- Open Access
Understanding of bacterial lignin extracellular degradation mechanisms by Pseudomonas putida KT2440 via secretomic analysis
Biotechnology for Biofuels and Bioproducts volume 15, Article number: 117 (2022)
Bacterial lignin degradation is believed to be primarily achieved by a secreted enzyme system. Effects of such extracellular enzyme systems on lignin structural changes and degradation pathways are still not clearly understood, which remains as a bottleneck in the bacterial lignin bioconversion process.
This study investigated lignin degradation using an isolated secretome secreted by Pseudomonas putida KT2440 that grew on glucose as the only carbon source. Enzyme assays revealed that the secretome harbored oxidase and peroxidase/Mn2+-peroxidase capacity and reached the highest activity at 120 h of the fermentation time. The degradation rate of alkali lignin was found to be only 8.1% by oxidases, but increased to 14.5% with the activation of peroxidase/Mn2+-peroxidase. Gas chromatography–mass spectrometry (GC–MS) and two-dimensional 1H–13C heteronuclear single-quantum coherence (HSQC) NMR analysis revealed that the oxidases exhibited strong C–C bond (β-β, β-5, and β-1) cleavage. The activation of peroxidases enhanced lignin degradation by stimulating C–O bond (β-O-4) cleavage, resulting in increased yields of aromatic monomers and dimers. Further mass spectrometry-based quantitative proteomics measurements comprehensively identified different groups of enzymes particularly oxidoreductases in P. putida secretome, including reductases, peroxidases, monooxygenases, dioxygenases, oxidases, and dehydrogenases, potentially contributed to the lignin degradation process.
Overall, we discovered that bacterial extracellular degradation of alkali lignin to vanillin, vanillic acid, and other lignin-derived aromatics involved a series of oxidative cleavage, catalyzed by active DyP-type peroxidase, multicopper oxidase, and other accessory enzymes. These results will guide further metabolic engineering design to improve the efficiency of lignin bioconversion.
The current vision of biorefinery undervalues lignin’s potential to address this nation’s high demands on quality liquid fuel, chemicals and biomaterials [1,2,3,4,5,6,7,8]. Lignin is an abundant natural component from plant biomass, but remains challenging in bioconversion process due to its recalcitrant polymeric structure [9, 10], while the highly heterogeneous linkages among its aromatic centers, including a variety of C–O–C bonds (β-O-4/4′, α-O-4/4′, α/γ-O-γ, 4-O-5/5′, etc.) and C–C bonds (5–5/5′, β-β, β-1, β-5, etc.) [1,2,3]. To improve the bioconversion of lignocellulosic feedstocks, more effective lignin degradation methods are in demand. Approaches published for lignin degradation and conversion include chemical degradation and enzymatic lignin breakdown [4, 11,12,13,14,15,16,17,18,19,20,21,22]. Compared to the chemical and thermal degradation, enzymatic lignin breakdown is low cost and environmentally friendly [4, 5, 23]. Nature has found ways to degrade lignin by producing dedicated ligninolytic enzyme systems [24, 25]. While such enzymes have been thoroughly studied for ligninolytic fungi [26,27,28], reports on bacterial enzymes capable of lignin modification have been relatively new in recent years [13, 27, 29, 30]. Several types of oxidoreductases that enable bacteria to act on lignin have been revealed [12, 31,32,33,34].
As a lignin-degrading bacteria, Pseudomonas putida KT2440 has catabolic potential against a wide range of natural aromatic compounds. Linger et al. demonstrated the lignin breakdown products bioconversion capacity in P. putida KT2440 . The presence of P. putida KT2440 with fungal secretome enhanced lignin degradation possible due to the catabolism of low-molecular-weight lignin and partially prevent of repolymerization . Continuous oxidative enzymes that might be involved in lignin break down processes are identified consistently in P. putida. Screening studies reported P. putida KT2440 secreted ligninolytic enzymes such as laccase, Mn2+-independent peroxidase (e.g., DyP), and Mn2+-oxidizing peroxidase (e.g., MnP and DyP) . Multicopper oxidase (CopA) from P. putida KT2440 was characterized afterward with the lignin model compounds oxidizing ability .Furthermore, β-etherase (glutathione S-transferases, GSTs) and dioxygenases (e.g., 2,3-quercetin dioxygenase) were upregulated in the secretome of P. putida when exposed to lignin. Moreover, multicopper oxidase such as CopA was also detected in the secretome when P. putida grew on lignin-free media (glucose), suggesting the possibility of other carbon sources (e.g., glucose) could also induce oxidoreductases that might be involved in lignin catabolism process. In addition, spatiotemporal mechanisms for lignin catabolism in P. putida KT2440 have revealed that outer membrane vesicle (OMVs) would encapsulate enzymes involved in the catabolism of lignin-derived aromatic structures . However, the oxidative lignin degradation enzymes in P. putida KT2440 are under-identified, which requires more efforts to explore potential enzymes.
Understanding the extracellular degradation pathways and lignin structural changes by Pseudomonas putida KT2440 is critical for developing processes for efficient lignin bioconversion. Lignin structural changes have been investigated in the presence of P. putida. For example, 13P NMR results revealed the β-5 phenolic group from lignin significantly decreased when Dyp was overexpressed in P. putida . 2D NMR results revealed ferulic acid and p-coumaric acid signals from lignin disappeared at 72 h of fermentation in P. putida KT2440 . Although bacterial lignin conversion examples are accumulating, most of the studies fermented the wild-type or mutated P. putida together with lignin which overlapped the function of secreted enzyme system with the strain. The specific function of extracellular enzyme systems on lignin structural change and degradation pathway is still unknown in P. putida compared to fungi cocktails [33, 36, 39].
