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1     Its antibacterial activity is limited to gram positive bacteria.
2 ase probe in B. subtilis and closely related gram positive bacteria.
3 bility in a wider range of Gram negative and Gram positive bacteria.
4  covalently attached to the peptidoglycan of gram positive bacteria.
5 ss regulator Spx is ubiquitously found among Gram-positive bacteria.
6  elements are now thought to occur widely in gram-positive bacteria.
7 elevant for the killing of Gram-negative and Gram-positive bacteria.
8 tic with rapid bactericidal activity against gram-positive bacteria.
9 yclic depsipeptide antibiotic active against Gram-positive bacteria.
10 , but they are ineffective against resistant gram-positive bacteria.
11 est basins displayed an increase in only the gram-positive bacteria.
12 nst fluoroquinolone resistant MRSA and other Gram-positive bacteria.
13  cell wall biosynthesis and pathogenicity in Gram-positive bacteria.
14 le is known about flagellin glycosylation in Gram-positive bacteria.
15 tibiotics, which inhibit the growth of other Gram-positive bacteria.
16 ins to the peptidoglycan of the cell wall of gram-positive bacteria.
17 y key roles in several cellular processes in Gram-positive bacteria.
18 nctionalize the peptidoglycan layers of many Gram-positive bacteria.
19 ed in PHPT homologues from Gram-negative and Gram-positive bacteria.
20 ons caused by Staphylococcus aureus or other Gram-positive bacteria.
21 ning a new mechanism of protein anchoring in Gram-positive bacteria.
22 h regulates many amino acid-related genes in Gram-positive bacteria.
23 s and is known to possess selectivity toward Gram-positive bacteria.
24 e essential for function and conserved among Gram-positive bacteria.
25 ) is an important cell wall polymer found in gram-positive bacteria.
26  broad scope of activities against different Gram-positive bacteria.
27 nent required for proper cell growth in many Gram-positive bacteria.
28 es level differentiation of the investigated Gram-positive bacteria.
29 copeptide with bactericidal activity against gram-positive bacteria.
30 enuate the inflammatory responses induced by Gram-positive bacteria.
31 crobial activity against S. aureus and other Gram-positive bacteria.
32 conditions and many preferentially targeting Gram-positive bacteria.
33 to catalyze both reactions of the process in Gram-positive bacteria.
34 and subsequent release of vesicular cargo in Gram-positive bacteria.
35 ster units that are found in the envelope of Gram-positive bacteria.
36 ntier that has been investigated in only few Gram-positive bacteria.
37  secretion systems in many Gram-negative and Gram-positive bacteria.
38 (LTA) is an important cell wall component of Gram-positive bacteria.
39 e editing in lactic acid bacteria, and other Gram-positive bacteria.
40 is induced by STAT3 signaling in response to Gram-positive bacteria.
41 les were effective against gram-negative and gram-positive bacteria.
42 omplementing the method's proven utility for Gram-positive bacteria.
43 tative antimicrobial activity mainly against Gram-positive bacteria.
44 hrough amelioration of the disease burden of gram-positive bacteria.
45 s antimicrobial activity and selectivity for Gram-positive bacteria.
46 nvolved in protein quality control in low-GC Gram-positive bacteria.
47 rom positive blood culture broths containing Gram-positive bacteria.
48 .3% for Gram-negative bacteria and 98.3% for Gram-positive bacteria.
49 hila model of infection when cocultured with Gram-positive bacteria.
50 ring elongation in rod-shaped and ovococcoid Gram-positive bacteria.
51  occurs at spatially restricted foci in some Gram-positive bacteria.
52 ited potent antimicrobial properties against Gram-positive bacteria.
53 reaction that is essential for the growth of gram-positive bacteria.
54 by multiple lantibiotics produced by diverse Gram-positive bacteria.
55 ence proteins have so far been restricted to Gram-positive bacteria.
56 P family (for Rap, NprR, PrgX, and PlcR), in Gram-positive bacteria.
57 ays enhanced virulence during coculture with Gram-positive bacteria.
58  in Siphoviridae infecting a wide variety of Gram-positive bacteria.
59  genes) in a large group of phages infecting Gram-positive bacteria.
60 tive matrix - the first such observation for Gram-positive bacteria.
61 ll components such as lipoteichoic acid from Gram-positive bacteria.
