Novel Aspects of Polynucleotide Phosphorylase Function in Streptomyces

Polynucleotide phosphorylase (PNPase) is a 3′–5′-exoribnuclease that is found in most bacteria and in some eukaryotic organelles. The enzyme plays a key role in RNA decay in these systems. PNPase structure and function have been studied extensively in Escherichia coli, but there are several important aspects of PNPase function in Streptomyces that differ from what is observed in E. coli and other bacterial genera. This review highlights several of those differences: (1) the organization and expression of the PNPase gene in Streptomyces; (2) the possible function of PNPase as an RNA 3′-polyribonucleotide polymerase in Streptomyces; (3) the function of PNPase as both an exoribonuclease and as an RNA 3′-polyribonucleotide polymerase in Streptomyces; (4) the function of (p)ppGpp as a PNPase effector in Streptomyces. The review concludes with a consideration of a number of unanswered questions regarding the function of Streptomyces PNPase, which can be examined experimentally.


Introduction
Polynucleotide phosphorylase (PNPase, EC 2.7.7.8) was the first enzyme shown to synthesize polyribonucleotides [1], and for some time, it was thought to be the bacterial RNA polymerase. The enzyme was subsequently characterized in Escherichia coli and other bacteria, and was shown to catalyze the following reaction: (p 5′ N 3′ OH)X + Pi  (p 5′ N 3′ OH)X−1 + pp 5′ N where N is any of the four bases found in RNA [2,3]. As written, the reaction depicts the phosphorolytic degradation of RNA chains, and this activity appears to reflect the major function of PNPase in vivo. The reaction is reversible, however, and PNPase will synthesize polyribonucleotide chains, using nucleoside diphosphates (NDPs), rather than triphosphates, as substrates. The polymerizing activity of PNPase played an important role in the synthesis of polyribonucleotides used to unravel the genetic code [4,5].
PNPase is found in all bacteria examined to date, except Mycoplasma, and is also present in eukaryotic organelles [6]. The enzyme has not been identified in Archaea [7]. In E. coli, PNPase and RNase II are the major 3′-exonucleases involved in RNA degradation [8]. In addition to its degradative function, PNPase plays a role in the bacterial response to environmental stresses, such as cold shock [9][10][11], is involved in biofilm formation [12,13] and virulence determination [14,15], and the activity of the enzyme is modulated by a number of small molecule effectors, at least in vitro [16][17][18][19].
Streptomyces are Gram-positive, soil-dwelling bacteria, notable for their ability to form spores and for their capacity to produce antibiotics [20,21]. Nearly 70% of all antibiotics used in clinical and (p 5 N 3 OH) X−1 + pp 5 N where N is any of the four bases found in RNA [2,3]. As written, the reaction depicts the phosphorolytic degradation of RNA chains, and this activity appears to reflect the major function of PNPase in vivo. The reaction is reversible, however, and PNPase will synthesize polyribonucleotide chains, using nucleoside diphosphates (NDPs), rather than triphosphates, as substrates. The polymerizing activity of PNPase played an important role in the synthesis of polyribonucleotides used to unravel the genetic code [4,5].
PNPase is found in all bacteria examined to date, except Mycoplasma, and is also present in eukaryotic organelles [6]. The enzyme has not been identified in Archaea [7]. In E. coli, PNPase and RNase II are the major 3 -exonucleases involved in RNA degradation [8]. In addition to its degradative function, PNPase plays a role in the bacterial response to environmental stresses, such as cold shock [9][10][11], is involved in biofilm formation [12,13] and virulence determination [14,15], and the activity of the enzyme is modulated by a number of small molecule effectors, at least in vitro [16][17][18][19].
Streptomyces are Gram-positive, soil-dwelling bacteria, notable for their ability to form spores and for their capacity to produce antibiotics [20,21]. Nearly 70% of all antibiotics used in clinical and veterinary medicine worldwide are synthesized as natural products by members of the genus [22]. Of particular relevance to this review, a number of biochemical and genetic features of Streptomyces PNPase distinguish it from its counterparts in other bacteria. In what follows, the functions of PNPase in Streptomyces will be explored. The reader is referred to several excellent reviews as sources of additional information on PNPase from E. coli and other bacteria [2,3,23,24].

