Development of [beta]-lactamase as a tool for monitoring conditional gene expression by a tetracycline-riboswitch in methanosarcina acetivorans.
Methanogenic Archaea, a monophyletic group of strictly anaerobic archaea, are responsible for the vast majority of biologically produced methane. The process, methanogenesis, is not only highly relevant for anthropocentric concerns, such as climate change, sustainable energy strategies, waste treatment, and agriculture but also plays an essential role in the global carbon cycle because it recycles organic matter from anaerobic to aerobic environments  (and references therein). Methanogens convert intermediates of anaerobic biomass degradation, like [H.sub.2]+C[O.sub.2], formate, acetate, and methylated compounds to methane via distinct yet overlapping pathways, and couple this process to energy conservation via a chemiosmotic mechanism [2,3]. In Methanosarcina species, methanogenesis from methylated compounds, such as methanol or methylamines, proceeds by transfer of the methyl-group to coenzyme M (CoM) via substrate-specific methyltransferases  and subsequent reduction of methylCoM to methane .
Methanogens comprise one of the few genetically tractable groups among the Archaea  and, thus, provide outstanding model organisms for the study of this so-called "third form of life." Despite the progress in developing tools for genetic manipulation of methanogens [7-9], many powerful techniques which are commonly applied in bacterial genetics have not yet been adapted for this group. For example, color screening of mutant libraries using [beta]-galactosidase (the lacZ gene product) and the substrate analog X-Gal (5-bromo-4-chloro-3-indolyl-[beta]-D-galactopyranoside) as a reporter system has been employed for decades in bacteria. In methanogens, both lacZ and uidA (encoding [beta]-glucuronidase from E. coli) can also be used as reporter genes [10, 11]. However, formation of the respective chromogenic cleavage product (indigo dye) requires the presence of oxygen. Thus, for color screening of methanogenic mutants on solid media, colonies have to be exposed to oxygen requiring either replica plating or a certain degree of tolerance towards oxygen [12, 13]. To obviate the requirement of exposing strictly anaerobic Methanosarcina to air, we report here on a color-screenable reporter gene system active in the absence of oxygen.
Regulable gene expression systems are also powerful genetic tools. Although a variety of such systems are available for methanogenic archaea, most of them involve the use of endogenous metabolic promoters and therefore change of cultivation conditions (e.g., switch of energy substrate or nitrogen source) is required to achieve induction or repression of transcription of the gene of interest [14-17]. The only exception so far is an artificial hybrid promoter making use of the transcriptional regulator TetR and the TetR binding site tetO, which are part of the Tn10-encoded system for tetracycline (tc) resistance in E. coli . By inserting TetR binding sites into the strong, constitutively expressing mcrB promoter (mcr[B.sub.P]), which controls the first gene of the mcrBCDGA operon encoding methyl-CoM reductase in M. barkeri , expression of genes under control of this hybrid promoter was tc-dependent in M. acetivorans,which is naturally tc-resistant . Therefore, to achieve tc-dependent gene regulation using this system, TetR has to be coexpressed.
Riboswitches are RNA-based regulatory elements, which control a plethora of metabolic genes in bacteria frequently found in the 5' untranslated region (UTR) of genes related to the metabolism or transport of the ligand they respond to. They are composed of an aptamer domain sensing the concentration of a cellular metabolite and an expression platform, which reads out the binding status of the aptamer domain switching gene expression ON or OFF . Riboswitches were previously only predicted bioinformatically for the Archaea [22,23]. Very recently, a fluoride-riboswitch was confirmed by genetic analysis in Thermococcus kodakarensis (T. J. Santangelo, personal communication). Synthetic riboswitches have been engineered for the conditional control of gene expression both in bacterial and eukaryal systems . Similar to their natural counterpart, they recognize a small molecule ligand via an aptamer domain with high affinity and specificity and control the expression of the gene they reside at the level of translation initiation, pre-mRNA splicing or mRNA stability. Their independence from protein factors as well as the abilityto raise synthetic binding domains (aptamers) against virtually any ligand of choice (a process called SELEX, [25,26]) led to the widespread implementation of RNA-based regulators as control devises in the field of synthetic biology .
