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Overexpression of ferulate 5-hydroxylase increases syringyl units in Sorghum bicolor

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Abstract

Ferulate 5-hydroxylase (F5H) of the monolignol pathway catalyzes the hydroxylation of coniferyl alcohol, coniferaldehyde and ferulic acid to produce 5-hydroxyconiferyl moieties, which lead to the formation of sinapic acid and syringyl (S) lignin monomers. In contrast, guaiacyl (G) lignin, the other major type of lignin monomer, is derived from polymerization of coniferyl alcohol. In this study, the effects of manipulating S-lignin biosynthesis in sorghum (Sorghum bicolor) were evaluated. Overexpression of sorghum F5H (SbF5H), under the control of the CaMV 35S promoter, increased both S-lignin levels and the ratio of S/G lignin, while plant growth and development remained relatively unaffected. Maüle staining of stalk and leaf midrib sections from SbF5H overexpression lines indicated that the lignin composition was altered. Ectopic expression of SbF5H did not affect the gene expression of other monolignol pathway genes. In addition, brown midrib 12-ref (bmr12-ref), a nonsense mutation in the sorghum caffeic acid O-methyltransferase (COMT) was combined with 35S::SbF5H through cross-pollination to examine effects on lignin synthesis. The stover composition from bmr12 35S::SbF5H plants more closely resembled bmr12 stover than 35S::SbF5H or wild-type (WT) stover; S-lignin and total lignin concentrations were decreased relative to WT or 35S::SbF5H. Likewise, expression of upstream monolignol biosynthetic genes was increased in both bmr12 and bmr12 35S::SbF5H relative to WT or 35S::SbF5H. Overall, these results indicated that overexpression of SbF5H did not compensate for the loss of COMT activity.

Key message

Overexpression of F5H in sorghum increases S-lignin without increasing total lignin content or affecting plant growth, but it cannot compensate for the loss of COMT activity in monolignol synthesis.

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References

  • Boerjan W, Ralph J, Baucher M (2003) Lignin biosynthesis. Annu Rev Plant Biol 54:519–546

    CAS  PubMed  Google Scholar 

  • Bout S, Vermerris W (2003) A candidate-gene approach to clone the sorghum Brown midrib gene encoding caffeic acid O-methyltransferase. Mol Genet Genomics 269:205–214

    CAS  PubMed  Google Scholar 

  • Chapple C, Vogt T, Ellis BE, Somerville CR (1992) An Arabidopsis mutant defective in the general phenylpropanoid pathway. Plant Cell 4(11):1413–1424

    CAS  PubMed  PubMed Central  Google Scholar 

  • Chen F, Dixon RA (2007) Lignin modification improves fermentable sugar yields for biofuel production. Nat Biotechnol 25:759–761

    CAS  PubMed  Google Scholar 

  • Cherney J, Cherney D, Akin D, Axtell J (1991) Potential of brown-midrib, low-lignin mutants for improving forage quality. In: Advances in agronomy. Elsevier, Amsterdam, pp 157–198

  • Crocker EC (1933) Maule lignin test on podocarpus wood. Bot Gaz 95:168–171

    Google Scholar 

  • Dien BS, Sarath G, Pedersen JF, Sattler SE, Chen H, Funnell-Harris DL, Nichols NN, Cotta MA (2009) Improved sugar conversion and ethanol yield for forage sorghum (Sorghum bicolor L. Moench) lines with reduced lignin contents. Bioenergy Res 2:153–164

    Google Scholar 

  • Eudes A, Dutta T, Deng K, Jacquet N, Sinha A, Benites VT, Baidoo EEK, Richel A, Sattler SE, Northen TR, Singh S, Simmons BA, Loque D (2017) SbCOMT (Bmr12) is involved in the biosynthesis of tricin-lignin in sorghum. PLoS ONE 12:e0178160

    PubMed  PubMed Central  Google Scholar 

  • Franke R, Mcmichael CM, Meyer K, Shirley AM, Cusumano JC, Chapple C (2000) Modified lignin in tobacco and poplar plants over-expressing the Arabidopsis gene encoding ferulate 5-hydroxylase. Plant J 22:223–234

    CAS  PubMed  Google Scholar 

  • Godin B, Nagle N, Sattler S, Agneessens R, Delcarte J, Wolfrum E (2016) Improved sugar yields from biomass sorghum feedstocks: comparing low-lignin mutants and pretreatment chemistries. Biotechnol Biofuels 9:251