Organization and Expression of the PNPase Gene in Streptomyces
In E. coli, and other organisms that have been studied, the PNPase gene, pnp, is a part of an operon that also includes rpsO, the gene for ribosomal protein S15 [9,25,26]. That operon is transcribed from two promoters in E. coli, designated PrpsO and Ppnp [25,27]. PrpsO is situated upstream of the rpsO gene, and Ppnp is located in the intergenic region between the two genes. Transcription from PrpsO ends at a rho-independent terminator and produces the rpsO transcript, but transcription through this terminator occurs with significant frequency and produces a readthrough transcript, containing both rpsO and pnp. Transcription from the intergenic promoter, Ppnp, produces a transcript containing pnp only [25,27]. In addition to the rpsO terminator, the rpsO-pnp intergenic region contains a second stem-loop that functions as a processing site for the double strand specific endoribonuclease, RNase III. RNase III processing plays an important role in pnp expression [25,[28][29][30].
Our interest in the mechanisms of RNA decay in Streptomyces led to an examination of the transcriptional organization of the rpsO-pnp operon in Streptomyces coelicolor, the paradigm for biological studies in the genus. To our surprise, primer extension analysis of RNAs isolated from a parental strain of S. coelicolor and from an RNase III null mutant revealed not two, but four extension products, suggesting the presence of four promoters within the rpsO-pnp operon [31]. A visual inspection of 162 putative Streptomyces promoters from Strohl [32] and Yamazaki et al. [33], and a group of synthetic promoters generated by Seghezzi et al. [34], indicated that all four of the 5 -ends identified by primer extension in our studies were preceded by sequences similar to the −10 and −35 regions of characterized streptomycete promoters. Promoter probe cloning of DNA fragments containing these putative promoter sequences verified that the rpsO-pnp operon of S. coelicolor is transcribed from four promoters, two situated upstream of rpsO (PrpsOA and PrpsOB) and two situated in the intergenic region, upstream of pnp (PpnpA and PpnpB, Figure 1). veterinary medicine worldwide are synthesized as natural products by members of the genus [22]. Of particular relevance to this review, a number of biochemical and genetic features of Streptomyces PNPase distinguish it from its counterparts in other bacteria. In what follows, the functions of PNPase in Streptomyces will be explored. The reader is referred to several excellent reviews as sources of additional information on PNPase from E. coli and other bacteria [2,3,23,24].

Organization and Expression of the PNPase Gene in Streptomyces
In E. coli, and other organisms that have been studied, the PNPase gene, pnp, is a part of an operon that also includes rpsO, the gene for ribosomal protein S15 [9,25,26]. That operon is transcribed from two promoters in E. coli, designated PrpsO and Ppnp [25,27]. PrpsO is situated upstream of the rpsO gene, and Ppnp is located in the intergenic region between the two genes. Transcription from PrpsO ends at a rho-independent terminator and produces the rpsO transcript, but transcription through this terminator occurs with significant frequency and produces a readthrough transcript, containing both rpsO and pnp. Transcription from the intergenic promoter, Ppnp, produces a transcript containing pnp only [25,27]. In addition to the rpsO terminator, the rpsOpnp intergenic region contains a second stem-loop that functions as a processing site for the double strand specific endoribonuclease, RNase III. RNase III processing plays an important role in pnp expression [25,[28][29][30].
Our interest in the mechanisms of RNA decay in Streptomyces led to an examination of the transcriptional organization of the rpsO-pnp operon in Streptomyces coelicolor, the paradigm for biological studies in the genus. To our surprise, primer extension analysis of RNAs isolated from a parental strain of S. coelicolor and from an RNase III null mutant revealed not two, but four extension products, suggesting the presence of four promoters within the rpsO-pnp operon [31]. A visual inspection of 162 putative Streptomyces promoters from Strohl [32] and Yamazaki et al. [33], and a group of synthetic promoters generated by Seghezzi et al. [34], indicated that all four of the 5′-ends identified by primer extension in our studies were preceded by sequences similar to the −10 and −35 regions of characterized streptomycete promoters. Promoter probe cloning of DNA fragments containing these putative promoter sequences verified that the rpsO-pnp operon of S. coelicolor is transcribed from four promoters, two situated upstream of rpsO (PrpsOA and PrpsOB) and two situated in the intergenic region, upstream of pnp (PpnpA and PpnpB, Figure 1 PpnpA, B represent the upstream and intergenic promoters found in S. coelicolor, respectively. The ball-and-stick structures immediately following rpsO and pnp represent rho-independent transcription terminators. The ball-and-stick structure just upstream of pnp represents the intergenic hairpin which is cleaved by RNase III. The diagram is not drawn to scale.