In this study, we tracked the activity of oxidases and peroxidase/Mn2+-peroxidase in the secretome of Pseudomonas putida KT2440 that grew on glucose as the only carbon source. The active secretome was isolated to react with alkali lignin in order to measure the lignin degradation rate with or without the addition of H2O2 and Mn2+. The degraded lignin products and structural change were analyzed by GC–MS and NMR to investigate the possible reaction mechanisms of lignin degradation by secretome in P. putida KT2440. In addition, global proteomics analysis was carried out for secretome and intracellular proteome to identify potential enzymes involved in the lignin degradation process (Additional file 1: Fig. S1).
Cell growth and concentration of extracellular and intracellular protein
To generate an effective secretome with active extracellular enzymes in Pseudomonas putida, P. putida cells were first grown on M9 medium with 5 g·L−1 glucose and 1 g·L−1 NH4Cl for 8 days. The optical density (OD600) and extracellular and total protein (intracellular + extracellular) concentrations were measured.
Figure 1 depicts the cell density (OD600), and extracellular and total protein concentrations over time. As shown in Fig. 1a, with 5 g·L−1 glucose, cells grew fast for the first 72 h of fermentation, and the optical density reached 2.1 and maintained a similar level until the end of the fermentation.
A distinct pattern was revealed for protein concentration. As shown in Fig. 1b (blue line), the extracellular protein concentration reached 1.1 mg·mL−1 at 24 h and dropped to 0.6 mg·mL−1 at 48 h, then gradually increased to 0.9 mg·mL−1 at 144 h and further decreased to 0.4 mg·mL−1 at the end of fermentation. The same trend was also observed for total protein concentration (red line). The total protein concentration reached 1.2 mg·mL−1 at 24 h and dropped to 0.7 mg·mL−1 at 48 h, then gradually increased to 1.0 mg·mL−1 at 144 h and further decreased to 0.7 mg·mL−1 at the end of fermentation. The total protein concentrations were higher than the extracellular protein, including the lysate intracellular protein. These results indicated that the P. putida cells secreted protein to extracellular space and the extracellular protein concentration fluctuated over time. However, further enzyme activity assays are still required to examine whether these proteins are secreted as active form or not.
Extracellular vs. intracellular enzyme activity
P. putida cells secreted proteins to extracellular space when grown on glucose. However, whether the secretome harbors active ligninolytic enzymes still requires specific investigation. The phenolic substrate 2,6-dimethoxyphenol (DMP) is usually used to track laccase-like oxidases and peroxidase activities . Therefore, oxidases, peroxidases, and Mn2+-oxidizing peroxidases were tracked in the culture supernatants and intracellular over 8-day incubations. In Fig. 1c, extracellular oxidase activity was detected at a low level at 24 h, and gradually increased to 0.25 U/L at 120 h. In Fig. 1d, the profiles for intracellular enzymes are similar to extracellular enzymes. The oxidase activity was maintained at a low level at 24 h and then gradually increased to 0.12 U/L at 120 h.
The peroxidase activity (e.g., Dyp) was also measured with DMP and H2O2 addition . In Fig. 1c, extracellular peroxidase activity was detected at a low level at 24 h and gradually increased to 1.8 U/L at 120 h. In Fig. 1d, the profiles for intracellular enzymes are similar to extracellular enzymes. The peroxidase activity was maintained at a low level at 24 h and then gradually increased to 1.6 U/L at 120 h.
DMP was also used to measure the reaction’s Mn2+-peroxidase activity with H2O2 and Mn2+ . In Fig. 1c, extracellular peroxidase activity was detected at a low level at 24 h, and gradually increased to 2.5 U/L at 120 h. In Fig. 1d, the profiles for intracellular enzymes are similar to extracellular enzymes. The Mn2+-peroxidase activity was maintained at a low level at 24 h and then gradually increased to 1.7 U/L at 120 h.
Collectively, the results in Fig. 1c demonstrate that P. putida secreted the enzyme to the extracellular space, and the maximum enzyme activity appeared at 120 h of fermentation. The intracellular enzyme activity showed a similar pattern as extracellular in Fig. 1d, with the maximum enzyme activity at 120 h. Therefore, the extracellular enzyme at 120 h of fermentation was selected for the following lignin degradation reaction.
Amount of alkali lignin degraded
The lignin degradation reaction solution was set up with secretome and 2 g·L−1 alkali lignin with or without 0.1 mM H2O2 and 0.1 mM Mn2+ addition and reacted for 5 days. Apart from the secretome alone treatment, H2O2 and/or Mn2+ were added separately to activate the capacity of peroxidase and Mn2+-peroxidase performance on lignin degradation. In Fig. 2, when individual secretome was used for lignin degradation reaction, the amount of alkali lignin degraded only reached 8.1%, which was substantially lower than that for either H2O2 or H2O2 with Mn2+ addition. When H2O2 was added to the reaction, the amount of alkali lignin degraded reached 13.5%. With the presence of both H2O2 and Mn2+, the alkali lignin degradation rate reached a maximum value of 14.5%. On the other side, the effectiveness of H2O2 alone has also been tested for comparison, with the alkali lignin degradation rate as of 7.8% only.
GC–MS analysis of lignin breakdown products
GC–MS analysis was performed to identify the lignin breakdown products with secretome and the addition of H2O2 and Mn2+. The NIST library was used to identify and assign the chromatographic peaks. The amount of each aromatic degradation product was determined from the corresponding peak area in the chromatogram.
