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Isolation and classification of chlorophyll-deficient xantha mutants of Arabidopsis thaliana

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Abstract

Mutant lines of Arabidopsis thaliana that are either blocked at various steps of the biosynthetic pathway of chlorophyll (Chl) or that are disturbed in one of the subsequent steps leading to the assembly of an active photosynthetic membrane were isolated by screening for Chl-deficient xantha (xan) mutants. Only mutants that segregated in a 3∶1 ratio, that contained the same carotenoid spectrum as etiolated wild-type seedlings and less than 2% of the Chl of wild-type control seedlings, and whose Chl content was not affected by the addition of sucrose to the growth medium were selected for a more detailed analysis. As a final test for the classification of the selected mutants, light-grown xan mutants were vacuum-infiltrated and incubated with the common precursor of tetrapyrroles, δ-aminolevulinic acid (ALA), in the dark. Two major groups of mutants could be distinguished. Some of the mutants were blocked at various steps of the Chl pathway between ALA and protochlorophyllide (Pchlide) and did not accumulate the latter in the dark. The other mutants accumulated Pchlide in the dark regardless of whether exogenous ALA was added. This latter group could be subdivided into mutants with a biochemical lesion in a recently discovered second light-dependent Pchlide reduction step that occurs in green plants and mutants that have blocks in the assembly of Chl protein complexes. In the present work a total of seven different loci could be defined genetically in Arabidopsis that affect the synthesis of Chl and its integration into the growing photosynthetic membrane.

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Abbreviations

ALA:

δ-aminolevulinic acid

Chl:

chlorophyll

Chlide:

chlorophyllide

Pchlide:

protochlorophyllide

POR:

NADPH-Protochlorophyllide oxidoreductase

xan :

xantha

References

  • Anderson IC, Robertson DS (1960) Role of carotenoids in protecting chloropyll from photodestruction. Plant Physiol 35: 531–534

    Google Scholar 

  • Apel K, Santel H-J, Redlinger TE, Falk H (1980) The protochlorophyllide holochrome of barley (Hordeum vulgare L.): Isolation and characterization of the NADPH-protochlorophyllide oxidoreductase. Eur J Biochem 111: 251–258

    Google Scholar 

  • Armstrong GA, Runge S, Frick G, Sperling U, Apel K (1995) Identification of NADPH-protochlorophyllide oxidoreductases A and B: a branched pathway for light-dependent chlorophyll biosynthesis in Arabidopsis thaliana. Plant Physiol in press

  • Bachmann MD, Robertson DS, Bowen CC, Anderson LC (1973) Chloroplast utrastructure in pigment-deficient mutants of Zea mays und reduced light. J Ultrastruct Res 45: 384–406

    Google Scholar 

  • Beale SI, Weinstein JD (1990) Tetrapyrrole metabolism in photosynthetic organisms. In: Dailey H (ed.) Biosynthesis of heme and chlorophyll. McGraw-Hill, New York, pp 287–391

    Google Scholar 

  • Becerril M, Duke SO (1989) Protoporphyrin IX content correlates with activity of photobleaching herbicides. Plant Physiol 90: 1175–1181

    Google Scholar 

  • Benli M, Schulz R, Apel K (1991) Effect of light on the NADPH-protochlorophyllide oxidoreductase of Arabidopsis thaliana. Plant Mol Biol 16: 615–625

    Google Scholar 

  • Boardman NK, Anderson JM, Goodchild DJ (1978) Chlorophyllprotein complexes and structure of mature and developing chloroplasts. Curr Top Bioenerg 8: 35–109

    Google Scholar 

  • Bogorad L (1967) Biosynthesis and morphogenesis in plastids. In: Goodwin TW (ed.) Biochemistry of chloroplasts. Academic Press, New York, pp 615–631

    Google Scholar 

  • Castelfranco PA, Beale SI (1983) Chlorophyll biosynthesis: recent advances and areas of current interest. Annu Rev Plant Physiol 34: 241–278

    Google Scholar 

  • Estelle MA, Somerville C (1987) Auxin-resistant mutants of Arabidopsis thaliana with an altered morphology. Mol Gen Genet 206: 200–206

