda Cro repressor for its operator DNA
82 l protein homodimers (bacteriophage N15 Cro, bacteriophage lambda Cro, and bacteriophage P22 Arc) wit
83 tions affects the lysis-lysogeny decision of bacteriophage lambda despite variable infection times be
84                      The "genetic switch" of bacteriophage lambda determines whether a prophage stays
85              The p(R) and p(RM) promoters of bacteriophage lambda direct transcription in divergent d
86 plify 199- and 500-base pair (bp) regions of bacteriophage lambda DNA and 346- and 410-bp regions of
87 n-chip PCR/CE analysis of a 500-bp region of bacteriophage lambda DNA was also demonstrated.
88 t with these steady-state kinetic data, when bacteriophage lambda DNA was used as a substrate, maxima
89  required for site-specific recombination of bacteriophage lambda DNA.
90  cI repressors at the right operator (OR) of bacteriophage lambda DNA.
91 li, DnaK is essential for the replication of bacteriophage lambda DNA; this in vivo activity provides
92                 Efficient expression of most bacteriophage lambda early genes depends upon the format
93 ichia coli by homologous recombination using bacteriophage lambda-encoded enzymes.
94       Such recombination is possible because bacteriophage lambda-encoded functions, called Red, effi
95                                          The bacteriophage lambda-encoded site-specific recombinase i
96                                              Bacteriophage lambda encodes a 28 kDa protein called bet
97                                              Bacteriophage lambda encodes a DNA recombination system
98           To counteract the latter activity, bacteriophage lambda encodes a small protein inhibitor c
99                          To avoid this fate, bacteriophage lambda encodes the gene Gam whose product
100                     We examined how a virus, bacteriophage lambda, evolved to infect its host, Escher
101                                          The bacteriophage lambda excisionase (Xis) protein is requir
102  digestion of lambda-phage DNA by individual bacteriophage lambda exonuclease molecules.
103 nsiently formed in situ at the metal core of Bacteriophage-lambda Exonuclease (Exo-lambda), during ca
104                                            A bacteriophage lambda fragment and the Igf2r DMR2 showed
105                              The orf gene of bacteriophage lambda, fused to a promoter, was placed in
106                                              Bacteriophage lambda gene Q protein and the related prot
107                                          The bacteriophage lambda genetic switch is still yielding su
108 ing, for example, derives in large part from bacteriophage lambda genetics.
109 n origin of replication and a segment of the bacteriophage lambda genome comprising the red genes (ex
110 ident below 6000 basepairs for unzipping the bacteriophage lambda-genome.
111                  The CW02 capsid consists of bacteriophage lambda gpD-like densities that likely cont
112                                              Bacteriophage lambda had two distinct peaks in its size
113                         The Cro protein from bacteriophage lambda has a dimeric alpha+beta fold that
114                                              Bacteriophage lambda has for many years been a model sys
115                                              Bacteriophage lambda has four adjacent genes -S, R, Rz a
116                                 The study of bacteriophage lambda has provided key insights into fund
117                                              Bacteriophage lambda has served as an ideal model system
118  their functional similarities to the lambda bacteriophage (lambda) holin.
119 influence the lysis-lysogeny decision of the bacteriophage lambda(imm434).
120                      Genetic elements in the bacteriophage lambda immunity region contribute to stabl
121        The structure of the Cro protein from bacteriophage lambda in complex with a 19 base-pair DNA
122 s the quiescent (lysogenic) transcriptome of bacteriophage lambda in infected Escherichia coli.
123 ia coli chromosomes bearing the red genes of bacteriophage lambda in place of recBCD was tested in st
124 s were screened for the ability to propagate bacteriophage lambda in the background of a dnaK deficie
125 sically disordered protein, the N protein of bacteriophage lambda, in the presence of high concentrat
126 is different from what occurs in the related bacteriophage lambda, in which binding of lambda repress
127 ted in the random lysis/lysogeny decision of bacteriophage-lambda, in the loss of synchrony of circad
128                                              Bacteriophage lambda infection of Escherichia coli can r
129 aking is derived from simple models, such as bacteriophage lambda infection, in which lambda chooses
130                                              Bacteriophage lambda integrase (Int) catalyzes at least
131                                              Bacteriophage lambda integrase (Int) catalyzes site-spec
132                                              Bacteriophage lambda integrase (Int) catalyzes the integ
133                                              Bacteriophage lambda integrase (Int) is a versatile site
134     Site-specific recombination catalyzed by bacteriophage lambda integrase (Int) is essential for es
135 rformed by tyrosine recombinases such as the bacteriophage lambda Integrase (Int) protein.
136 ccumulation of natural Holliday junctions of bacteriophage lambda Integrase (Int)-mediated reactions.