The GC–MS chromatogram identified aromatic compounds, furan, aldehydes, esters, organic acids, and alkanes among different samples (Additional file 2: Figs. S2–S4, and Table S1, S2). These identifications should be interpreted as unvalidated candidates; some may be incompatible with known or plausible lignin degradation mechanisms.
Peak area for all observed compounds was analyzed and shown in Additional file 1: Fig. S4, which were further separated as four groups after being compared with their alternatives in lignin control (Additional file 1: Table S2). Notably, when lignin was treated with H2O2, a wide range of aromatic monomers and dimers (No. 1, 4, 5, 6, 12, 14, 16–18, 20–21) were significantly increased. These compounds were only present in limited amounts or even not detected when treated with secretome alone or in the presence of H2O2 and Mn2+, suggesting the non-specific oxidative cleavage (e.g., H2O2) showed stronger products release ability compared to enzymatic cleavage. Moreover, the peak area of identified compounds among all the secretome treatments showed a similar distribution pattern (compounds No. 3, 7, 8, 9, 10, 13, 14, 25, 30, 31, 33) but with difference abundance, suggesting the increased compounds might be associated with different activated enzymes. For example, phenol, 2-methoxy-4-propyl- and 3-benzofurancarboxylic acid, 2,3-dihydro-2-methoxy-, methyl ester, trans- (compounds 8 and 13) were increased in secretome alone treatment and maintained the similar level or decreased by H2O2 and Mn2+ addition, indicating these products might be associated with oxidases behavior. Similarly, the peak area of phenol, 4-ethyl-2-methoxy- and acetovanillone (compounds 3 and 9) were enhanced by H2O2, and vanillic acid (compound 11) was enhanced by Mn2+ addition, suggesting these compounds might be associated with peroxidase behavior. How lignin structural changes were impacted by these treatments was further explored by NMR analysis.
2D HSQC NMR spectra from the hydrolyzed lignin
The cleavage of lignin C–O–C linkages is vital in the bacterial lignin degradation process. The quantification of each linkage is based on the volume integration of cross-peak contours in the HSQC spectra. In this study, lignin linkages such as β-O-4, β-β, β-5, and β-1 were cleaved with H2O2 or secretome treatments (Fig. 3a–j, Table 1 and Additional file 1: Fig. S5, Table S3). As shown in Table 1, in general, the cleavage of β-5 was less extensive than the cleavages of β-O-4, β-β, and β-1, which indicated that β-5 bonds were relatively more stable. The cleavage of these linkages was increased when lignin was treated with H2O2. Among all the detected linkages, β-O-4 bonds exhibited the most extensive cleavage, demonstrating the non-enzymatic chemical reaction with H2O2 mainly cleavage β-O-4 bonds. In contrast, when lignin was treated with secretome alone, β-O-4 bonds only exhibited limited cleavage compared to that with H2O2. While the cleavage of β-β, β-5, and β-1 showed increased cleavage compared to that with H2O2, suggesting the secretome alone may only exhibit oxidase ability and cleavage the C–C bond. When introducing the H2O2 with the secretome, β-O-4 bonds were extensively decreased, β-β and β-1 were further decreased compared to secretome alone. Hydrogen peroxide activates the peroxidase and further cleavages the β-O-4 bonds. In addition, the presence of Mn2+ further enhanced the peroxidase performance and resulted in further enhanced β-O-4, β-β and β-1 bonds cleavage.
Secretome and cellular proteome profiles in P. putida
GC–MS and NMR results demonstrated that P. putida secretome is able to depolymerize lignin. Enzyme assay revealed that the secretome exhibited the oxidase and peroxidase activity. However, isoenzymes with similar activities cannot be distinguished based on simple activity analysis. To deeply characterize the secretome, mass spectrometry-based global proteomics was utilized to profile the proteome of secretome and intracellular extracts in P. putida KT2440. Bacterial secretome and cell pellet were harvested at 120 h of fermentation with the highest oxidase and peroxidase activity. Only those proteins presented in more than three replicates were considered as reliable detection and quantitation. Results showed that 1312 proteins were identified in the secretome sample, which was lower than that in the intracellular extracts for 2388 identified proteins. Around 94.8% of the secretome proteins were shared with the intracellular protein, and only 68 proteins were exclusively detected in the secretome (Fig. 4a).
Secretome proteins were then organized by function and presented in Fig. 4b. Despite the other function and unknown function groups, the oxidoreductase group was the most abundant among the rest of the functional groups, which accounted for 14.1% in secretome proteome. Moreover, six glutathione S-transferases were detected and grouped in the transferase group. A deeper analysis of oxidoreductase is presented in Fig. 4b as well. The dehydrogenase group was the most abundant (42.2%), followed by reductase (17.3%), peroxidase (7.6%), oxidase (6.5%), monooxygenase (4.9%), and dioxygenase (2.2%). Notably, there are 14 peroxidases detected, such as Dyp-type peroxidase (PP_3248), cytochrome c551 peroxidase (PP_2943), and alkyl hydroperoxide reductase (e.g., ahpC). Besides, 12 oxidases were detected, including three multicopper oxidases (copA/B and CumA). Besides, a couple of dehydrogenases were detected in the secretome, including NAD(P)H dehydrogenase (e.g., PP_1644), choline dehydrogenase (e.g., betA), aldehyde dehydrogenase (e.g., aldB-I), and alcohol dehydrogenase(e.g., PP_2827). In addition, some hydrogen peroxide alleviating enzymes were also detected, such as catalase (e.g., katG), superoxide dismutase (sodB), and thioredoxin (e.g., trx). Overall, proteomics analysis revealed the oxidoreductase enzymes in the secretome, which not only confirmed the enzyme assay results, but also revealed the specific ability to selectively depolymerize lignin.