Of particular interest in this analysis was the observation that the four promoters were temporally regulated. That is, the activity of the four promoters varied with time after inoculation of liquid cultures and the variations were promoter-specific, as shown in Figure 2. In terms of maximal activity, PpnpB was most active followed by PrpsOB, PpnpA, and PrpsOA. PpnpA, B represent the upstream and intergenic promoters found in S. coelicolor, respectively. The ball-and-stick structures immediately following rpsO and pnp represent rho-independent transcription terminators. The ball-and-stick structure just upstream of pnp represents the intergenic hairpin which is cleaved by RNase III. The diagram is not drawn to scale.
Of particular interest in this analysis was the observation that the four promoters were temporally regulated. That is, the activity of the four promoters varied with time after inoculation of liquid cultures and the variations were promoter-specific, as shown in Figure 2. In terms of maximal activity, PpnpB was most active followed by PrpsOB, PpnpA, and PrpsOA. coelicolor derivatives containing the putative rpsOA and rpsOB promoters, cloned in the promoter probe vector pIPP2 [35]. Mycelium was harvested at the indicated times, disrupted by sonication, and following centrifugation, supernatants were assayed for catechol dioxygenase, as described previously [31,35]. The catechol dioxygenase gene is the reporter in the promoter probe vector [35]. A major mechanism for the modulation of promoter activity in bacterial systems involves the use of alternative sigma factors by RNA polymerase. The S. coelicolor genome encodes over sixty alternative sigma factors, many of which play roles in differentiation and responses to stress (reviewed in [36]). It was of considerable interest to determine whether the four rpsO-pnp promoters might require alternative sigma factors for transcription in S. coelicolor.
To this end, we obtained null mutants for a number of sigma factors, including σ B , σ H , and σ L [36], and their corresponding parental strains. We transferred the rpsO-pnp promoter probe constructs to each strain and measured promoter activity. The results obtained for the σ H and σ L mutants were quite similar to those for the parental strain of S. coelicolor, that is, the same pattern of temporal regulation was observed in both of these sigma factor mutants as in the parental strain (cf. Figure 2). In marked contrast, the PrpsOA, PrpsOB, and PpnpB promoters were completely inactive in the σ B mutant. PpnpA, however, was as active in the σ B mutant as in the parental strain, and showed a similar pattern of temporal expression [31]. This result indicates that PrpsOA and B and PpnpB are dependent on σ B for activity, and suggests that these promoters are transcribed by an RNA polymerase holoenzyme containing σ B .
PNPase is a cold shock protein in many bacteria, and it has been shown that cold shock leads to an increase in PNPase levels in E. coli and other organisms [9][10][11]. It was of interest to determine whether PNPase levels increased in cold shock in S. coelicolor, and whether any such increase  [35]. Mycelium was harvested at the indicated times, disrupted by sonication, and following centrifugation, supernatants were assayed for catechol dioxygenase, as described previously [31,35]. The catechol dioxygenase gene is the reporter in the promoter probe vector [35]. A major mechanism for the modulation of promoter activity in bacterial systems involves the use of alternative sigma factors by RNA polymerase. The S. coelicolor genome encodes over sixty alternative sigma factors, many of which play roles in differentiation and responses to stress (reviewed in [36]). It was of considerable interest to determine whether the four rpsO-pnp promoters might require alternative sigma factors for transcription in S. coelicolor.
To this end, we obtained null mutants for a number of sigma factors, including σ B , σ H , and σ L [36], and their corresponding parental strains. We transferred the rpsO-pnp promoter probe constructs to each strain and measured promoter activity. The results obtained for the σ H and σ L mutants were quite similar to those for the parental strain of S. coelicolor, that is, the same pattern of temporal regulation was observed in both of these sigma factor mutants as in the parental strain (cf. Figure 2). In marked contrast, the PrpsOA, PrpsOB, and PpnpB promoters were completely inactive in the σ B mutant. PpnpA, however, was as active in the σ B mutant as in the parental strain, and showed a similar pattern of temporal expression [31]. This result indicates that PrpsOA and B and PpnpB are dependent on σ B for activity, and suggests that these promoters are transcribed by an RNA polymerase holoenzyme containing σ B .