The tc-binding aptamer has been employed as synthetic riboswitch in yeast for the conditional control of gene expression . It consists of three helices P1-P3, which are intercepted by single stranded regions. Multiple contacts between tc and nucleotides located in the single stranded regions result in an extremely tight binding constant in the pM range . Inserted in the 57UTR of an mRNA, the aptamer interferes with the scanning ribosome but only when its ligand is bound . Further, when the aptamer is inserted close to the 5' splice site of an intron it interferes in its ligand-bound form with splice site recognition, switching gene expression off . In this example, the most prominent regulation was obtained when the complete splice site was included within the closing stem of the aptamer. Breathing of the stem in the absence of ligand allows splicing and stabilization of the aptamer upon ligand binding prevents it, making the splice site inaccessible. In the present study, we have employed the tc-RS as synthetic riboswitch for conditional control of gene expression in M. acetivorans. By placing the tc-RS in various distances to the ribosome binding site of the downstream gene we could observe a dynamic range of regulation.
2. Materials and Methods
2.1. Bacterial Strains and Growth Conditions. E. coli was grown under standard conditions . M. acetivorans strains, listed in Table 1, were grown in high-salt medium as described . Either methanol (125 mM) or trimethylamine (50 mM) served as the energy source for growth. Solid medium contained 1.5% (w/v) Bacto agar (BD, Heidelberg). For selection of the puromycin transacetylase gene (pac), puromycin (CalBiochem, San Diego, CA) was added from sterile, anaerobic stocks at a final concentration of 2 [micro]gm[L.sup.-1]. The purine analog 8-aza-2,6-diaminopurine (Sigma, St. Louis, MO) was added from sterile, anaerobic stocks at a final concentration of 20 [micro]g m[L.sup.-1] for selection against the hypoxanthine phosphoribosyl transferase gene (hpt). Tc or doxycycline (dox) was added from sterile, anaerobic stocks at a final concentration of 200 [micro]M (or as indicated) when tc-RS-dependent bla translation was assessed. Growth of M. acetivorans was monitored photometrically at 578 nm ([OD.sub.578]).
2.2. Molecular Methods, Plasmid Construction and Transformation. Standard molecular methods were used for manipulation of plasmid DNA from E. coli . All plasmids used, except for pWM321, are nonreplicating in M. acetivorans and are listed in Table 1. Autonomous replication in (pWM321), or integration into the chromosome of M. acetivorans, was selected for with puromycin. The plasmid pMR56 for insertion into the hpt locus of M. acetivorans (by homologous recombination via a truncated allele) was generated by replacing the bla cassette (used for selection of ampicillin resistance in E. coli) of pAMG48 with the kanamycin resistance cassette from pET28a(+) (Novagen). The bla gene from E. coli encoded on pBR322 was amplified by PCR without the sequence for the signal peptide and cloned into pMR56, resulting in pBlaN. There, the bla gene is under control of mcr[B.sub.P] . A variant where bla is preceded by the putative signal peptide encoding sequence from the putative M. acetivorans flagellin MA3061 was also constructed and designated pBlaNFSP. Plasmid pMG3 was constructed by replacing mcr[B.sub.P] in pBlaNFSP by the ca. one kb sequence preceding mtaCl (MA0456), which encodes the corrinoid protein of the methanol-specific methyltransferase MT1 [35, 36]. To obtain plasmid pP0145NFSP, mcr[B.sub.P] in pBlaNFSP was replaced by the ca. one kb sequence preceding mtmCl (MA0145), which encodes the corrinoid protein of a monomethylamine-specific methyltransferase MT1 . pBlaN-prom was constructed by deletion of mcrBp to obtain a vector without [beta]-lactamase expression used as a negative control. For promoter deletion, pBlaN was digested with BglII and NdeI, blunted and religated.