62 eux, Inc.) for the identification of aerobic Gram-positive bacteria.
63 of a detrimental outcome from pneumonia with Gram-positive bacteria.
64  teichoic acid (WTA) to the peptidoglycan of Gram-positive bacteria.
65  represent a novel type of oxidoreductase in Gram-positive bacteria.
66 rowth inhibitory effect in Gram-negative and Gram-positive bacteria.
67 ins play a crucial role in virulence in some gram-positive bacteria.
68  whose hosts are Bacillus cereus and related Gram-positive bacteria.
69 dable in vitro activity against a variety of Gram-positive bacteria.
70 oups by their hosts, either Gram-negative or Gram-positive bacteria.
71 xhibits potent antimicrobial effects against Gram-positive bacteria.
72 iscuous plasmids and their preference toward Gram-positive bacteria.
73 tial target for evaluating antimicrobials in gram-positive bacteria.
74 anding the biology of tectiviruses infecting Gram-positive bacteria.
75 hat displays nanomolar activity against many Gram-positive bacteria.
76 e opposite trend was observed in the case of Gram-positive bacteria.
77 vidin, recognizing almost none of the tested Gram-positive bacteria.
78 obal regulator of transcription in low G + C Gram-positive bacteria.
79 wn function that is well conserved in low-GC Gram-positive bacteria.
80 he CTC protein, a feature typical to various Gram-positive bacteria.
81 ive peptide/protein pairs we engineered from Gram-positive bacteria.
82 wn tropism of RNA bacteriophages may include gram-positive bacteria.
83 nificant antimicrobial effect, especially in gram-positive bacteria.
84 uses (bacteriophages) specifically infecting Gram-positive bacteria.
85 izes many types of PAMPs that originate from gram-positive bacteria.
86  peptides, and vulnerability to infection by Gram-positive bacteria.
87 epeat glycoproteins (SRRPs) are conserved in Gram-positive bacteria.
88 ich is linked to cell growth and division in Gram-positive bacteria.
89 , Staphylococci, and Streptococci, and other Gram-positive bacteria.
90 ates initiation of DNA replication in low-GC Gram-positive bacteria.
91  The most commonly identified organisms were gram-positive bacteria.
92 negative bacteria, but neither is present in Gram-positive bacteria.
93 gh which the stringent response functions in Gram-positive bacteria.
94 ossessed weak antibacterial activity against Gram-positive bacteria.
95                   All bacteria detected were gram-positive bacteria (100%), most commonly: Staphyloco
96 fective drug target for resistant strains of Gram-positive bacteria.2 In addition, because sortase A
97                           Pathogens included Gram-positive bacteria (41%), Gram-negative bacteria (41
98             The most frequent pathogens were gram-positive bacteria (91.3%), including coagulase-nega
99                                 Furthermore, Gram-positive bacteria acutely activate Hippo-Yorkie sig
100     16S rRNA gene pyrosequencing showed that Gram-positive bacteria affiliated with the Firmicutes an
101 ting the translocation of selected arrays of Gram-positive bacteria against which the host mounts eff
102 or of coproporphyrinogen oxidase (CgoX) from Gram-positive bacteria, an enzyme essential for heme bio
103 tase, a cysteine-transpeptidase conserved in Gram-positive bacteria, anchors on the cell wall many su
104  representative of monomeric RmlD enzymes in Gram-positive bacteria and a subset of Gram-negative bac
105                    It is highly conserved in Gram-positive bacteria and controls transcription on a g
106  the formation of competence-induced pili in Gram-positive bacteria and corroborate the remarkable st
107 n a synthetic community of Gram-negative and Gram-positive bacteria and fungi.
108 s the Toll pathway responds predominantly to Gram-positive bacteria and fungi.
109 biosensors for in vivo metabolite imaging in Gram-positive bacteria and have validated the first dinu
110 translocons, found in both gram-negative and gram-positive bacteria and in some archaea.
111          GpsB protein is conserved in low-GC Gram-positive bacteria and is not essential in rod-shape
112  is present in a subset of gram-negative and gram-positive bacteria and is the founding member of a n
113 uld be used for the quantitative analysis of Gram-positive bacteria and might be applied potentially
114 inhibited the growth of antibiotic-resistant gram-positive bacteria and prolonged the survival of mic
115  youngest basins had increased abundances of gram-positive bacteria and saprotrophic fungi at higher
116 us of Zg16(-/-) animals had a higher load of Gram-positive bacteria and showed bacteria with higher m
117 rganisms (like plants and cyanobacteria), in Gram-positive bacteria, and a few other bacterial phyla.