PNPase is a cold shock protein in many bacteria, and it has been shown that cold shock leads to an increase in PNPase levels in E. coli and other organisms [9][10][11]. It was of interest to determine whether PNPase levels increased in cold shock in S. coelicolor, and whether any such increase reflected changes in the activity of the rpsO-pnp promoters. As shown in Figure 3C, PNPase activity increased significantly (two-fold) in S. coelicolor over three hours of cold shock at 10 • C. This increase in activity was accompanied by an increase in the activities of all four of the rpsO-pnp promoters ( Figure 3A,B) as compared with their activities at the normal growth temperature, 30 • C.
Antibiotics 2018, 7, x 4 of 13 reflected changes in the activity of the rpsO-pnp promoters. As shown in Figure 3C, PNPase activity increased significantly (two-fold) in S. coelicolor over three hours of cold shock at 10 °C. This increase in activity was accompanied by an increase in the activities of all four of the rpsO-pnp promoters (Figure 3 A,B) as compared with their activities at the normal growth temperature, 30 °C. Figure 3. Cold shock responses of S. coelicolor. Derivatives containing the rpsO-pnp promoter probe constructs were grown and 30 °C , and half of each culture was then shifted to 10 °C. Mycelium was harvested at the indicated times, disrupted by sonication, and following centrifugation, supernatants were assayed for promoter activity, as described [31,35]. Panel C shows the results of PNPase polymerization assays. In Panels A and B, PNPase promoter activities are expressed relative to the activity measured at 30 °C at zero time, immediately before the shift to 10 °C. The results shown are the averages of duplicate assays from two independent experiments ± SEM. In the first experiment, Thus, PNPase is a cold shock protein in Streptomyces, and the cold shock response involves changes in the activities of the promoters responsible for transcription of the rpsO-pnp operon [31].

PNPase Function as an RNA 3′-Polyribonucleotide Polymerase in Streptomyces
As is the case in eukaryotes, bacterial RNAs have oligo-and polyribonucleotide tails at their 3′-ends, and these tails are added post-transcriptionally (reviewed in [37]). In E. coli, the primary enzyme responsible for the synthesis of these tails is poly(A) polymerase I (PAP I), and the tails are composed primarily of A residues [38]. In bacteria, poly(A) tails function to facilitate RNA degradation as the major 3′-exoribonucleases, viz. RNase II and PNPase in E. coli, digest these tails processively in vitro and in vivo [8,39].
It was shown some years ago by Mohanty and Kushner that an E. coli mutant lacking PAP I still added tails to the 3′-ends of its RNAs. However, these tails were not composed exclusively of A Figure 3. Cold shock responses of S. coelicolor. Derivatives containing the rpsO-pnp promoter probe constructs were grown and 30 • C, and half of each culture was then shifted to 10 • C. Mycelium was harvested at the indicated times, disrupted by sonication, and following centrifugation, supernatants were assayed for promoter activity, as described [31,35]. Panel C shows the results of PNPase polymerization assays. In Panels A and B, PNPase promoter activities are expressed relative to the activity measured at 30 • C at zero time, immediately before the shift to 10 • C. The results shown are the averages of duplicate assays from two independent experiments ± SEM. In the first experiment, PNPase levels were measured in S. coelicolor containing PrpsOA and in the second, PNPase levels were Thus, PNPase is a cold shock protein in Streptomyces, and the cold shock response involves changes in the activities of the promoters responsible for transcription of the rpsO-pnp operon [31].

PNPase Function as an RNA 3 -Polyribonucleotide Polymerase in Streptomyces
As is the case in eukaryotes, bacterial RNAs have oligo-and polyribonucleotide tails at their 3 -ends, and these tails are added post-transcriptionally (reviewed in [37]). In E. coli, the primary enzyme responsible for the synthesis of these tails is poly(A) polymerase I (PAP I), and the tails are composed primarily of A residues [38]. In bacteria, poly(A) tails function to facilitate RNA degradation as the major 3 -exoribonucleases, viz. RNase II and PNPase in E. coli, digest these tails processively in vitro and in vivo [8,39].