Lignin degradation pathways of P. putida secretome
Based on the enzyme activity analysis, GC–MS, NMR, proteomics results, the proposed lignin degradation reaction pathways are shown in Fig. 5 [21, 27, 37, 40,41,42,43,44,45,46]. The enzymes identified that might be involved in the lignin catabolism pathway are summarized in Additional file 2: Table S4. Overall, the proposed lignin degradation pathways include cleavage of β-aryl ether (β-O-4), resinol (β-β), phenylcoumaran (β-5), and spirodienone (β-1) linkages. Figure 5 demonstrates that vanillin (compound 7) and vanillic acid (compound 11) are the most important intermediates for all these linkages.
Limited β-O-4 bond cleavage (Table 1) was observed when lignin was treated with secretome alone, possibly catalyzed by the NAD(P)H dehydrogenases (similar to LigD/N/L in Sphingobium sp. SYK-6)  and multicopper oxidase (e.g., CopA) in the enzyme system through α-OH oxidation and Cα-Cβ cleavage forming vanillic acid (compound 11). Besides, proteomics results also revealed that glutathione S-transferases (GST), glutathione reductases (gor), and choline dehydrogenase (betA) were presented in the secretome, which functioned as LigE/F, LigG, and HpvZ in Sphingobium sp. SYK-6 [42, 44, 47]. Thus, in parallel to the multicopper oxidase route, oxidized β-O-4 linkage could also be converted to vanillic acid with the assist from GST, betA, and gor. In addition, NMR results revealed that the presence of H2O2 with secretome and lignin enhanced the β-O-4 cleavage and GC–MS demonstrated the peak abundance of vanillic acid (compound 11) increased with the H2O2 and Mn2+ addition. Proteomics results detected the Dyp-type peroxidase (PP_3248) in the secretome. Therefore, the β-O-4 linkage was degraded by Dyp-type peroxidase, forming vanillic acid as the degradation product (Fig. 5).
NMR results revealed the presence of secretome alone with lignin degraded the resinol linkage (β-β). Based on the homologous alignment of the amino acid sequence in NCBI database (blastp), FAD-binding oxidoreductase (PP_5154) exhibited the 62.8% similarity to pinoresinol α-hydroxylase in Pseudomonas sp. SG-MS2 . Therefore, resinol linkage might be converted to vanillin and vanillic acid by FAD-binding oxidoreductase (Fig. 5). Besides, the addition of H2O2 stimulated the resinol linkage cleavage, suggesting the peroxidase might be involved in β-β bond degradation. Therefore, peroxidase might be involved in the resinol linkage cleavage and forming vanillic acid as the intermediate (Fig. 5).
NMR results revealed the presence of secretome alone with lignin degraded the phenylcoumaran linkage (β-5). Notably, choline dehydrogenase (betA) exhibited 40% of similarity to phcC/D in Sphingobium sp. SYK-6 based on blastp analysis in NCBI for P. putida KT2440 [44, 49, 50]. Proteomics results demonstrated the aldehyde dehydrogenase (aldA/aldB-I) presented in P. putida secretome (Additional file 2: Table S4). However, lignostilbene α,β-dioxygenase (lsdD) in Sphingobium sp. SYK-6 did not exhibit the homology protein in P. putida after the blast analysis. There might be other degradation mechanisms in P. putida KT2440 for stilbene structure which require future investigation. Therefore, β-5 linkage degradation pathway of P. putida KT2440 is only partially consistent with the route of Sphingobium sp. SYK-6 (Fig. 5) [44, 49, 50]. In addition, the presence of H2O2 only slightly increased the β-5 linkage compared to secretome alone, suggesting the peroxidase might not involve in β-5 cleavage.
NMR results demonstrated the secretome alone contributed to spirodienone linkage cleavage, suggesting the β-1 bond cleavage capacity in the secretome. NCBI blast revealed there was no homologous protein for lsdE and lsdA in P. putida KT2440 .Therefore, there might be other mechanisms for β-1 linkage in P. putida. Besides, the presence of H2O2 stimulating the β-1 cleavage, and Mn2+ addition further enhanced β-1 cleavage, suggesting the peroxidase might be involved in β-1 cleavage as well. Therefore, the β-1 linkage degradation pathway for P. putida KT2440 is presented in Fig. 5.
Overall, the extracellular lignin degradation mechanism has been revealed by P. putida KT2440 via secretomic analysis. The enzymatic assay demonstrated that the secretome contains active oxidase and peroxidase. The following lignin degradation rate analysis proved that the secretome could degrade 8.6% of the lignin, and the addition of H2O2 and Mn2+ would increase the lignin degradation rate to 14.5%. C–C bond cleavage was observed by 2D NMR in secretome alone treatment, and β-O-4 bond and C–C bond (β-β and β-1) cleavage were elevated when H2O2 was introduced to secretome due to the activated peroxidase system. Further Mn2+ addition enhanced β-O-4 and C–C bond (β-β and β-1) cleavage. GC–MS results reinforced the NMR results by demonstrating elevated peak areas of aromatic monomers, such as vanillin and vanillic acid were correlated with C–C and C–O bonds cleavage. Proteomics results revealed the different groups of oxidoreductases involved in lignin degradation, and the degradation pathways were proposed.