    PubMed  PubMed Central  Google Scholar 

  • Guo D, Chen F, Wheeler J, Winder J, Selman S, Peterson M, Dixon RA (2001) Improvement of in-rumen digestibility of alfalfa forage by genetic manipulation of lignin O-methyltransferases. Transgenic Res 10:457–464

    CAS  PubMed  Google Scholar 

  • Hatfield RD, Rancour DM, Marita JM (2017) Grass cell walls: a story of cross-linking. Front Plant Sci 7:2056

    PubMed  PubMed Central  Google Scholar 

  • Hill-Ambroz KL, Weeks JT (2001) Comparison of constitutive promoters for sorghum [Sorghum bicolor (L.) Moench] transformation. Cereal Res Commun 29:17–24

    CAS  Google Scholar 

  • Humphreys JM, Hemm MR, Chapple C (1999) New routes for lignin biosynthesis defined by biochemical characterization of recombinant ferulate 5-hydroxylase, a multifunctional cytochrome P450-dependent monooxygenase. Proc Natl Acad Sci USA 96:10045–10050

    CAS  PubMed  Google Scholar 

  • Huntley SK, Ellis D, Gilbert M, Chapple C, Mansfield SD (2003) Significant increases in pulping efficiency in C4H–F5H-transformed poplars: improved chemical savings and reduced environmental toxins. J Agric Food Chem 51:6178–6183

    CAS  PubMed  Google Scholar 

  • Jorgenson LR (1931) Brown midrib in maize and its linkage relations. J Am Soc Agron 23:549–557

    Google Scholar 

  • Jouanin L, Goujon T, De Nadaï V, Martin M-T, Mila I, Vallet C, Pollet B, Yoshinaga A, Chabbert B, Petit-Conil M, Lapierre C (2000) Lignification in transgenic poplars with extremely reduced caffeic acid O-methyltransferase activity. Plant Physiol 123:1363–1374

    CAS  PubMed  PubMed Central  Google Scholar 

  • Jung HG, Deetz DA (1993) Cell wall lignification and degradability. In: Jung HG, Buxton DR, Hatfield RD, Ralph J (eds) Forage cell wall structure and digestibility. American Society of Agronomy Crop Science Society of America, Soil Science Society of America, Madison, pp 315–346

    Google Scholar 

  • Lee DK, Aberle E, Anderson EK, Anderson W, Baldwin BS, Baltensperger D, Barrett M, Blumenthal J, Bonos S, Bouton J, Bransby DI, Brummer C, Burks PS, Chen C, Daly C, Egenolf J, Farris RL, Fike JH, Gaussoin R, Gill JR, Gravois K, Halbleib MD, Hale A, Hanna W, Harmoney K, Heaton EA, Heiniger RW, Hoffman L, Hong CO, Kakani G, Kallenbach R, Macoon B, Medley JC, Missaoui A, Mitchell R, Moore KJ, Morrison JI, Odvody GN, Richwine JD, Ogoshi R, Parrish JR, Quinn L, Richard E, Rooney WL, Rushing JB, Schnell R, Sousek M, Staggenborg SA, Tew T, Uehara G, Viands DR, Voigt T, Williams D, Williams L, Wilson LT, Wycislo A, Yang Y, Owens V (2018) Biomass production of herbaceous energy crops in the United States: field trial results and yield potential maps from the multiyear regional feedstock partnership. GCB Bioenergy 10:698–716

    Google Scholar 

  • Li M, Pu Y, Ragauskas AJ (2016) Current understanding of the correlation of lignin structure with biomass recalcitrance. Front Chem 4:45

    PubMed  PubMed Central  Google Scholar 

  • Meyer K, Shirley AM, Cusumano JC, Bell-Lelong DA, Chapple C (1998) Lignin monomer composition is determined by the expression of a cytochrome P450-dependent monooxygenase in Arabidopsis. Proc Natl Acad Sci USA 95:6619–6623

    CAS  PubMed  Google Scholar 

  • Mitchell R, Schmer M, Anderson W, Jin V, Balkcom K, Kiniry J, Coffin A, White P (2016) Dedicated energy crops and crop residues for bioenergy feedstocks in the central and eastern USA. Bioenergy Res 9:384–398