It was shown some years ago by Mohanty and Kushner that an E. coli mutant lacking PAP I still added tails to the 3 -ends of its RNAs. However, these tails were not composed exclusively of A residues; the tails contained G, C, and U residues as well, i.e., they were heteropolymeric [40]. Mohanty and Kushner demonstrated that the enzyme responsible for the synthesis of these heteropolymeric tails was none other than PNPase [40]. Thus, even in the absence of PAP I, PNPase can add 3 -tails to facilitate the degradation of cellular RNAs.
Streptomyces do not contain PAP I. Yet the 3 -ends of streptomycete RNAs do possess tails. Moreover, the tails are heteropolymeric in composition, like those synthesized by PNPase in E. coli in the absence of PAP I [41,42]. These observations, and the report that PNPase functions as the RNA 3 -polyribonucleotide polymerase in plant chloroplasts and in cyanobacteria [43,44], led to the hypothesis that PNPase played the same role in Streptomyces [45]. The straightforward way to test this hypothesis would be to create a pnp null mutant, e.g., in S. coelicolor, and to determine whether the mutant was still capable of adding 3 -tails to its RNAs. However, attempts to disrupt pnp in S. coelicolor and in the sister species, Streptomyces antibioticus, were only successful when a second copy of pnp was added to the genome. In other words, gene disruption attempts revealed that, unlike the situation in E. coli and in the Bacilli, pnp is an essential gene in Streptomyces [42].
A model for the function of PNPase as an RNA 3 -polyribonucleotide polymerase is presented in detail below.

Function of PNPase as Both an Exoribonuclease and as an RNA 3 -Polyribonucleotide Polymerase
PNPase activity is highly processive and the enzyme is impeded by stem-loop structures [46]. Streptomycete genomes are GC rich, so that enzymes involved in RNA decay may have evolved to degrade the RNAs derived from these genomes efficiently. A possible strategy for facilitating this degradation was suggested by the observation that PNPase appears to utilize its polymerizing activity to add 3 -tails to streptomycete RNAs [42,45]. It seemed possible that the enzyme might add such tails during phosphorolysis to create single stranded 3 -ends that would then function as the substrates for that phosphorolysis. If this were the case, it might be expected that nucleoside diphosphates, the substrates for polymerization, would stimulate phosphorolysis. To test this hypothesis, two model PNPase substrates were constructed from the sequence of the rpsO-pnp operon of S. coelicolor. Both substrates contained the rpsO-pnp terminator and the intergenic hairpin. Thus, both model substrates contained secondary structure that would be expected to impede phosphorolysis by PNPase. One substrate, designated 5601, also possessed a single stranded 3 -tail, 33 bases in length, while the other substrate, 5650, terminated at the base of the intergenic hairpin, and did not have a single stranded tail [47].
The phosphorolysis of these two substrates was studied in the absence and presence of a mixture of all four nucleoside diphosphates (NDPs) with the interesting result, predicted by our hypothesis, that the NDPs, normally the substrates for the polymerizing activity of PNPase, did stimulate RNA degradation by phosphorolysis. Figure 4 shows the results of phosphorolysis of the 5650 transcript (labeled RP3 in the figure).
Analysis of the results shown in Figure 4 revealed that NDPs at 20-30 µM in phosphorolysis mixtures stimulated that reaction by 2-3 fold as compared with controls, but only when the structured RNA, 5650 (RP3) was used as the substrate [47]. NDPs had no effect on the phosphorolysis of the 5601 substrate, possessing the single stranded tail. Kinetic analyses showed that NDPs affected the K m for phosphorolysis. Thus, the K m value for phosphorolysis of the 5650 substrate in the absence of NDPs was 3.1 µM. This value decreased to 0.65 µM in the presence of all four NDPs at 20 µM. This latter K m was almost identical to that obtained in the absence of NDPs for the 5601 substrate, which has a single stranded 3 -tail (0.62 µM). NDPs did not further decrease the K m for the 5601 substrate. It is noteworthy as well, that NDPs had no effect on the phosphorolysis of either substrate by E. coli PNPase, and that the E. coli enzyme was intrinsically less active with the structured substrate than was its counterpart from S. coelicolor [47]. Phosphorolysis reactions were performed as described in [47], and reaction products were separated by gel electrophoresis. The top panel shows the results obtained with S. coelicolor PNPase and the bottom panel results using E. coli PNPase. Reactions were conducted in the presence of increasing concentrations of a mixture of ADP, CDP, UDP, and GDP (nucleoside diphosphates (NDPs)) as indicated. RP3 is the 5650 transcript, and RP4 represents the product obtained by complete digestion of the intergenic hairpin in RP3 by PNPase. Note that as PNPase is highly processive [48], no intermediates with mobilities between those of RP3 and RP4 were observed. Copyright © American Society for Microbiology (J. Bacteriol. 190, 2008, 98-106, DOI:10.1128/JB.00327-07) [47].