The three tc-RS encoding plasmids pBlaN_tc-RS1, pBlaN_tc-RS3, and pBlaN_tc-RS5 were constructed via a crossover PCR procedure . In the first step, two asymmetric but overlapping PCR fragments were generated. pBlaN was used as template for fragment 1 encoding mcr[B.sub.p] without the ribosomal binding site (RBS) and the 5' end of the tc-RS. pSP64-tc-minimer  encoding the tc-aptamer was used for generation of fragment 2 containing the tc-RS with attached RBS. In the second step, the fragments were annealed at their overlapping region and amplified by PCR as a single fragment, using the outer primers of the first PCRs (primers pBlaN_fwd and either tc1_RBS_rev, tc2_RBS_rev, or tc3_RBS_rev, see the Supplementary Material available online at http://dx.doi.org/10.1155/2014/725610). The fragments were then cloned via BglII and NdeI into pBlaN. The other tc-RS encoding plasmids were also constructed via a crossover PCR procedure. The two overlapping PCR fragments spanning the sequence flanked by BglII and NdeI encoding the mcr[B.sub.P]-tc-RS-RBS fusion were generated from the precursor construct (tc-RS2 from tc-RS1, tc-RS4a from tc-RS3, and tc-RS4/4b from tc-RS4a), thereby introducing the desired nucleotide exchanges with the primers used (Supplementary Table S1).
Genomic DNA from M. acetivorans was isolated using a modified cetyl trimethylammonium bromide-NaCl method . Unmarked chromosomal insertions in M. acetivorans were confirmed by Southern hybridization  using a probe hybridizing with the bla gene. All DNA sequences obtained by PCR (primers are listed in Supplementary Table S1) were confirmed by sequencing at SRD (Bad Homburg, Germany) using the BigDye Terminator Cycle Sequencing protocol (Applied Biosystems, Foster City, USA). E. coli was transformed by electroporation . Liposome-mediated transformation of M. acetivorans was conducted as described , modified in  for markerless insertion of reporter constructs into the M. acetivorans genome .
2.3. Reporter Gene Product Activity. For qualitative detection of [beta]-lactamase (Bla) activity in cultures, cell lysates, or culture supernatants, nitrocefin (CalBiochem, San Diego, USA) was added from an anaerobic sterile 1 mM stock solution (prepared according to the manufacturer's instruction) to 20 [micro]M and incubated at room temperature for 10-30 min. Culture supernatants were prepared by centrifugation of cultures at 1,500 xg for 20 min and transfer of the supernatant into fresh anaerobic tubes. The cell sediment was lysed in deionized water (1/20 of the original culture volume) for 10 min and the lysate was brought to the volume of the original culture with high-salt medium to retain the same protein concentration as in the original culture. For Bla-dependent color development in/around colonies on agar plates, the nitrocefin stock was dispersed from a nasal spray container onto the plates after colonies of M. acetivorans had developed (nitrocefin is not stable for more than 2-3 h in HS medium). Cells did not loose viability by this treatment because colonies could be readily restreaked. For quantification of Bla in M. acetivorans, cells were harvested by centrifugation at [OD.sub.578] of 0.4-0.5 and osmotically lysed by addition of assay buffer (100 mM potassium phosphate buffer, 1mM EDTA, pH 7.0) containing 0.1 [micro]g m[L.sup.-1] DNasel. After 30 minincubationonice, the lysate was cleared by re-centrifugation. 50 [micro]L of the cleared lysate was added to 850 [micro]L assay buffer and equilibrated for 5 min at room temperature before the assay was started by adding 100 [micro]L of a 100 [micro]M nitrocefin solution. The initial rate of nitrocefin hydrolysis was recorded for 300 seconds at 486 nm and the specific Bla activity calculated using the molar extinction coefficient for nitrocefin ([[epsilon].sub.486] = 20,5 00 [M.sup.-1] [cm.sup.-1]). The values were corrected by subtracting those obtained for the strain carrying blaN without a promoter (pBlaN-prom), grown under the same conditions as the tc-RS-carrying strains. Protein concentration was determined by the method of Bradford  using bovine serum albumin as standard.