    Google Scholar 

  • Odell JT, Nagy F, Chua N-H (1985) Identification of DNA sequences required for activity of the cauliflower mosaic virus 35S promoter. Nature 313:810–812

    CAS  PubMed  Google Scholar 

  • Oliver A, Pedersen J, Grant R, Klopfenstein T (2005) Comparative effects of the sorghum bmr-6 and bmr-12 genes: I. Forage sorghum yield and quality. Crop Sci 45:2234–2239

    CAS  Google Scholar 

  • Palmer NA, Sattler SE, Saathoff AJ, Funnell D, Pedersen JF, Sarath G (2008) Genetic background impacts soluble and cell wall-bound aromatics in brown midrib mutants of sorghum. Planta 229:115

    CAS  PubMed  Google Scholar 

  • Pedersen JF, Funnell DL, Toy JJ, Oliver A, Grant R (2006) Registration of twelve grain sorghum genetic stocks near-isogenic for the brown midrib genes bmr-6 and bmr-12. Crop Sci 46:491–493

    Google Scholar 

  • Piquemal J, Chamayou S, Nadaud I, Beckert M, Barrière Y, Mila I, Lapierre C, Rigau J, Puigdomenech P, Jauneau A, Digonnet C, Boudet A-M, Goffner D, Pichon M (2002) Down-regulation of caffeic acid O-methyltransferase in maize revisited using a transgenic approach. Plant Physiol 130:1675–1685

    CAS  PubMed  PubMed Central  Google Scholar 

  • Porter KS, Anxtell JD, Lechtenberg VL, Colenbrander VF (1978) Phenotype, fiber composition, and in vitro dry matter disappearance of chemically induced brown midrib (bmr) mutants of sorghum. Crop Sci. https://doi.org/10.2135/cropsci1978.0011183X001800020002x

    Article  Google Scholar 

  • Pradhan Mitra P, Loqué D (2014) Histochemical staining of Arabidopsis thaliana secondary cell wall elements. J Vis Exp. https://doi.org/10.3791/51381

    Article  PubMed  PubMed Central  Google Scholar 

  • Ragauskas AJ, Beckham GT, Biddy MJ, Chandra R, Chen F, Davis MF, Davison BH, Dixon RA, Gilna P, Keller M (2014) Lignin valorization: improving lignin processing in the biorefinery. Science 344:1246843

    PubMed  Google Scholar 

  • Ralph J, Lapierre C, Marita JM, Kim H, Lu F, Hatfield RD, Ralph S, Chapple C, Franke R, Hemm MR, Van Doorsselaere J, Sederoff RR, O’Malley DM, Scott JT, Mackay JJ, Yahiaoui N, Boudet A-M, Pean M, Pilate G, Jouanin L, Boerjan W (2001) Elucidation of new structures in lignins of CAD- and COMT-deficient plants by NMR. Phytochemistry 57:993–1003

    CAS  PubMed  Google Scholar 

  • Ralph J, Lundquist K, Brunow G, Lu F, Kim H, Schatz PF, Marita JM, Hatfield RD, Ralph SA, Christensen JH (2004) Lignins: natural polymers from oxidative coupling of 4-hydroxyphenyl-propanoids. Phytochem Rev 3:29–60

    CAS  Google Scholar 

  • Rastogi S, Dwivedi UN (2006) Down-regulation of lignin biosynthesis in transgenic Leucaena leucocephala harboring O-methyltransferase gene. Biotechnol Prog 22:609–616

    CAS  PubMed  Google Scholar 

  • Reddy MSS, Chen F, Shadle G, Jackson L, Aljoe H, Dixon RA (2005) Targeted down-regulation of cytochrome P450 enzymes for forage quality improvement in alfalfa (Medicago sativa L.). Proc Natl Acad Sci USA 102:16573–16578

    CAS  PubMed  Google Scholar 

  • Rogers SO, Bendich AJ (1985) Extraction of DNA from milligram amounts of fresh, herbarium and mummified plant tissues. Plant Mol Biol 5:69–76

    CAS  PubMed  Google Scholar 

  • Rooney WL (2004) Sorghum improvement—integrating traditional and new technology to produce improved genotypes. Adv Agron 83:37–109