Analysis of the results shown in Figure 4 revealed that NDPs at 20-30 µ M in phosphorolysis mixtures stimulated that reaction by 2-3 fold as compared with controls, but only when the structured RNA, 5650 (RP3) was used as the substrate [47]. NDPs had no effect on the phosphorolysis of the 5601 substrate, possessing the single stranded tail. Kinetic analyses showed that NDPs affected the Km for phosphorolysis. Thus, the Km value for phosphorolysis of the 5650 substrate in the absence of NDPs was 3.1 µ M. This value decreased to 0.65 µ M in the presence of all four NDPs at 20 µ M. This latter Km was almost identical to that obtained in the absence of NDPs for the 5601 substrate, which has a single stranded 3′-tail (0.62 µ M). NDPs did not further decrease the Km for the 5601 substrate. It is noteworthy as well, that NDPs had no effect on the phosphorolysis of either substrate by E. coli PNPase, and that the E. coli enzyme was intrinsically less active with the structured substrate than was its counterpart from S. coelicolor [47].
Our model for the explanation of the foregoing observations is shown in Figure 5 [49]. Phosphorolysis reactions were performed as described in [47], and reaction products were separated by gel electrophoresis. The top panel shows the results obtained with S. coelicolor PNPase and the bottom panel results using E. coli PNPase. Reactions were conducted in the presence of increasing concentrations of a mixture of ADP, CDP, UDP, and GDP (nucleoside diphosphates (NDPs)) as indicated. RP3 is the 5650 transcript, and RP4 represents the product obtained by complete digestion of the intergenic hairpin in RP3 by PNPase. Note that as PNPase is highly processive [48], no intermediates with mobilities between those of RP3 and RP4 were observed. Copyright © American Society for Microbiology (J. Bacteriol. 190, 2008, 98-106, DOI:10.1128/JB.00327-07) [47].
Our model for the explanation of the foregoing observations is shown in Figure 5 [49]. We posit that the stem-loops of structured substrates, like 5650, block PNPase action. The addition of short 3 -tails during phosphorolysis, or the presence of naturally occurring tails on substrates like 5601, allows for the breathing of stems and thus permits PNPase, which might otherwise stall at the stem-loops in structured substrates, to continue phosphorolysis through those structures. As indicated above, this mechanism may represent an evolutionary adaptation occasioned by the high GC content of streptomycete genomes and their transcripts.
It must be noted, however, that the evidence for the function of PNPase as a 3 -polyribonucleotide polymerase in Streptomyces is indirect. In vivo evidence for this function remains to be uncovered. We posit that the stem-loops of structured substrates, like 5650, block PNPase action. The addition of short 3′-tails during phosphorolysis, or the presence of naturally occurring tails on substrates like 5601, allows for the breathing of stems and thus permits PNPase, which might otherwise stall at the stem-loops in structured substrates, to continue phosphorolysis through those structures. As indicated above, this mechanism may represent an evolutionary adaptation occasioned by the high GC content of streptomycete genomes and their transcripts.
It must be noted, however, that the evidence for the function of PNPase as a 3′-polyribonucleotide polymerase in Streptomyces is indirect. In vivo evidence for this function remains to be uncovered.
PNPase from S. antibioticus was shown to synthesize pppGpp in vitro [57,58]. While this activity may be an in vitro artifact, as no other PNPases are known to possess it, the observation suggested a possible relationship between (p)ppGpp and RNA decay in Streptomyces. To begin to examine this relationship, the effects of (p)ppGpp on polymerization and phosphorolysis by S. coelicolor, S. antibioticus, and E. coli PNPases were measured in the absence and presence of (p)ppGpp [59]. As
PNPase from S. antibioticus was shown to synthesize pppGpp in vitro [57,58]. While this activity may be an in vitro artifact, as no other PNPases are known to possess it, the observation suggested a possible relationship between (p)ppGpp and RNA decay in Streptomyces. To begin to examine this relationship, the effects of (p)ppGpp on polymerization and phosphorolysis by S. coelicolor, S. antibioticus, and E. coli PNPases were measured in the absence and presence of (p)ppGpp [59]. As shown in Figure 6, both guanosine penta-and tetraphosphates inhibited the activity of S. coelicolor PNPase, in both phosphorolysis and polymerization, though ppGpp was a more potent inhibitor than pppGpp.