137 ecombinase family of enzymes, which includes bacteriophage lambda Integrase (Int).
138                                              Bacteriophage lambda integrase (lambda-Int) is the proto
139                                              Bacteriophage lambda integrase (lambda-Int), a phage-enc
140                                          The bacteriophage lambda integrase catalyzes four site-speci
141 for site-specific recombination catalysed by bacteriophage Lambda Integrase protein (Int).
142                                          The bacteriophage lambda integrase protein (lambda Int) belo
143 cific recombination reaction mediated by the bacteriophage lambda integrase protein.
144 lexes similar to intasomes, which consist of bacteriophage lambda integrase, Escherichia coli integra
145 res similarities with the well-characterized bacteriophage lambda integration, Cre-lox is in many way
146 tor include partition of the cI repressor of bacteriophage lambda into two functional domains separat
147                          The c1 repressor of bacteriophage lambda is a classic example of a protein t
148                                          The bacteriophage lambda is a convenient source of high qual
149                                              Bacteriophage lambda is a double-stranded DNA virus that
150                                              Bacteriophage lambda is a double-stranded DNA virus that
151       The site-specific recombinase (Int) of bacteriophage lambda is a heterobivalent DNA-binding pro
152       The site-specific recombinase (Int) of bacteriophage lambda is a heterobivalent DNA-binding pro
153                           The N protein from bacteriophage lambda is a key regulator of transcription
154                                              Bacteriophage lambda is a paradigm for understanding the
155                             The Q protein of bacteriophage lambda is a transcription antiterminator t
156                       The cro repressor from bacteriophage lambda is an important and classical trans
157                                              Bacteriophage lambda is assembled from preformed viral c
158                               Terminase from bacteriophage lambda is composed of gpA (72.4 kDa) and g
159                    The terminase enzyme from bacteriophage lambda is composed of two viral proteins (
160                       The lysogenic state of bacteriophage lambda is exceptionally stable yet the pro
161                        The prophage state of bacteriophage lambda is extremely stable and is maintain
162                       The lysogenic state of bacteriophage lambda is maintained by CI repressor, whic
163                                              Bacteriophage lambda is one of the most exhaustively stu
164                                              Bacteriophage lambda is one of the most extensively stud
165                             The cosQ site of bacteriophage lambda is required for DNA packaging termi
166                    The terminase enzyme from bacteriophage lambda is responsible for excision of a si
167                    The terminase enzyme from bacteriophage lambda is responsible for the insertion of
168                    The terminase enzyme from bacteriophage lambda is responsible for the insertion of
169 in the early part of the late gene operon of bacteriophage lambda is subject to such cleavage and res
170             The integrase protein (Int) from bacteriophage lambda is the archetypal member of the tyr
171           The excisionase (Xis) protein from bacteriophage lambda is the best characterized member of
172           A critical step in the assembly of bacteriophage lambda is the excision of a single genome
173  an enzyme encoded by the Nu1 and A genes of bacteriophage lambda, is crucial for packaging concateme
174 he bacterium Escherichia coli and its virus, bacteriophage lambda, is paradigmatic for gene regulatio
175 sitive control" mutants of the cI protein of bacteriophage lambda (lambda cI) bind DNA but, unlike th
176           The protein phosphatase encoded by bacteriophage lambda (lambda PP) belongs to a family of
177          We also show that SarA binds to the bacteriophage lambda (lambda) attachment site, attL, pro
178                                              Bacteriophage lambda (lambda) permits the display of man
179                                          The bacteriophage lambda (lambda) recombination system Red h
180 sical and functional characterization of the bacteriophage lambda (lambda) scaffolding protein gpNu3.
181     The site-specific recombinase encoded by bacteriophage lambda [lambda Integrase (Int)] is respons
182                            The cI protein of bacteriophage lambda (lambdacI) activates transcription
183                            The cI protein of bacteriophage lambda (lambdacI) activates transcription
184                             The Q protein of bacteriophage lambda (lambdaQ) is a transcription anti-t
185 the filtrates of M. tuberculosis cultures, a bacteriophage lambda library of M. tuberculosis H37Rv DN
186                          Upon induction of a bacteriophage lambda lysogen, a site-specific recombinat
187 ent phenanthriplatin on Escherichia coli and bacteriophage lambda lysogens is reported.
188                                              Bacteriophage lambda makes two proteins with overlapping
189                     The integrase protein of bacteriophage lambda mediates recombination via four dis
190 es to survey the roles of P-loop residues in bacteriophage lambda motor function.