3. Results and Discussion
3.1. Synthesis and Secretion of Active [beta]-Lactamase in M. acetivorans. To establish in M. acetivorans a chromogenic reporter system not requiring oxygen for color development, the bla gene from E. coli was chosen because a chromogenic substrate for [beta]-lactamase, nitrocefin, is commercially available. Upon cleavage of the [beta]-lactam ring, it undergoes a distinctive color change from yellow ([I.sub.max] = 390 nm at pH 7.0) to red ([I.sub.max] = 486 nm at pH 7.0). Furthermore, Bla is a periplasmic protein in E. coli allowing its potential secretion from the cell, which could facilitate its detection. To avoid interference of a plasmid-borne selection marker used for cloning in E. coli with our analysis, the ampicillin resistance cassette was first replaced by a kanamycin resistance cassette. Thereby, the vector backbone would not need to be removed from the chromosome after integration into the M. acetivorans chromosome. Using this vector (pMR56) the bla gene, devoid of its natural signal peptide encoding sequence, was put under control of the strong constitutive methanoarchaeal mcr[B.sub.P] and placed onto the M. acetivorans chromosome (Figure 1(a)). As cleavage of an exogenous chromogenic Bla substrate and, thus, color development, would require either cell lysis or Bla excretion, a bla variant encoding a putative protein translocation signal peptide (from MA3061, pBlaNFSP) was also created and placed onto the M. acetivorans chromosome (Figure 1(a)). Both strains synthesized active Bla as evidenced by nitrocefin cleavage when cell lysates were assayed (Figure 1(b), "E"). While in the strain synthesizing Bla without a signal peptide (pBlaN) no nitrocefin cleavage was observed in the culture or the culture supernatant, color developed in the untreated culture and in spent medium when Bla contained an archaeal putative signal peptide (pBlaNFSP). Together, these data demonstrate that (i) Bla activity in M. acetivorans is sufficiently stable in high-salt medium to allow visual detection, that (ii) the amino acid sequence employed ((M)WNTFSKDEKGFTG) is a functional protein export signal in M. acetivorans, and that (iii) Bla of E. coli is translocated over the M. acetivorans cytoplasmic membrane in a functional form. Color development became visible after 1030 min of incubation. However, prolonged incubation (>3h) led to moderate color development in plain medium indicating abiotic cleavage of the [beta]-lactam of nitrocefin (data not shown), which is possibly due to the highly reducing conditions of the medium. Furthermore, overnight incubation led to complete loss of any color indicating that nitrocefin is hydrolyzed during this long incubation. Therefore, nitrocefin cannot be included in the medium during growth of the organism.
3.2. Growth Substrate-Dependent Synthesis of [beta]-Lactamase in M. acetivorans. To achieve growth substrate-dependent reporter synthesis in M. acetivorans, the strong constitutive mcr[B.sub.P] preceding bla was exchanged with mtaC[1.sub.P] (pMG3), which leads to high expression of the genes controlled by it in the presence of methanol , and with mtmC[1.sub.P] (p0145NFSP), which should lead to methylamine-dependent expression of the gene controlled by it. The plasmids were integrated into the M. acetivorans C2A chromosome and the resulting strains examined for Bla synthesis. Methanol- or methylamine-dependent synthesis and excretion of Bla could indeed be observed in liquid cultures of both strains (Figure 2(a)). When both strains were streaked on agar plates containing either of the growth substrates, only colonies of the strain harboring p0145NFSP clearly regulated bla expression (Figure 2(b)). The strain harboring pMG3 developed color under both conditions (Figure 2(b)), which is due to fact that in the agar, some energy source is present that is metabolized via the methanol utilization pathway  leading to induction of the methanol utilization machinery while growing on methylamine-containing agar plates. A plating procedure for growth of M. acetivorans on an agar-free surface, which involves filtration of cells onto nitrocellulose filters and incubating them on media-soaked filter paper, has been established  and would have to be used in conjunction with pMG3 to obtain colonies not producing Bla in the absence of methanol. Presently, five trans-acting factors, MsrA, MsrB, MsrC, MsrD, and MsrE, are known to regulate expression of the genes encoding three methanol-specific MT1 isoforms MtaCB1, MtaCB2, and MtaCB3 on the level of transcription initiation . The methanol-specific MT1 isoforms are also regulated at the posttranscriptional level  but the factor(s) involved are unknown. Transcriptome analyses demonstrated substrate-dependent regulation of mono-, di-, and trimethylamine-specific MT1 isoforms in M. mazei Go1, Methanococcoides burtonii, andM. acetivorans, Mtm [47-49], but factors involved are also not known. Thus, both fusion constructs presented herein will be suitable tools to identify factors affecting methanol- and methylamine-dependent regulation by random loss-of-function mutagenesis . Because the mtaC1P-fsp-bla fusion (pMG3) is expressed on agar lacking methanol, its use (at least under these conditions) will be restricted to identify mutants not expressing bla, that is, mutants that have lost (an) transcriptional activators) of mtaC1P-dependent expression. As for methylamine-dependent regulation, both negative and positive effectors of mtmC1P expression can be sought for using the mtmC[1.sub.P]-fspbla fusion (p0145NFsP) and standard agar media. Such efforts are underway in our laboratory and will be reported elsewhere.