Essentially identical results were obtained for S. antibioticus PNPase (not shown). By contrast, neither ppGpp nor pppGpp were effective inhibitors of the activity of E. coli PNPase. Indeed, at concentrations up to 1 mM, pppGpp actually stimulated the polymerizing activity of the E. coli enzyme.
shown in Figure 6, both guanosine penta-and tetraphosphates inhibited the activity of S. coelicolor PNPase, in both phosphorolysis and polymerization, though ppGpp was a more potent inhibitor than pppGpp. Figure 6. Effects of (p)ppGpp on the activity of PNPase. Polymerization and phosphorolysis reactions were performed in the absence and presence of guanosine tetraphosphate (ppGpp) or guanosine pentaphosphate (pppGpp), using purified PNPase from S. coelicolor and E. coli [59]. Results are expressed relative to the activities measured in the absence of (p)ppGpp, set arbitrarily to 100%.
Essentially identical results were obtained for S. antibioticus PNPase (not shown). By contrast, neither ppGpp nor pppGpp were effective inhibitors of the activity of E. coli PNPase. Indeed, at concentrations up to 1 mM, pppGpp actually stimulated the polymerizing activity of the E. coli enzyme.
In the same study, the effects of (p)ppGpp on the stability of bulk mRNA in S. coelicolor were examined [59]. It was initially observed that the half-life of bulk mRNA increased by 1.8-fold in stationary phase cultures as compared with exponential phase. That this increase might be related to the effects of (p)ppGpp was suggested by studies with an S. coelicolor relA mutant, and a strain containing an inducible relA gene. While the half-life of bulk mRNA was longer in the relA mutant than in the parental strain (e.g., 8.9 min vs 3.2 min in exponential phase), the half-life decreased slightly in the relA mutant in stationary phase (to 7.2 min). In the strain containing an inducible relA gene, producing increased levels of (p)ppGpp, induction occasioned a ca. two-fold increase in the half-life of bulk mRNA, from 6.6 to 11.8 min. Taken together, these observations suggest that (p)ppGpp may stabilize mRNAs in stationary phase S. coelicolor cells, as compared with cells growing exponentially.
Why and how might this stabilization occur? It is well established that although levels of RNA and protein synthesis decrease dramatically as Streptomyces cultures move from the exponential to the stationary phase of growth, a basal level of synthesis is maintained throughout stationary phase [60,61]. This basal level of macromolecular synthesis is presumably required to produce enzymes and other proteins involved in the synthesis of the secondary metabolites these organisms produce in stationary phase. Stabilization of the transcripts for these proteins would represent one strategy the organisms could employ to ensure the persistence of macromolecular synthesis to support secondary metabolite production. It is known that (p)ppGpp is present in significant amounts, even in stationary phase streptomycete cultures [62,63]. Thus, the inhibition of PNPase by (p)ppGpp Figure 6. Effects of (p)ppGpp on the activity of PNPase. Polymerization and phosphorolysis reactions were performed in the absence and presence of guanosine tetraphosphate (ppGpp) or guanosine pentaphosphate (pppGpp), using purified PNPase from S. coelicolor and E. coli [59]. Results are expressed relative to the activities measured in the absence of (p)ppGpp, set arbitrarily to 100%.
In the same study, the effects of (p)ppGpp on the stability of bulk mRNA in S. coelicolor were examined [59]. It was initially observed that the half-life of bulk mRNA increased by 1.8-fold in stationary phase cultures as compared with exponential phase. That this increase might be related to the effects of (p)ppGpp was suggested by studies with an S. coelicolor relA mutant, and a strain containing an inducible relA gene. While the half-life of bulk mRNA was longer in the relA mutant than in the parental strain (e.g., 8.9 min vs 3.2 min in exponential phase), the half-life decreased slightly in the relA mutant in stationary phase (to 7.2 min). In the strain containing an inducible relA gene, producing increased levels of (p)ppGpp, induction occasioned a ca. two-fold increase in the half-life of bulk mRNA, from 6.6 to 11.8 min. Taken together, these observations suggest that (p)ppGpp may stabilize mRNAs in stationary phase S. coelicolor cells, as compared with cells growing exponentially.