    Google Scholar 

  • Saballos A, Ejeta G, Sanchez E, Kang CH, Vermerris W (2009) A genomewide analysis of the cinnamyl alcohol dehydrogenase family in sorghum [Sorghum bicolor (L.) Moench] identifies SbCAD2 as the brown midrib6 gene. Genetics 181:783–795

    CAS  PubMed  PubMed Central  Google Scholar 

  • Saballos A, Sattler SE, Sanchez E, Foster TP, Xin Z, Kang C, Pedersen JF, Vermerris W (2012) Brown midrib2 (Bmr2) encodes the major 4-coumarate:coenzyme A ligase involved in lignin biosynthesis in sorghum (Sorghum bicolor (L.) Moench). Plant J 70:818–830

    CAS  PubMed  Google Scholar 

  • Sarath G, Mitchell RB, Sattler SE, Funnell D, Pedersen JF, Graybosch RA, Vogel KP (2008) Opportunities and roadblocks in utilizing forages and small grains for liquid fuels. J Ind Microbiol Biotechnol 35:343–354

    CAS  PubMed  Google Scholar 

  • Sattler SE, Saathoff AJ, Haas EJ, Palmer NA, Funnell-Harris DL, Sarath G, Pedersen JF (2009) A nonsense mutation in a cinnamyl alcohol dehydrogenase gene is responsible for the sorghum brown midrib6 phenotype. Plant Physiol 150:584–595

    CAS  PubMed  PubMed Central  Google Scholar 

  • Sattler SE, Funnell-Harris DL, Pedersen JF (2010) Efficacy of singular and stacked brown midrib 6 and 12 in the modification of lignocellulose and grain chemistry. J Agric Food Chem 58:3611–3616

    CAS  PubMed  Google Scholar 

  • Sattler SE, Palmer NA, Saballos A, Greene AM, Xin Z, Sarath G, Vermerris W, Pedersen JF (2012) Identification and characterization of four missense mutations in brown midrib 12 (Bmr12), the caffeic O-methyltransferase (COMT) of sorghum. Bioenergy Res 5:855–865

    CAS  Google Scholar 

  • Scully ED, Gries T, Sarath G, Palmer NA, Baird L, Serapiglia MJ, Dien BS, Boateng AA, Ge Z, Funnell-Harris DL, Twigg P, Clemente TE, Sattler SE (2016) Overexpression of SbMyb60 impacts phenylpropanoid biosynthesis and alters secondary cell wall composition in Sorghum bicolor. Plant J 85:378–395

    CAS  PubMed  Google Scholar 

  • Sewalt VJ, Ni W, Blount JW, Jung HG, Masoud SA, Howles PA, Lamb C, Dixon RA (1997) Reduced lignin content and altered lignin composition in transgenic tobacco down-regulated in expression of l-phenylalanine ammonia-lyase or cinnamate 4-hydroxylase. Plant Physiol 115:41–50

    CAS  PubMed  PubMed Central  Google Scholar 

  • Stewart JJ, Akiyama T, Chapple C, Ralph J, Mansfield SD (2009) The effects on lignin structure of overexpression of ferulate 5-hydroxylase in hybrid poplar. Plant Physiol 150:621–635

    CAS  PubMed  PubMed Central  Google Scholar 

  • Takeda Y, Koshiba T, Tobimatsu Y, Suzuki S, Murakami S, Yamamura M, Rahman MM, Takano T, Hattori T, Sakamoto M (2017) Regulation of CONIFERALDEHYDE 5-HYDROXYLASE expression to modulate cell wall lignin structure in rice. Planta 246:337–349

    CAS  PubMed  Google Scholar 

  • Tetreault HM, Scully ED, Gries T, Palmer NA, Funnell-Harris DL, Baird L, Seravalli J, Dien BS, Sarath G, Clemente TE, Sattler SE (2018) Overexpression of the Sorghum bicolor SbCCoAOMT alters cell wall associated hydroxycinnamoyl groups. PLoS ONE 13:e0204153

    PubMed  PubMed Central  Google Scholar 

  • Towers GHN, Gibbs RD (1953) Lignin chemistry and the taxonomy of higher plants. Nature 172:25–26