118 is a recently identified endoribonuclease in Gram-positive bacteria, and an RNase Y ortholog has been
119 e reductase) protein family, is conserved in Gram-positive bacteria, and interacts with RNA polymeras
120 es an overview of RNA-mediated regulation in Gram-positive bacteria, and is highlighted with specific
121                                           In Gram-positive bacteria, and particularly the Firmicutes,
122 gram-negative bacteria, lipoteichoic acid in gram-positive bacteria, and phospholipomannan in fungi.
123 served yet uncharacterized proteins found in Gram-positive bacteria, and they shed new light on the r
124 protein family, which is spread widely among gram-positive bacteria; and suggests approaches to targe
125 gram-negative bacteria, infections caused by gram-positive bacteria, antimicrobial stewardship and in
126                                              Gram positive bacteria are the major contributor of bact
127                                              Gram-positive bacteria are decorated by a variety of pro
128             The peptidoglycan layers of many gram-positive bacteria are densely functionalized with a
129 ng adhesive matrix molecules (MSCRAMMs) from Gram-positive bacteria are established virulence factors
130                          Surface proteins in Gram-positive bacteria are incorporated into the cell wa
131             Many amino acid-related genes in Gram-positive bacteria are regulated by the T box ribosw
132   However, the mechanisms of MV formation in Gram-positive bacteria are unclear, as these cells posse
133 obacteria and Firmicutes (high-GC and low-GC Gram-positive bacteria) are unable to synthesize protopo
134 on, P. aeruginosa uses peptidoglycan shed by Gram-positive bacteria as a cue to stimulate production
135 anscription in innate immunity, and identify Gram-positive bacteria as extracellular stimuli of Hippo
136                                              Gram-positive bacteria as well as their cell wall compon
137 ver, treated cattle had reduced abundance of gram-positive bacteria at the genus level.
138 n shows broad antibacterial activity against Gram-positive bacteria, but is also hemolytic and cytoto
139 ions and is evolutionarily conserved in many Gram-positive bacteria, but its function in M. tuberculo
140 er regulator of carbon source utilization in gram-positive bacteria, but the CcpA regulon remains ill
141           It permeates the cell membranes of Gram-positive bacteria by binding to the cell wall precu
142 ium conditions for optimal identification of Gram-positive bacteria by use of MALDI-TOF MS.
143                                              Gram-positive bacteria cause a broad spectrum of infecti
144                             A broad range of gram-positive bacteria cause serious infections in the c
145                                              Gram-positive bacteria cause the majority of skin and so
146      The serine-rich repeat glycoproteins of Gram-positive bacteria comprise a large family of cell w
147 al functions of specific compounds, and that Gram-positive bacteria considered to be obligate aerobes
148 oteichoic acid (LTA), a cell wall polymer of gram-positive bacteria, consists of 1,3-polyglycerol-pho
149                             The cell wall of Gram-positive bacteria contains abundant surface-exposed
150                        The cell wall of most Gram-positive bacteria contains equal amounts of peptido
151                                         Many Gram-positive bacteria coordinate cellular processes by
152                                           In Gram-positive bacteria, CPS linkage is to either the cyt
153  the B16-OVA melanoma model and an optimized Gram-positive bacteria-dendritic cell (DC) vaccination s
154                        The virulence of many Gram-positive bacteria depends on cholesterol-dependent
155 th antibiotics that target Gram-negative and Gram-positive bacteria develop ameliorated psoriasiform
156  call NDA-1, contributes to the reduction of Gram-positive bacteria during early development and thus
157                                      In some gram-positive bacteria (e.g. Staphylococcus aureus), sor
158 ies have shown that ADEPs are active against Gram-positive bacteria (e.g., MRSA, VRE, PRSP (penicilli
159 polyisoprenoid biosynthesis, is essential in Gram-positive bacteria (e.g., Staphylococcus, Streptococ
160 itory concentration (MIC) was much lower for Gram positive bacteria (Enterococcus spp. and Staphyloco
161                             However, in many Gram-positive bacteria, especially in fermicutes, RNAP i
162 oronate chemistry allows potent labelling of Gram-positive bacteria even in the presence of 10% serum
163                                           In Gram-positive bacteria, extracellular protein appendages
164 e to certain members of the low-G+C group of Gram-positive bacteria (Firmicutes) and requires signatu
165 amined PrsA proteins encoded by a variety of Gram-positive bacteria for functional complementation of
166 rgest inhibition zones were observed against Gram-positive bacteria for halloysite samples.