The bacterial lignin degradation process requires extensive reducing power and energy to cope with the polymeric structure and corresponding oxidative stress during aromatic compound catabolism . Therefore, many studies chose to co-fermentation lignin with nutrient-rich substrates like glucose [17, 33, 35, 51]. Our results demonstrated that the secretome harbored active oxidase, suggesting the presence of multicopper oxidase in secretome generated from P. putida grown on glucose. Moreover, active peroxidase was also observed in secretome, suggesting that besides Dyp-type peroxidase, other potential peroxidases are also involved in lignin catabolism. Proteomics analysis revealed that the secretome contained multicopper oxidase (CopA) and Dyp-type peroxidase (PP_3248) and presented abundant oxidoreductase enzymes. Therefore, our results demonstrated that P. putida also secreted active ligninolytic enzymes into extracellular space when grown on nutrient-rich media (e.g., glucose).
Our results showed that secretome alone exhibited limited lignin degradation capacity, which was lower than in the P. putida KT2440 strain. Moreover, our results further demonstrated that the addition of H2O2 and Mn2+ can activate peroxidases and increase lignin degradation, suggesting that the synergistic effect between bacteria and the enzyme system could be enhanced through chemical addition on lignin degradation. H2O2 is the oxidant and electron acceptor for bacterial peroxidase during the enzymatic reaction. Purified dye-decoloring peroxidase from Rhodococcus and Pseudomonas (e.g., Rh_Dyp, and PpDyp) revealed that the addition of Mn2+ in the presence of H2O2 further enhanced the enzyme activity [31, 52,53,54]. These results point to an alternative way to enhance the bacterial lignin bioconversion efficiency by introducing H2O2 and Mn2+ to work together with the enzyme system and bacteria cells.
NMR results showed secretome alone presented extensive C–C bond cleavage and limited C–O bond cleavage, suggesting the function of oxidases in the secretome. Bacteria oxidases (e.g., multicopper oxidase) are laccase-like oxidase and exhibit the C–C bond cleavage. Our results demonstrated that vanillic acid (compound 11) peak area was presented in secretome + lignin treatments (Additional file 1: Fig. S4), suggesting the involvement of multicopper oxidases in lignin degradation through Cα–Cβ cleavage .
The addition of H2O2 with secretome elevated the β-O-4 bond cleavage of lignin which might be attributed to the activation of dye-decoloring peroxidase (Dyp) (Table 1). Our results identified the syringaldehyde like compounds such as phenol, 2,6-dimethoxy-4-(2-propenyl)- (compound 14) and ethanone, 1-(4-hydroxy-3,5-dimethoxyphenyl)- (compound 16), which were presented limited amount in secretome treatments but elevated when lignin was treated with H2O2. Besides, our results showed the phenolic products (compounds 3 and 9) were elevated when H2O2 was presented with secretome, suggesting the possible non-enzymatic cleavage for the phenolic type of β-O-4 bond .
NMR results also revealed secretome alone presented a series of C–C bond cleavages including β-β, β-5, and β-1 (Table 1 and Fig. 5). Our results revealed the β-β linkage was initially catalyzed via α-hydroxylation by vanillyl alcohol oxidase/p-cresol methyl hydroxylase (VAO/PCMH) like enzyme (PP_5154), forming vanillin and vanillic acid as the intermediate compounds during the degradation process [48, 55]. Our results showed β-5 linkage was cleavage by choline dehydrogenase (betA) and aldehyde dehydrogenase (aldA/aldB-I) which was partially consistent with literature . In addition, no homologous proteins for lsdE and lsdA were found in P. putida KT2440 showed there might be a different β-1 linkage breakdown mechanism compared to Gram-negative bacteria Novosphingobium aromaticivorans DSM12444 .
Apart from the compounds that were confirmed by previous literature, we also identified some aromatic dimer compounds in different treatments. For example, [1,1'-biphenyl]-3,3'-dicarboxaldehyde, 6,6'-dihydroxy-5,5'-dimethoxy- (compound 30) which might be correlated with 5–5’ linkage cleavage and 3-(4-acetoxy-3-methoxyphenyl)-7-methoxy-4-oxo-4H-chromene (compound 26) might be related to tricin cleavage. However, more compounds were not correlated with specific reaction mechanisms that showed more reactions in the lignin degradation process. Our results also demonstrated inconsistency in secretome treatments with a lower aromatic compound release but larger linkage cleavage than H2O2 treatment, implying the low aromatic compounds released might be another bottleneck in the bacterial lignin degradation process. Future studies can focus on engineering oxidative degradation enzymes towards a higher aromatic compounds release.
Proteomics-guided systems-biology approaches have been proven to discover potential pathways involved in lignin catabolism effectively . Previously Dyp only reportedly appeared overexpressed in exoproteome of P. putida from the lignin-rich media . However, our secretomic analysis revealed that Dyp, SOD, CopA, and other accessory enzymes such as catalase, dehydrogenases, reductases, dioxygenases, and oxidases all existed in the secretome from glucose which was different from the previously reported lignin inducing hypothesis. Overall, the extracellular lignin degradation pathways by P. putida are not well understood, primarily due to their broad prospects under varied environmental conditions [21, 27, 37, 40,41,42,43,44,45,46]. This distinctive study provided detailed information on lignin degradation products and oxidoreductase enzymes, resulting in new insights into the lignin depolymerization pathways in P. putida KT2440 for future metabolic engineering design to improve lignin bioconversion efficiency.