Archaea, like bacteria, employ two pathways for protein translocation, the Sec and the Tat (twin arginine motif) pathway . While the substrates of the former are unfolded during the process, the latter translocates (at least partially) mature proteins. Since Bla from E. coli is a periplasmic protein and secreted via the Sec pathway, we tagged it with an N-terminal signal peptide from a putative flagellin encoded in the M. acetivorans genome (MA3061), assuming that it would be translocated by the corresponding pathway, despite the fact that the organism is nonmotile . In Methanococcus species, the N-terminal signal peptides of the preflagellins are cleaved off by the type IV prepilin peptidase FlaK during translocation over the membrane [52, 53]. Therefore, any protein susceptible to the Sec pathway could be produced and secreted from M. acetivorans (without the signal peptide), which could greatly facilitate purification efforts. For Archaea, such a system for protein overproduction combined with secretion has so far been established only in the hyperthermophilic Thermococcus kodakarensis .
3.3. Developing the tc-Responsive Riboswitch for Conditional Gene Expression in M. acetivorans. Regulation of mRNA translation by naturally occurring riboswitches has not been reported for Archaea. A tc-RS, when fused to a leaderless reporter mRNA in the halophilic archaeon Haloferax volcanii, totally inhibited translation even in the absence of tc, which was taken as evidence that it forms a too stable structure in the high-salt cytoplasm of that organism . To test whether tc-RS can be used in methanoarchaea as a means to control gene expression in cis (Figure 3(a)), its encoding sequence was inserted into mcr[B.sub.P] of the mcr[B.sub.P]-blaN fusion (pBlaN), immediately upstream of the RBS (Figure 3(b), tc-RS1), and the construct placed onto the M. acetivorans chromosome. Bla activity could now be used as a measure for tc-dependent translation of bla mRNA (Table 2). Compared to the control without tc-RS (pBlaN), bla mRNA translation in the absence of tc was increased by ca. 2.5-fold, which is not uncommon and probably due to increased mRNA stability in the presence of a structured RNA element at the 5' end of a bacterial mRNA . In the presence of tc, Bla activity was reduced by a factor of 2.6, indicating that the tc-bound aptamer interferes with translation of the bla mRNA, probably by sterical hindrance of the recognition of the RBS. This is similar to the regulation observed for pre-mRNA splicing by the same riboswitch 30]. There, the aptamer was inserted next to the 5' splice site. Regulation of splicing was strongly dependent on the distance of the aptamer from the splice site and the stability of the closing stem. The fact that best regulation of pre-mRNA splicing was obtained when the splice site was completely integrated within the closing stem  prompted us to successively move the RBS preceding bla into the closing stem of the tc-RS, giving rise to the constructs tc-RS2 to tc-RS5 with 2, 3, 4, and 6 nucleotides included, respectively (Figure 3(b)). The pairing bases were changed accordingly (Figure 3(b), marked in violet). Inclusion of the RBS into the closing stem by 1, 2, and 3 nucleotides (tc-RS1, tc-RS2, andtc-RS3) successively reduced Bla activity (104 [+ or -] 2, 71 [+ or -] 2 and 43 [+ or -] 5 mU [mg.sup.