Why and how might this stabilization occur? It is well established that although levels of RNA and protein synthesis decrease dramatically as Streptomyces cultures move from the exponential to the stationary phase of growth, a basal level of synthesis is maintained throughout stationary phase [60,61]. This basal level of macromolecular synthesis is presumably required to produce enzymes and other proteins involved in the synthesis of the secondary metabolites these organisms produce in stationary phase. Stabilization of the transcripts for these proteins would represent one strategy the organisms could employ to ensure the persistence of macromolecular synthesis to support secondary metabolite production. It is known that (p)ppGpp is present in significant amounts, even in stationary phase streptomycete cultures [62,63]. Thus, the inhibition of PNPase by (p)ppGpp might represent a strategy used by Streptomyces to stabilize essential mRNAs during stationary phase. It would be interesting to determine whether (p)ppGpp inhibits the activity of other exo-and endonucleases and while such analyses have yet to be performed, it is noteworthy that ppGpp inhibits PNPase from another actinomycete, Nonomuraea sp. [64].

Conclusions and Unanswered Questions
It is apparent from the brief analysis above that PNPase is a multitalented enzyme that plays a critical role in the metabolic activities of bacterial cells. Despite the wealth of information that has been accumulated about PNPase, a number of important biological questions remain unanswered, particularly as they relate to the functions of Streptomyces PNPase.
First, why is the rpsO-pnp operon of S. coelicolor transcribed from four promoters? The answer to this question may relate to the fact that the operon contains a ribosomal protein gene, as well as the gene for PNPase. It is possible that the promoters are not only critical to the regulation of pnp expression, but that they also play and important role in ribosome biogenesis via their regulation of the levels of the rpsO transcript. Mutation of the four promoter sequences may provide insight into these possibilities.
Second, what is the significance, if there is any, to the fact that the S. coelicolor rpsO-pnp operon produces six transcripts (two rpsO transcripts from PrpsOA and B, two readthrough transcripts from the same two promoters, and two pnp transcripts from PpnpA and B)? It should be noted that Northern blot analysis of the transcripts derived from the S. coelicolor rpsO-pnp operon did not reveal the presence of six separate transcripts [65]. It is possible that the different transcripts are not sufficiently different in size to have been resolved on the Northern blotting gels. Another intriguing possibility is that the longer transcripts, obtained from the upstream promoter in each case, might be processed at their 5 -ends by RNase J, which possesses 5 -3 -exoribonuclease activity. RNase J has recently been characterized in S. coelicolor [66,67].
Third, as described above, PNPase is a cold shock protein in Streptomyces. It is relevant to ask whether PNPase responds to other environmental stresses, such as heat, oxidative stress, metal ion stress, etc. It would be of interest, in particular, to examine the effects of various types of stress on the activities of the rpsO-pnp promoters. Mutational analyses again might reveal important aspects of promoter function in stress conditions in Streptomyces.
Fourth, a number of small effector molecules modulate the activity of E. coli PNPase, e.g., ATP, citrate, and cyclic-diGMP [16][17][18][19]. It has been proposed that these effectors connect RNA decay to other metabolic pathways in bacterial cells. It would be interesting to determine whether these effectors also affect the activity of Streptomyces PNPase. It is noteworthy, in this regard, that in silico molecular docking studies suggest that citrate, which inhibits the activity of E. coli PNPase, will bind to PNPase from S. antibioticus [18].
Finally, in E. coli and other organisms, PNPase is part of a larger macromolecular complex generally referred to as the degradosome ( [68,69]. In E. coli, the components of the degradosome are organized around a scaffold provided by the single strand specific endoribonuclease, RNase E [70]. RNase E is present in S. coelicolor, and has been shown to interact with PNPase in vivo [71]. However, unlike the situation in E. coli, the identities of other proteins that might be involved in the degradative machine are unknown in Streptomyces.
It is fervently hoped that the foregoing and other important questions related to PNPase structure and function will continue to attract interest and experimentation to provide answers to them.