In summary, based on enzyme assay, GC–MS, NMR, and proteomics analysis, the extracellular lignin degradation mechanisms of the secretome from P. putida KT2440 were elucidated as follows: (1) oxidase (e.g., multicopper oxidase, CopA) exhibited limited β-Ο-4 bond cleavage capacity; (2) peroxidase (e.g., dye-decoloring peroxidase, DyP) was activated by H2O2 and enhanced by Mn2+ addition, stimulating the β-Ο-4, β-β, and β-1 bond cleavage; (3) degradation reaction mechanisms involved in Cα–Cβ cleavage, Cα-oxidation, Cα-hydroxylation, followed by aromatic intermediates release (e.g., vanillin and vanillic acid); (4) abundant oxidoreductase enzymes in P. putida secretome participated in lignin degradation. To be specific, Dyp-type peroxidase, multicopper oxidase, NAD(P)H dehydrogenase, glutathione reductase, glutathione S-transferase, and choline dehydrogenase participated in β-Ο-4 bond cleavage. Results showed that FAD-binding oxidoreductase involved in β-β bond cleavage, choline dehydrogenase and aldehyde dehydrogenase involved in β-5 bond cleavage, and peroxidases involved in β-β and β-1 bond cleavage. Overall, our study provides a comprehensive understanding and list of functional enzymes of the extracellular lignin degradation pathway in P. putida KT2440 in order to build a roadmap for future metabolic engineering design to improve the efficiency of lignin bioconversion. Further research can be carried out to overexpress identified functional proteins for specific lignin degradation mechanism studies.
Microorganism and medium
Pseudomonas putida KT2440 was purchased from American Type Culture Collection (ATCC 47054) and stored in 25% glycerol at − 80 °C. All the chemical reagents were purchased from Sigma Aldrich and Fisher Scientific with ACS grade (99% purity). The composition of M9 mineral medium was as follows: 6 g·L−1 Na2HPO4, 5 g·L−1 glucose, 3 g·L−1 KH2PO4, 1 g·L−1 NH4Cl, 0.5 g·L−1 NaCl, 0.12 g·L−1 MgSO4 and 1 mL·L−1 1000-fold trace element mix solution to make the final concentrations as follows: 3 μM (NH4)6Mo7O24·4H2O, 0.4 mM H3BO3, 30 μM CoCl2·6H2O, 10 μM CuSO4·5H2O, 80 μM MnCl2·4H2O, 10 μM ZnSO4·7H2O, 1 μM FeSO4·7H2O [38, 58, 59].
Protein concentration measurement
1 mL of fermentation broth was taken from each M9 medium culture every 24 h of fermentation with two replicates. The supernatant was separated by centrifuge at 8014 g (8000 rpm) for 5 min. Parallelly, another 1 mL cell culture was taken from each M9 medium for total protein measurement. Cell cultures were frozen at -80 °C for 15 min at first. The cell suspension was taken into a water bath (42 °C) for 5 min and repeated the freeze–thaw cycle three times. The supernatant and total protein concentrations were estimated by the Pierce™ BCA protein assay kit (Thermo Scientific, San Jose, CA).
Ligninolytic activity assays for intracellular and secretome
A 1 mL cell culture was taken from each M9 medium culture at different fermentation times and stored in a 1.5-mL centrifuge tube for total enzyme activity assay measurement (intracellular + secretome) with two replicates. Cell cultures were frozen under -80 °C for 15 min at first. The cell suspension was taken into a water bath (42 °C) for 5 min and repeated the freeze–thaw cycle three times. Another 1 mL cell culture was also taken from each M9 medium culture and centrifuged at 8000 rpm for 5 min. Then, the supernatant was transferred to a new 1.5-mL centrifuge tube for secretome enzyme activity assay measurement. Laccase and peroxidase activity were examined daily in the culture supernatants by the oxidation of 5 mM DMP (synonym syringol) to dimeric cerulignone (ε469 = 55 000 M−1 cm−1) in 0.1 mM sodium malonate buffer at pH 7. For peroxidase activity assays, 0.1 mM H2O2 was also added to initiate the reaction. In addition, the latter assays were performed in the absence and the presence of Mn2+ (0.1 mM MnSO4). Absorbance from peroxidase activity was corrected with that caused by laccase activity. Measurements were carried out at room temperature. One unit (1 U) of activity is defined as the amount of enzyme releasing 1 μmol of product per minute under the defined reaction conditions .
P. putida strains were fed in 100 mL M9 medium in a 250-mL flask with 5 g·L−1 glucose and 1 g·L−1 NH4Cl for 5 days. The fermentation broth was transferred to a couple of 50 mL centrifuge tubes. The supernatant and cells were separated by centrifugation at 8014 g (8000 rpm) for 5 min. The supernatant was transferred to a new pre-cooled flask (1 L) in ice batch. The supernatant was centrifuged again at 8014 g (8000 rpm) for 5 min and then passed through 0.22 μm sterilized filter (Millipore® Stericup® filtration system) to a new flask (1 L) for further degradation experiment. Ligninolytic enzyme activities and protein concentration were measured prior to the lignin degradation reaction.
Lignin degradation reaction with secretome
Corn stover alkali lignin was purified following a published methodology (more details about the alkali lignin purifying process, composition and structural analysis can be found elsewhere) . A fresh stock alkali lignin solution (20 g·L−1) was prepared at pH 12.5 and then adjusted to pH 7. 250 mL Erlenmeyer flasks with 50 mL of lignin degradation reaction solution were cultivated in a shaking incubator at 180 rpm and set to 37 °C. The basic composition of lignin degradation reaction solution (50 mL) was as follows: secretome solution 45 mL, lignin stock solution 5 mL (100 mg, final concentration 2 g·L−1), and sodium malonate 0.1 mM. The reaction solution was also supplemented with H2O2 (0.1 mM) and Mn2+ (0.1 mM) to evaluate their effect on lignin degradation together with secretome. The secretome or lignin control contained 45 mL secretome solution with 5 mL Milli-Q water or 5 mL lignin stock solution with 45 mL Milli-Q water. Every treatment was a set of three replicates with a total of 18 flasks.