191                                              Bacteriophage lambda moves its viral genome into and out
192                                              Bacteriophage lambda N and bacterial Nus proteins togeth
193  enhanced affinity and specificity using the bacteriophage lambda N peptide-boxB interaction as a mod
194         Transcription antitermination by the bacteriophage lambda N protein is stimulated in vitro by
195                                          The bacteriophage lambda N protein reduces transcriptional s
196 orter system based on antitermination by the bacteriophage lambda N protein, it has been possible to
197  does not extend to another ClpXP substrate, bacteriophage lambda O protein, suggesting that RssB act
198 e-specific DNA-binding proteins, such as the bacteriophage lambda O replication initiator or the E. c
199                                              Bacteriophage lambda of Escherichia coli has two alterna
200  mutations in the large terminase subunit in bacteriophage lambda on packaging motor dynamics.
201              The effects of Kil peptide from bacteriophage lambda on the assembly of Escherichia coli
202 d cosmid vector pLorist6Xh, which contains a bacteriophage lambda origin of replication for low-copy-
203 ein, which is critical for lysogenization by bacteriophage lambda, overlaps the -35 region of the P(R
204                                          The bacteriophage lambda P and Escherichia coli DnaC protein
205 cles in the lysogeny maintenance promoter of bacteriophage lambda, P(RM).
206                              N proteins from bacteriophages lambda, P22, and phi21 modulate transcrip
207  containing the major Xis binding sites from bacteriophages lambda, P22, L5, HP1, and P2 and the conj
208  Rapid ejection of a 0.3(+) T7 genome from a bacteriophage lambda particle results in degradation of
209 lophosphoesterase superfamily exemplified by bacteriophage lambda phosphatase (lambda-Pase).
210 metallo-phosphoesterase fold (exemplified by bacteriophage lambda phosphatase) embellished by distinc
211                                              Bacteriophage lambda phosphoprotein phosphatase (lambdaP
212 formed on initiation complexes formed on the bacteriophage lambda PR promoter.
213  relief of TI by CI or Cro repressors in the bacteriophage lambda PR-PRE system show strong relief of
214                            beta protein from bacteriophage lambda promotes a single-strand annealing
215 te-specific recombinase integrase encoded by bacteriophage lambda promotes integration and excision o
216                                              Bacteriophage lambda protein phosphatase (lambdaPP) is a
217                                              Bacteriophage lambda protein phosphatase (lambdaPP) is a
218                                              Bacteriophage lambda protein phosphatase (lambdaPP) with
219                            Reconstitution of bacteriophage lambda protein phosphatase in the presence
220                                              Bacteriophage lambda protein phosphatase is also conside
221                           The interaction of bacteriophage lambda protein phosphatase with Mn2+ was s
222  an asymmetrical folding transition state of bacteriophage lambda protein W, which has yet to be subj
223 ion of natural biological machinery, such as bacteriophage lambda proteins for recombineering and CRI
224  4/beta-flap interaction is required for the bacteriophage lambda Q antiterminator protein (lambdaQ)
225 main of the beta subunit is required for the bacteriophage lambda Q antiterminator protein to contact
226                                              Bacteriophage lambda Q-protein stably binds and modifies
227                                          The bacteriophage lambda recombination system has proven to
228 ar mechanistic differences between Tn916 and bacteriophage lambda recombination.
229 hat process the recombining oligo and affect bacteriophage lambda Red-mediated oligo recombination.
230                                Here, we used bacteriophage lambda Red-mediated recombination, or "rec
231         The system utilizes the well defined bacteriophage lambda regulatory circuit where the viral
232                                          The bacteriophage lambda relies on interactions of the cI an
233                                              Bacteriophage lambda repressor activates transcription f
234                                          The bacteriophage lambda repressor and its relatives bind co
235 MalK was also demonstrated in vivo using the bacteriophage lambda repressor fusion assay.
236 lcB polypeptide to the DNA-binding domain of bacteriophage lambda repressor leads to the formation of
237 s used to measure the oligomerization of the bacteriophage lambda repressor protein at micromolar con
238                    Our data show that unlike bacteriophage lambda, repressor bound at O(L) of bacteri
239 stigated the binding interaction between the bacteriophage lambda-repressor CI and its target DNA usi
240  Under usual laboratory conditions, lysis by bacteriophage lambda requires only the holin and endolys
241  recently been identified as the factor from bacteriophage lambda responsible for the inhibition of b
242 hia coli with the red recombination genes of bacteriophage lambda results in a strain in which adapti
243                                              Bacteriophage lambda's N-protein includes a 17-amino-aci
244 ouble-stranded DNA from the Escherichia coli bacteriophage lambda served as the model DNA in our expe
245                            The life cycle of bacteriophage lambda serves as a simplified paradigm for
246 manner similar to the excisionase protein of bacteriophage lambda, serving an architectural role in t
247                                          The bacteriophage lambda site-specific recombinase (Int), in
248 n Fis was previously shown to be involved in bacteriophage lambda site-specific recombination in vivo
249                                              Bacteriophage lambda site-specific recombination is cata
250                                              Bacteriophage lambda site-specific recombination require
251 ing of target sequences by making use of the bacteriophage lambda site-specific recombination system.