167 ased on self-assembly of vancomycin (Van) on Gram-positive bacteria for imaging bacterial infection.
168 doxin reductase, a protein essential in many Gram-positive bacteria for maintaining the thiol-redox b
169 ., Northbrook, IL) for the identification of Gram-positive bacteria from blood cultures.
170 ficiently removes multiple Gram-negative and Gram-positive bacteria, fungi and endotoxins from whole
171  peptide sensor to various concentrations of Gram-positive bacteria generated reproducible impedance
172                                   Given that Gram-positive bacteria genomes encode a variety of sorta
173 ding Eukaryota, Homo sapiens, Viridiplantae, Gram-positive Bacteria, Gram-negative Bacteria and Virus
174 numerous antibiotic resistance plasmids from Gram-positive bacteria, Gram-negative phage and the mobi
175 erpretation of such results, especially when gram-positive bacteria grow.
176 e ppk and ppx genes, none of the spores from Gram-positive bacteria had granules.
177 though riboflavin precursor derivatives from Gram-positive bacteria have been characterized, some lev
178                Regulators of PBP activity in Gram-positive bacteria have yet to be discovered but are
179 ickness can vary greatly among species, with Gram-positive bacteria having a thicker wall than Gram-n
180                           The highest ranked Gram-positive bacteria (high priority) were vancomycin-r
181 iotic resistance in bacteria have focused on Gram-positive bacteria; however, multidrug-resistant Gra
182 ctivation is correlated with the presence of Gram-positive bacteria in carious human teeth.
183 nsor device to efficiently detect pathogenic Gram-positive bacteria in food samples.
184                              The presence of Gram-positive bacteria in foodstuffs is a chronic worldw
185 Mycobacterium tuberculosis, are unique among Gram-positive bacteria in producing a complex cell wall
186 hydrochalcones are able to inhibit growth of Gram positive bacteria, in particular Staphylococcus aur
187 a in the phylum Firmicutes (formerly low-G+C Gram-positive bacteria) includes diverse bacteria of med
188  antibiotic with activity against a range of Gram-positive bacteria including drug-resistant pathogen
189    The lantibiotic NAI-107 is active against Gram-positive bacteria including vancomycin-resistant en
190 found that auranofin is active against other Gram-positive bacteria, including Bacillus subtilis and
191  shown to play a role in the pathogenesis of Gram-positive bacteria, including E. faecium We previous
192 psin was bactericidal against a diversity of Gram-positive bacteria, including human pathogens such a
193 aining domains are unexpectedly prevalent in Gram-positive bacteria, including many clinically releva
194 crobial activity against multidrug-resistant Gram-positive bacteria, including MRSA and VRE, rapid ti
195   The obtained compounds were active against Gram-positive bacteria, including multiresistant Staphyl
196                                         Many Gram-positive bacteria, including the human pathogen Lis
197 ial activity against model Gram negative and Gram positive bacteria is reported for selected compound
198            We conclude that PGN derived from gram-positive bacteria is a potent platelet agonist when
199 at cyclic-di-adenosine monophosphate in live Gram-positive bacteria is a vita-PAMP, engaging the inna
200             The peptidoglycan that surrounds Gram-positive bacteria is affixed with a range of macrom
201 c IgG booster responses to Gram-negative and Gram-positive bacteria is contained solely within the B
202   Surface display of proteins by sortases in Gram-positive bacteria is crucial for bacterial fitness
203                     Vancomycin resistance in Gram-positive bacteria is due to production of cell-wall
204   However, iron-sulfur cluster biogenesis in Gram-positive bacteria is not so well characterized, and
205  that acidification of phagosomes containing Gram-positive bacteria is regulated by the NLRP3 inflamm
206 or example, increasing drug resistance among gram-positive bacteria is responsible for approximately