-1], resp.; see Table 2) indicating a generally somewhat diminished access of the ribosome to its binding site. Corroborating this notion was the observation made using tc-RS5 where the RBS was moved by six nucleotides into the closing stem of tc-RS, which almost completely abolished Bla activity (Table 2). Apparently, the RNA element completely blocked access of the ribosome from this construct. Furthermore, constructs tc-RS2 and tc-RS3 did not show an improved regulation compared to tc-RS1 (1.8- and 2.7-fold). Construct tc-RS4 with four nucleotides of the RBS within the closing stem was exceptional because it resulted in a 10-fold increase in Bla activity as compared to mcrBp (pBlaN). This may be explained by the fact that this mutant lacks the two neighboring CG base pairs in the centre of P1 present in all other constructs resulting in destabilization of the closing stem ([DELTA]G of P1 = -4.4 kcal/mol, Table 2). Despite the high Bla activity in the absence of the ligand, presence of tc significantly decreased Bla activity to a level compared to the other constructs resulting in a more than 11-fold regulation of gene expression.
Based on tc-RS4, two further constructs were designed. In tc-RS4a and tc-RS4b, the closing stem was elongated by one additional base pair (tc-RS4a: GC, tc-RS4b: AU). However, the additional base pair is accompanied by a decrease in Bla activity irrespective of its stability (21[+ or -]2 and 14 [+ or -] 2 mU [mg.sup.-1] for tc-RS4a and tc-RS4b, resp.). Regulation in response to tc was 2.6- and 2.0-fold, respectively, which is in the range of the constructs tc-RS1-tc-RS3. Further stabilization by increasing the length of the stem to nine base pairs resulted in even further reduction of Bla synthesis and complete loss of tc-dependent regulation (data not shown).
Of all tc-RS variants fused to mcr[B.sub.P] and investigated here six resulted in tc-dependent expression of bla. Furthermore, Bla activity in the absence of tc and the dynamic range of tc-dependent regulation varied in the constructs with respect to all parameters tested (stem length and stability, location of the RBS with respect to the stem, Table 2). The data suggest that a lower stability of the closing stem (no neighboring GC base pairs) and the partial inclusion of the RBS into the stem is beneficial for both Bla activity and regulation. Of the variants tested here tc-RS4 apparently has the optimal characteristics leading to a level of regulation (almost 12fold), which is well within the range of naturally occurring riboswitches controlling mRNA translation.
3.4. The tc-Responsive Riboswitch Is Ligand-Specific and Dose-Dependent In Vivo. As in vivo regulation of the tc-RS4 variant was highest its ligand specificity and dynamics of regulation were assessed further. The tc-RS is highly specific for tc and the lack of a hydroxyl group at position [R.sub.6][beta], resulting in dox, reduces aptamer binding by more than two orders of magnitude (0.8 nM for tc and 118 nM for dox) . To address the specificity, cells harboring the tc-RS4 construct were grown in the absence or presence of 200 [micro]M dox before Bla activity was assessed. While presence of tc in the medium leads to a ca. 12-fold reduction in Bla activity, dox had no effect on Bla activity; in the absence of antibiotic 340 [+ or -]11 mU[mg.sup.-1], and in the presence of dox 383 [+ or -] 33 mU mg-1 were determined. This observation is in full accordance with the respective dissociation constants of tc-RS determined in vitro. At the concentration used (200 [micro]M dox), formation of the ligand-stabilized aptamer does not occur due to this lower affinity and thus bla translation is not repressed. It is very unlikely that the effect observed is due to a less efficient uptake of dox by M. acetivorans because this compound efficiently mediates in vivo derepression of the artificial mcr[B.sub.P](tetO)/TetR system in this organism .