The reaction was stopped after 120 h, and the reaction solution was transferred to a 50-mL centrifuge tube. The lignin amount determination followed NREL Laboratory Analytical Procedures (LAPs) [61, 62]. The reaction solution was first adjusted pH to 2 by adding the hydrochloric acid (1 mol·L−1). The acid-insoluble lignin was harvested by centrifugation at 8014 g (8000 rpm) for 5 min. The supernatant was carefully transferred to a new 50 mL centrifuge tube for degradation products analysis. The acid-insoluble lignin was freeze-dried and weighed. The acid-insoluble lignin from secretome treatments was corrected with the acid-precipitated and weighed secretome control to remove the protein amount. The lignin degradation rate was indicated as the difference between the remaining lignin after different treatments and control, followed by dividing the control .
Analysis of lignin degradation products
The lignin degradation products in the reaction solution were determined by gas chromatography–mass spectroscopy (GC–MS). Every treatment was a set of three replicates. 15 mL of ethyl acetate was added to 15 mL solutions from the different samples in a 50-mL centrifuge tube and was vortexed for 5 min at room temperature. The top ethyl acetate layer was then transferred to a glass tube. The remained reaction solution was extracted again with 15 mL ethyl acetate and the two extracts were merged. The glass tubes were left in the fume hood for 7 days to let the ethyl acetate evaporate naturally to around 2 mL. The ethyl acetate was concentrated to around 1 mL by passing nitrogen for 20 min and then filtered with 0.45 μm PTFE membrane into the GC vials . The organic solvent-extracted samples (1 μL) were injected into a stream of He (carrier gas) flowing at 1.2 mL·min−1 into a DB5 (30 m × 0.250 μm × 0.25 μm) capillary column fitted in an Agilent Technologies 7890A GC system set in the splitless mode. The GC oven was programmed to reach 45 °C and maintained this temperature for 2 min; then ramp up at the rate of 15 °C min−1 until the temperature reached 200 °C, and held at this temperature for 1 min, after which the temperature was increased at a rate of 5 °C min−1 until the temperature reached 280 °C. At this temperature, it was held for 7 min. Eluting compounds were detected with an MS (Agilent Technologies 5975C) inert XL EI/CI MSD with a triple-axis detector and compared using NIST libraries .
2D HSQC NMR analysis
2D-1H–13C heteronuclear single-quantum coherence (HSQC) nuclear magnetic resonance (NMR) spectra were obtained using a Bruker Avance III HD 500 MHz spectrometer operating at a frequency of 125.12 MHz for the 13C nucleus. 30–50 mg of the dry lignin samples were dissolved in 0.6 mL deuterated dimethylsulfoxide (DMSO)-d6 and the spectra were collected at 298 K. A standard Bruker adiabatic HSQC pulse sequence (hsqcetgpsisp2.2) was used with the following spetra acquisition condition: 1.0 s pulse delay, 64 scans, 1024 data points for 1H, 256 increments for 13C, and a 1JC–H of 145 Hz. The 1H and 13C spectral widths are 13.0 and 220.0 ppm, respectively. The central DMSO solvent peak (δ13C/δ1H = 39.5/2.49 ppm) was used for chemical shifts calibration. HSQC spectra were processed and analyzed with Mestrenova (version 12.0.2) with a matched cosine-bell apodization and 2 × zero filling in both dimensions. The content of the inter-linkages are expressed as a percentage relative to the total lignin subunits (G + H + S) .
Protein extraction and tryptic digestion
P. putida strains were fed in 100 mL M9 medium in a 250 mL flask with 5 g·L−1 glucose and 1 g·L−1 NH4Cl. The experiment was conducted with four replicates. The cells and supernatant were harvested at 120 h of fermentation. The fermentation broth was centrifuged at 8014 g (8000 rpm) for 5 min using Eppendorf 5804 to separate the supernatant and cell pellet. The cell pellet was washed twice with 5 mL of 0.9% sodium chloride solution. The supernatant was filtered with 0.22-μm PTFE membrane into new 50-mL centrifuge tubes. Cell pellet and supernatant were stored at − 80 °C fridge for further protein extraction.
Cell pellets were stored in regular 1.5-mL centrifuge tubes. Cell pellets were resuspended in a 250 μL lysis buffer solution (8 M urea, 75 mM NaCl in 100 mM NH4HCO3, pH 7.8), transferred to a 1.5-mL safe-lock centrifuge tube. A scoop of zirconia/silica beads (~ 100 μL) was added to each tube, and the bead beating experiment was performed by 8 rounds of 30 s using a Bullet Blender (Homogenizers, Atkinson, NH) . After bead beating, a needle was used to poke a hole at the bottom of the 1.5-mL tube and put on a 15-mL falcon tube to collect the supernatant by centrifugation at 2000 rpm, 4 °C for 5 min. The beads were then washed with 100 µL lysis buffer and centrifuged at 2000 rpm at 4 °C for 5 min. The lysate was then transferred to a new 2-mL centrifuge tube and pellet the cellular debris at 14,000 rpm for 10 min at 4 °C. The supernatant was transferred to a new 2-mL centrifuge tube for further protein digestion procedures.