207        Inflammation caused by infection with Gram-positive bacteria is typically initiated by interac
208      The mechanism of persister formation in Gram-positive bacteria is unknown.
209 d cell shape, and, in the case of pathogenic Gram-positive bacteria, it lies at the interface between
210             By contrast, Ntox28 domains from Gram-positive bacteria lack C-terminal Gly-Tyr-Gly-Ile m
211             Export of cell surface pilins in Gram-positive bacteria likely occurs by the translocatio
212  in mechanism of action on gram-negative and gram-positive bacteria may be less pronounced than forme
213 oteins not linked to a pilus gene cluster in Gram-positive bacteria may hijack the pilus.
214     Furthermore, the pilus shaft assembly in Gram-positive bacteria may require a tip, as is true for
215 elated wall-associated protein A (WapA) from Gram-positive bacteria mediate intercellular competition
216 uggest that therapeutic strategies targeting Gram-positive bacteria might be a viable approach for re
217                                        Among Gram-positive bacteria, mortality was highest for methic
218 t activity and antibacterial effects against Gram-positive bacteria, namely methicillin-susceptible S
219 1,157) of single-organism cultures contained Gram-positive bacteria not present on the BC-GP test pan
220 sensitive and resistant Gram-negative and/or Gram-positive bacteria of new amphiphilic 3',4'-dialkyl
221                                The impact of gram-positive bacteria on the innate and adaptive respon
222                         In contrast to other Gram-positive bacteria, only one single sortase enzyme,
223     Little is known about their formation in Gram-positive bacteria, particularly among facultative a
224                                              Gram-positive bacteria, particularly coagulase-negative
225                                           In Gram-positive bacteria, PCATs function both as maturatio
226             The DnaB primosomal protein from Gram-positive bacteria plays a key role in DNA replicati
227                                  Most low GC Gram-positive bacteria possess an essential walKR two-co
228 and inhibits cell wall biosynthesis in other Gram-positive bacteria probably by binding to lipid II,
229 bernation promoting factor (HPF), while most Gram-positive bacteria produce a single, longer HPF prot
230 here enhances our understanding of how other Gram-positive bacteria produce essential components of t
231          However, recent work has shown that Gram-positive bacteria produce extracellular vesicles an
232                                         Many Gram-positive bacteria produce lantibiotics, genetically
233 role in CMP-pseudaminic acid biosynthesis in Gram-positive bacteria provides a foundation to investig
234 function are broadly conserved among diverse Gram-positive bacteria, PrsA2 exhibits unique specificit
235                  Antimicrobial resistance in gram-positive bacteria remains a challenge in infectious
236 of infections caused by antibiotic-resistant gram-positive bacteria requires the discovery of new dru
237  Type VII protein secretion system, found in Gram-positive bacteria, secretes small proteins, contain
238 are gene-regulatory mRNA elements with which Gram-positive bacteria sense amino acid availability.
239 basis for formation of the 100S complexes in Gram-positive bacteria, shedding light on the mechanism
240 al strains, including both Gram-negative and Gram-positive bacteria, showing great potential for appl
241 cond messenger predicted to be widespread in Gram-positive bacteria, some Gram-negative bacteria, and
242                                           In Gram-positive bacteria, sortase-dependent pili mediate t
243 /mL against representative Gram-negative and Gram-positive bacteria species.
244  rhinosinusitis (CRS) has been linked to the gram-positive bacteria Staphylococcus aureus (S. aureus)
245             They showed activity against two Gram-positive bacteria Staphylococcus aureus and Enteroc
246  cytokine mRNA expression in response to the Gram-positive bacteria Streptococcus pneumoniae and Stap
247 antibacterial properties, especially against Gram-positive bacteria such as S. aureus.