To investigate the dynamics of riboswitch regulation, cells harboring the tc-RS4 fusion were grown in the presence of increasing amounts of tc before Bla activity was determined (Figure 4). A significant reduction in Bla activity could be observed already at 7 [micro]M tc. Half-maximal reduction of bla translation was observed at ca. 14 [micro]M tc and between 50 [micro]M and 100 [micro]M tc, maximal repression of translation was achieved (Figure 4). These data are in accordance with the concentration required for complete repression in yeast . Interestingly, it is also in the same range as the tc concentration required to fully derepress the artificial mcr[B.sub.P](tetO)/TetR system in vivo (ca. 70 [micro]M) .
This work illustrates that [beta]-lactamase together with nitrocefin can be employed in Methanosarcina as a chromogenic reporter under strictly anaerobic conditions. The bla gene may be fused to any promoter allowing convenient monitoring of its expression. A secreted reporter may further aid screening purposes, like identification of trans-active mutations, on solid media. Further, establishing the solely cis-active tc-responsive riboswitch in Methanosarcina now allows conditional control of gene expression without the need of an additional factor and represents the first synthetic riboswitch described in Archaea.
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
The authors thank William W. Metcalf (Urbana, USA) for plasmid pAMG48. This work was supported by Grants from the Deutsche Forschungsgemeinschaft to B.S. and M.R. (via SFB 579, SFB902, and SU402/4-1).
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Shemsi Demolli, (1,2) Miriam M. Geist, (3,4) Julia E. Weigand, (1,5) Nicole Matschiavelli, (6) Beatrix Suess, (1,5) and Michael Rother (3,6)
(1) AG RNA Biochemie, Institutfiir Molekulare Biowissenschaften, Johann Wolfgang Goethe-Universitat Frankfurt, 60438 Frankfurt am Main, Germany
(2) Institut fur Kardiovaskulare Regeneration, Universitatsklinikum Frankfurt, Theodor-Stern-Kai 7, 60590 Frankfurt am Main, Germany
(3) AG Molekulare Mikrobiologie und Bioenergetik, Institut fur Molekulare Biowissenschaften, Johann Wolfgang Goethe-Universitat Frankfurt, 60438 Frankfurt am Main, Germany
(4) Department fur Infektiologie, Universitatsklinikum Heidelberg, Im Neuenheimer Feld 324, 69120 Heidelberg, Germany
(5) Synthetische Biologie, Fachbereich Biologie, Technische Universitat Darmstadt, 64287 Darmstadt, Germany
(6) Institut fur Mikrobiologie, Technische Universitat Dresden, 01062 Dresden, Germany
Correspondence should be addressed to Michael Rother; email@example.com
Received 27 September 2013; Accepted 2 December 2013; Published 20 January 2014
Academic Editor: William B. Whitman
Table 1: Plasmids and strains used in this study. Plasmid Construction (a)/description/relevant genotype pBR322 Source of bla gene pET28a(+) Source of [kan.sup.R] marker pAMG46 For integration into M. acetivorans hpt locus; it contains [mtaCl.sub.p] pAMG48 For integration into M. acetivorans hpt locus; it contains [mcrB.sub.p] pWM321 E. coli/M. acetivorans shuttle vector pMR56 1,176 kb AlwNI/XmnI [kan.sup.R] fragment from pET28a(+) blunted with Klenow, ligated into AhdI/ApaFI restricted and then blunted pAMG48 pBlaN 806 bp Ndel/Notl restricted blaN PCR fragment (primers 1 