Parallelly, 20 mL of supernatant was collected, and the proteins were first denatured by adding 15 g urea (final concentration 8 M) and incubating for 1 h at 37 °C. The supernatant was then concentrated using a 30-kDa filter (EMD Millipore, Billerica, MA) by centrifugation at 4000 rpm, 4 °C for 30 min. The concentrated supernatant was transferred to a clean 2-mL tube for further protein digestion procedures.
The protein purification and digestion of intracellular protein and supernatant samples were conducted with the FASP Protein Digestion Kit (Expedeon, San Diego, CA) with trypsin (Promega, Madison, WI) following the manufacturer’s instruction. The protein concentration was estimated by the Pierce™ BCA protein assay (Thermo Scientific, San Jose, CA) and normalized to 0.1 μg μL−1 before LC–MS/MS analysis. Four biological replicates were applied during the entire process .
Proteomic data acquisition and analysis
LC–MS/MS analysis was performed using an Orbitrap Fusion Lumos mass spectrometer (Thermo Scientific, San Jose, CA). Tryptic peptide digests were separated using a nanoACQUITY UPLC systems (Waters, Milford, MA) by reversed-phase HPLC with 110 min gradient time at a column flow rate of 200 nL/min. The detailed equipment parameters setup was described in a recent publication by Wang et al.  In terms of proteomic data analysis, raw MS/MS data files were processed with MaxQuant (version 220.127.116.11). After loading all the raw data and giving appropriate names, label-free quantification (LFQ) algorithm was used with a minimum LFQ ratio count of 2 for relative quantification in the Group-specific parameters section. Trypsin was selected for digestion mode with a maximum of two missed cleavages. The peptide tandem mass spec raw data were searched against the Uniport FASTA files of strain P. putida KT2440 (released at 07, April 2017, Taxonomy ID: 160488). In the global parameters section, the second peptides and match between runs features were enabled with a 0.7-min match time window and 20-min alignment time window. The spectral level false discovery rate (FDR, q value) was < = 1% based on a decoy search . Other parameters just followed the default settings. The protein intensities obtained from Maxquant software were log2 transformed. The Venn chart was generated by Venn-Diagram-Plotter (version 1.6.7458, https://github.com/PNNL
-Comp-Mass-Spec/Venn-Diagram-Plotter/releases/tag/v1.6.7458). Pie chart was generated by Origin software (version 18.104.22.168).
Availability of data and materials
All data generated or analyzed during this study are included in this published article and its supplementary information files.
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A portion of the research was performed using EMSL (grid.436923.9), a DOE Office of Science user facility sponsored by the Biological and Environmental Research program. Oak Ridge National Laboratory is managed by UT-Battelle, LLC under Contract DE-AC05-00OR22725 with the U.S. Department of Energy (DOE). The proteomics experimental work described herein was performed in the EMSL, Pacific Northwest National Laboratory, a national scientific user facility sponsored by the United States of America Department of Energy under Contract DE-AC05-76RL0 1830. The authors would like to thank Ms. Kendall Martin and Dr. Xiaolu Li from the Pacific Northwest National Laboratory for insightful discussions. The views and opinions of the authors expressed herein do not necessarily state or reflect those of the United States Government or any agency thereof. Neither the United States Government nor any agency thereof, nor any of their employees, makes any warranty, expressed or implied, or assumes any legal liability or responsibility for the accuracy, completeness, or usefulness of any information, apparatus, product, or process disclosed, or represents that its use would not infringe privately owned rights. The US government retains and the publisher, by accepting the article for publication, acknowledges that the US government retains a nonexclusive, paid-up, irrevocable, worldwide license to publish or reproduce the published form of this manuscript, or allow others to do so, for US government purposes. DOE will provide public access to these results of federally sponsored research in accordance with the DOE Public Access Plan (http://energy.gov/downloads/doe-public-access-plan).
This work is supported by the U.S. Department of Energy (DOE), the Office of Energy Efficiency & Renewable Energy (EERE) Awards (DE-EE0007104, DE-EE0006112, and DE-EE0008250), NIH R01GM139858 (to T.S.), and the Bioproducts, Science and Engineering Laboratory, Department of Biological Systems Engineering at Washington State University. Y.P. and A.R. were partially supported by the Center for Bioenergy Innovation (CBI), a Department of Energy Bioenergy Research Center supported by the Office of Biological and Environmental Research in the DOE Office of Science. Z.X. is grateful for the support from the Pacific Northwest National Laboratory (PNNL)-Washington State University (WSU) Distinguished Graduate Research Program (DGRP) Fellowship.
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The overall workflow for identifying bacterial lignin degradation pathways. Figure S2. GC–MS analysis of lignin breakdown products. Figure S3. Lignin breakdown products identified by GC–MS. Figure S4. The variation of peaks area of all lignin breakdown products. Figure S5. Main detected lignin linkages. Table S1. Occurrence of putative degradation products of lignin in different treatment conditions. Table S2. Grouped lignin breakdown products among all treatments. Table S3. Main lignin 2D 1H–13C Cross-peak assignments in the HSQC Spectra.
Proteomic analysis of the intracellular and secretome in P. putida KT2440.
A list of abbreviations is included.
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Xu, Z., Peng, B., Kitata, R.B. et al. Understanding of bacterial lignin extracellular degradation mechanisms by Pseudomonas putida KT2440 via secretomic analysis. Biotechnol Biofuels 15, 117 (2022). https://doi.org/10.1186/s13068-022-02214-x
- Lignin degradation
- Pseudomonas putida