252                                              Bacteriophage lambda stably maintains its dormant propha
253                          Several features of bacteriophage lambda suit it for the study of genetic re
254                                    Thus, the bacteriophage lambda surface display is powerful for iso
255                                              Bacteriophage lambda surface display was used to isolate
256                                            A bacteriophage lambda surface expression system, lambda f
257 und in specialized gene circuits such as the bacteriophage lambda switch and the Cyanobacteria circad
258 argeting various positions in the genomes of bacteriophages lambda, T5, T7, T4 and R1-37 and investig
259                 Using fluorescently labelled bacteriophage lambda tails, we quantitatively described
260 lu179 serves as the catalytic carboxylate in bacteriophage lambda terminase and probe its mechanistic
261                                              Bacteriophage lambda terminase holoenzyme is a hetero-ol
262                                              Bacteriophage lambda terminase is composed of two subuni
263                                              Bacteriophage lambda terminase possesses a site-specific
264                  The DNA packaging enzyme of bacteriophage lambda, terminase, is a heteromultimer com
265                                              Bacteriophage lambda-terminase, which serves as a protot
266                  Terminase is an enzyme from bacteriophage lambda that is required for insertion of t
267 component of the Red recombination system of bacteriophage lambda that promotes a single strand annea
268                                           In bacteriophage lambda the catalytic terminase subunit is
269                                           In bacteriophage lambda, the DNA recognition protein is gpN
270                    In the particular case of bacteriophage lambda, the ejection is 50% inhibited by o
271                                           In bacteriophage lambda, the overlapping open reading frame
272                                           In bacteriophage lambda, this frameshift controls productio
273  coli, this pathway confers immunity against bacteriophage lambda through an abortive infection mecha
274 l-characterized (lambda)Xis excisionase from bacteriophage lambda, Tn916Xis stimulates excision in vi
275 mbinant plasmid, as judged by the ability of bacteriophage lambda to form plaques, indicating that th
276 newly replicated chromosomes, and is used by bacteriophage lambda to integrate or excise its genome i
277 elting, and variants of the P(R) promoter of bacteriophage lambda to model the closed complex interme
278 ing of 'decoration' proteins (such as gpD in bacteriophage lambda) to the viral shell.
279 e in terminating transcripts in vitro at the bacteriophage lambda tR1 terminator and had correspondin
280                                          The bacteriophage lambda tR1 terminator encodes a region of
281 xpress the HBV X protein (HBx) and possess a bacteriophage lambda transgene to evaluate the in vivo e
282 ansgenic mice that express HBx and possess a bacteriophage lambda transgene were sacrificed at 30, 90
283 at both express HBx (ATX mice) and possess a bacteriophage lambda transgene with the hepatocarcinogen
284 en evaluated by genetic footprinting using a bacteriophage lambda transposon delivery system.
285 fic recombination reactions catalyzed by the bacteriophage lambda tyrosine recombinase integrase (Int
286                                              Bacteriophage lambda uses a holin-endolysin system for h
287  transcription antiterminator N protein from bacteriophage lambda uses its arginine-rich motif to spe
288                                              Bacteriophage lambda uses site-specific recombination to
289 nsgenic fish that carry multiple copies of a bacteriophage lambda vector that harbors the cII gene as
290  SSA utilizes tagged retroviral libraries in bacteriophage lambda vectors (retrophages).
291 igenic structures in aqueous preparations of bacteriophage lambda, Venezuelan equine encephalitis vir
292 ightly regulated pathway for the excision of bacteriophage lambda viral DNA out of the E. coli host c
293           The attachment site (attlambda) of bacteriophage lambda was examined in wild strains of Esc
294                              The rap gene of bacteriophage lambda was placed in the chromosome of an
295  pressure on the extent of DNA ejection from bacteriophage-lambda was recently investigated.
296                                          For bacteriophage lambda, we establish a mean ejection time
297 ool in 1964, and to study gene regulation in bacteriophage lambda when I was there.
298  was found by measuring the size spectrum of bacteriophage lambda, which has a noncontractile tail.
299 F) is a protein that binds to the H' site of bacteriophage lambda with sequence specificity.
300 hich a whole genome library is cloned into a bacteriophage lambda ZAP Express vector which contains b

 
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