and 3) ligated into Ndel/Notl restricted pMR56; bla without signal peptide encoding sequence (blaN) pBlaNFSP 845 bp Ndel/Notl restricted blaNFSP PCR fragment (primers 2 and 3) ligated into Ndel/Notl restricted pMR56; bla signal peptide encoding sequence of MA3061 pMG3 1,007 bp [mtaCl.sub.p] Ndel/Bglll fragment from pAMG46 ligated into Ndel/Bglll pBlaNFSP p0145NFSP 1,424 bp Ndel/Bglll restricted [mtmCl.sub.p] PCR fragment (primers 4 and 5) ligated into Ndel/Bglll restricted, pBlaNFSP pSP64-tc-minimer Source of tc-RS encoding sequence pBlaN-prom [mcrB.sub.p] in pBlaN deleted; used as negative control pBlaN_tcRSl PCR fragment encoding tc-RSl in the [mcrB.sub.p] 5'UTR ligated into Blgll/Ndel restricted pBlaN pBlaN_tcRS2 PCR fragment encoding tc-RS2 in the [mcrB.sub.p] 5'UTR ligated into Blgll/Ndel restricted pBlaN pBlaN_tcRS3 PCR fragment encoding tc-RS3 in the [mcrB.sub.p] 5'UTR ligated into Blgll/Ndel restricted pBlaN pBlaN_tcRS4 PCR fragment encoding tc-RS4 in the [mcrB.sub.p] 5'UTR ligated into Blgll/Ndel restricted pBlaN pBlaN_tcRS4a PCR fragment encoding tc-RS4a in the [mcrB.sub.p] 5'UTR ligated into Blgll/Ndel restricted pBlaN pBlaN_tcRS4b PCR fragment encoding tc-RS2 in the [mcrB.sub.p] 5'UTR ligated into Blgll/Ndel restricted pBlaN pBlaN_tcRS5 PCR fragment encoding tc-RS5 in the [mcrB.sub.p] 5'UTR ligated into Blgll/Ndel restricted pBlaN Plasmid Reference/source pBR322  pET28a(+) Novagen pAMG46  pAMG48 Guss and Metcalf, unpublished pWM321  pMR56 This study pBlaN This study pBlaNFSP This study pMG3 This study p0145NFSP This study pSP64-tc-minimer  pBlaN-prom This study pBlaN_tcRSl This study pBlaN_tcRS2 This study pBlaN_tcRS3 This study pBlaN_tcRS4 This study pBlaN_tcRS4a This study pBlaN_tcRS4b This study pBlaN_tcRS5 This study (a) DNA sequences and maps of all plasmids are available upon request; primers used are listed in Supplementary Table SI. Table 2: tc-dependent Bla activity in M. acetivorans strains carrying [mcrB.sub.p]-tc-RS-blaN gene fusions. Bla activity (a) tc-RS -fold construct -tc +tc regulation (b) [mcrB.sub.p] 36 [+ or -] 6 39 [+ or -] 4 -- tc-RS1 104 [+ or -] 2 40 [+ or -] 2 2.6 tc-RS2 71 [+ or -] 2 40 [+ or -] 3 1.8 tc-RS3 43 [+ or -] 5 16 [+ or -] 2 2.7 tc-RS4 340 [+ or -] 10 29 [+ or -] 9 11.6 tc-RS4a 21 [+ or -] 2 8 [+ or -] 1 2.6 tc-RS4b 14 [+ or -] 2 7 [+ or -] 1 2.0 tc-RS5 1.5 [+ or -] 0.4 n.d. - P1 stability tc-RS P1 length RBS bases [DELTA]G (kcal construct (bp) in P1 [mol.sup.-1])c [mcrB.sub.p] -- -- -- tc-RS1 7 1 -5.6 tc-RS2 7 2 -5.6 tc-RS3 7 3 -5.1 tc-RS4 7 4 -4.4 tc-RS4a 8 4 -7.7 tc-RS4b 8 4 -7.7 tc-RS5 7 6 -7.1 (a) Values are given in mU (nmol [min.sup.-1]) [mg.sup.-1] and are averages of three independent cultures grown in the absence (-) or presence (+) of 200 tc; [+ or -] denotes the standard deviation; all experiments were reproduced at least once. (b) Values (-tc/+tc) were corrected by substracting those of the negative control (-prom). n.d.: below detection limit of the assay. (c) Stability was calculated using mfold (http://mfold.rna.albany.edu/).
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|Title Annotation:||Research Article|
|Author:||Demolli, Shemsi; Geis, Miriam M.; Weigand, Julia E.; Matschiavelli, Nicole; Suess, Beatrix; Rother,|
|Date:||Jan 1, 2014|
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