248  of complement by FH6-7/Fc on the surface of Gram-positive bacteria such as S. pyogenes will enable p
249        It is clinically used against various Gram-positive bacteria such as Staphylococcus aureus and
250 oro derivative that retains activity against Gram-positive bacteria, such as anthrax, but also shows
251                           Pheromones of many gram-positive bacteria, such as Bacillus and Streptococc
252 s exhibited antibacterial activities against gram-positive bacteria, such as Bacillus subtilis and St
253                                     In other gram-positive bacteria, such as Enterococcus faecalis, d
254 ied in multiple pilus gene clusters of other Gram-positive bacteria, suggesting that similar signalin
255                                              Gram-positive bacteria surround themselves with a thick
256                                           In Gram-positive bacteria, T-box riboswitches regulate the
257 Nocardia exalbida, all the other 725 (99.7%) gram-positive bacteria tested were susceptible to vancom
258                 They are more active against Gram positive bacteria than Gram negative bacteria; howe
259        shCD6 can bind to a broad spectrum of gram-positive bacteria thanks to the recognition of high
260 treptococcus agalactiae) are beta-hemolytic, Gram-positive bacteria that are common asymptomatic colo
261 TA) is a major component of the cell wall of Gram-positive bacteria that can trigger inflammatory res
262  Streptococcus agalactiae are beta-hemolytic gram-positive bacteria that colonize the lower genital t
263 enzyme superfamily are widely distributed in Gram-positive bacteria that frequently utilize multiple
264                 Actinomycetes are a group of gram-positive bacteria that includes pathogenic mycobact
265 ied by sequence similarity in the genomes of Gram-positive bacteria that possess IsdG-family heme oxy
266 Bacilli are ubiquitous low G+C environmental Gram-positive bacteria that produce a wide assortment of
267  environmental conditions, including, within Gram-positive bacteria, the stressosome complex that reg
268 tibody-conjugated AuNPs can readily identify Gram-positive bacteria through antibody-antigen recognit
269 ns that mediate the attachment of pathogenic Gram-positive bacteria to host cells.
270 rticles (AuNP) modified with monoclonal anti-Gram-positive bacteria to produce an immune-sensor.
271 iffuse more easily into porous cell walls of Gram-positive bacteria to reach sensitive sites, while t
272 face protein repeats involved in adhesion of Gram-positive bacteria to the intestine.
273  The more penetrable Zg16(-/-) mucus allowed Gram-positive bacteria to translocate to systemic tissue
274 activated platelets and mediates adhesion of Gram-positive bacteria to various host cells.
275                                              Gram-positive bacteria typically use small peptides as Q
276                            Gram-negative and gram-positive bacteria use a variety of enzymatic pathwa
277                                              Gram-positive bacteria use reactive thioester-containing
278                                     However, Gram-positive bacteria utilize an acyltransferase pathwa
279                 ZG16 bound to and aggregated Gram-positive bacteria via binding to the bacterial cell
280                                    Unique to Gram-positive bacteria, wall teichoic acids are anionic
281      The Biomic category agreement for 5,233 Gram-positive bacteria was 98.7%, with 0.9% minor, 0.3%
282 viously, extracellular vesicle production in Gram-positive bacteria was dismissed due to the absence
283 iation of the gene with heme biosynthesis in Gram-positive bacteria was previously demonstrated by ex
284         delta, a small protein found in most Gram-positive bacteria was, for a long time, thought to
285 ogy between MurJ and putative orthologs from Gram-positive bacteria, we explored the conservation of
286                            Gram-negative and Gram-positive bacteria were equally cultured.
287                                              Gram-positive bacteria were isolated in 78.5%; Staphyloc
288              1,252 blood cultures containing Gram-positive bacteria were prospectively collected and
289                                              Gram-positive bacteria were responsible for a high propo
290                                              Gram-positive bacteria were sensitive to vancomycin (27/
291  REDOX 1 40-ml aerobic bottles demonstrating Gram-positive bacteria were tested.
292 istributed among different gram-negative and gram-positive bacteria, where they act as pathogenicity
293 a extracts were more effective in inhibiting Gram-positive bacteria while soybean extract exhibited s
294 oncentrations in different Gram-negative and Gram-positive bacteria, while its hemolytic activity rem
295  These adhesives kill both Gram-negative and Gram-positive bacteria, while sparing human erythrocytes
296 glycopolymers found on the cell wall of many Gram-positive bacteria, whose diverse surface structures
297                           Promysalin acts on Gram-positive bacteria with a mechanism of action involv
298 pound also has high antibacterial potency on Gram-positive bacteria with an MIC versus wild type S. a
299           Real-time, label-free detection of Gram-positive bacteria with high selectivity and sensiti
300 edicine and nanotechnology.It is unclear how Gram-positive bacteria, with a thick cell wall, can rele

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