    CAS  PubMed  Google Scholar 

  • Vanholme R, Storme V, Vanholme B, Sundin L, Christensen JH, Goeminne G, Halpin C, Rohde A, Morreel K, Boerjan W (2012) A systems biology view of responses to lignin biosynthesis perturbations in Arabidopsis. Plant Cell. https://doi.org/10.1105/tpc.112.102574

    Article  PubMed  PubMed Central  Google Scholar 

  • Vermerris W, Thompson KJ, Mcintyre LM, Axtell JD (2002) Evidence for an evolutionarily conserved interaction between cell wall biosynthesis and flowering in maize and sorghum. BMC Evol Biol 2:2

    PubMed  PubMed Central  Google Scholar 

  • Vignols F, Rigau J, Torres MA, Capellades M, Puigdomenech P (1995) The brown midrib3 (bm3) mutation in maize occurs in the gene encoding caffeic acid O-methyltransferase. Plant Cell 7:407–416

    CAS  PubMed  PubMed Central  Google Scholar 

  • Vogel KP, Pedersen JF, Masterson SD, Toy JJ (1999) Evaluation of a filter bag system for NDF, ADF, and IVDMD forage analysis. Crop Sci 39:276–279

    Google Scholar 

  • Weng JK, Mo H, Chapple C (2010) Over-expression of F5H in COMT-deficient Arabidopsis leads to enrichment of an unusual lignin and disruption of pollen wall formation. Plant J 64:898–911

    CAS  PubMed  Google Scholar 

  • Wu Z, Wang N, Hisano H, Cao Y, Wu F, Liu W, Bao Y, Wang Z-Y, Fu C (2019) Simultaneous regulation of F5H in COMT-RNAi transgenic switchgrass alters effects of COMT suppression on syringyl lignin biosynthesis. Plant Biotechnol J 17:836–845

    CAS  PubMed  Google Scholar 

  • Yue F, Lu F, Sun R-C, Ralph J (2012) Syntheses of lignin-derived thioacidolysis monomers and their uses as quantitation standards. J Agric Food Chem 60:922–928

    CAS  PubMed  Google Scholar 

  • Yue F, Lu F, Regner M, Sun R, Ralph J (2017) Lignin-derived thioacidolysis dimers: reevaluation, new products, authentication, and quantification. Chemsuschem 10:830–835

    CAS  PubMed  PubMed Central  Google Scholar 

  • Zhao H, Wei J, Jinyu Z, Liu H, Tai W, Song Y (2002) Lignin biosynthesis by suppression of two O-methyl-transferases. Chin Sci Bull 47:1092–1095

    CAS  Google Scholar 

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Acknowledgements

We thank John Toy, Coehn Preble, Samantha Timmons and Sara Finnegan for technical assistance, and Dr. Heather Van Buskirk for critically reviewing the manuscript. We thank the Plant Transformation Core Research Facility at the University of Nebraska for creating the overexpression lines. This research was supported by the United States Department of Agriculture: National Institute of Food and Agriculture AFRI Grant Number 2011-67009-30026 (SES and DLF-H) and additional funding from USDA-ARS, CRIS Projects 3042-21220-033-00-D (SES and DLF-H). The University of Nebraska DNA Sequencing Core receives partial support from the National Institute for General Medical Science (NIGMS) INBRE-P20GM103427-14 and COBRE-1P30GM110768-01 Grants as well as The Fred and Pamela Buffett Cancer Center Support Grant: P30CA036727. This publication’s contents are the sole responsibility of the authors and do not necessarily represent the official views of the NIH or NIGMS. The US Department of Agriculture, Agricultural Research Service, is an equal opportunity/affirmative action employer and all agency services are available without discrimination. Mention of commercial products and organizations in this manuscript is solely to provide specific information. It does not constitute endorsement by USDA-ARS over other products and organizations not mentioned.

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HMT, SES and DLFH designed the research; HMT, TG, NAP, SS and ZG performed the experiments; HMT, TG, NAP, DLFH, GS and SES analyzed and interpreted the data; HMT and SES wrote the first draft of the manuscript, and all authors reviewed and revised the manuscript prior to publication.

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Correspondence to Scott E. Sattler.

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Tetreault, H.M., Gries, T., Palmer, N.A. et al. Overexpression of ferulate 5-hydroxylase increases syringyl units in Sorghum bicolor. Plant Mol Biol 103, 269–285 (2020). https://doi.org/10.1007/s11103-020-00991-3

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