    Google Scholar 

  • Forreiter C, van Cleve B, Schmidt A, Apel K (1990) Evidence for a general light-dependent negative control of NADPH-protochlorophyllide oxidoreductase in angiosperms. Planta 183: 126–132

    Google Scholar 

  • Gough S (1972) Defective synthesis of porphyrins in barley plastids caused by mutations in nuclear genes. Biochim Biophys Acta 286: 36–54

    Google Scholar 

  • Granick S (1959) Magnesium porphyrins formed by barley seedlings treated with δ-aminolevulinic acid. Plant Physiol 34: XVIII

    Google Scholar 

  • Griffiths WT (1978) Reconstitution of chlorophyllide formation by isolated etioplast membranes. Biochem J 174: 681–692

    Google Scholar 

  • Harpster M, Apel K (1985) Light-dependent regulation of gene expression during plastid development in higher plants. Physiol Plant 64: 147–152

    Google Scholar 

  • Holtorf H, Reinbothe S, Reinbothe C, Bereza B, Apel K (1995) Two routes of chlorophyllide synthesis that are differentially regulated by light in barley (Hordeum vulgare L.). Proc Natl Acad Sci USA 92: 3254–3258

    Google Scholar 

  • Jacobs JM, Jacobs NJ (1993) Porphyrin accumulation and export by isolated barley (Hordeum vulgare) plastids. Plant Physiol 101: 1181–1187

    Google Scholar 

  • Klein S, Katz E, Neeman E (1977) Induction of δ-aminolevulinic acid formation in etiolated maize leaves controlled by two light systems. Plant Physiol 60: 335–338

    Google Scholar 

  • Lehnen LP, Sherman TD, Becerril JM, Duke SO (1990) Tissue and cellular localization of acifluorfen-induced porphyrins in cucumber cotyledons. Pestic Biochem Physiol 37: 239–248

    Google Scholar 

  • Li SL, Rédei GP (1969) Estimation of mutation rate in autogamous diploids. Radiat Bot 9: 125–131

    Google Scholar 

  • Mascia P (1978) An analysis of precursors accumulated by several chlorophyll biosynthetic mutants of maize. Mol Gen Genet 161: 237–244

    Google Scholar 

  • Matringe M, Camadro J-M, Labbe P, Scalla R (1989) Protoporphyrinogen oxidase as a molecular target for diphenyl ether herbicides. Biochem J 260: 231–235

    Google Scholar 

  • Müller AJ (1963) Embryotest zum Nachweis rezessiver Letalfaktoren bei Arabidopsis thaliana. Biol Zentralbl 82: 132–163

    Google Scholar 

  • Murashige T, Skoog F (1962) A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol Plant 15: 473–497

    CAS  Google Scholar 

  • Röbbelen G (1956) Ueber die Protochlorophyllidreduktion in einer Mutante von Arabidopsis thaliana (L.) Heynh. Planta 47: 532–546

    Google Scholar 

  • Runge S (1994) Molekularbiologische und genetische Charakterisierung der NADPH-Protochlorophyllid Oxidoreduktase während der lichtinduzierten Ergrünung von Arabidopsis thaliana. Ph.D. thesis, ETH Zurich, Switzerland

    Google Scholar 

  • Schulz R, Steinmüller K, Klaas M, Forreiter C, Rasmussen S, Hiller C, Apel K (1989) Nucleotide sequence of a cDNA coding for the NADPH-protochlorophyllide oxidoreductase (PCR) of barley (Hordeum vulgare L.) and its expression in Escherichia coli. Mol Gen Genet 217: 355–361

    Article  Google Scholar 

  • Siffel P, Lebedev NN, Krasnovskii AA (1987) Detection of shortwavelength chlorophyll a emission in green leaves. Photosynthetica 21: 23–28

    Google Scholar 

  • Smith AG (1988) Subcellular localization of two porphyrin-synthesis enzymes in Pisum sativum (pea) and Arum (cuckoo-pint) species. Biochem J 249: 423–428

    Google Scholar 

  • Smith AG, Marsh O, Elder G (1993) Investigation of the subcellular location of the tetrapyrrole-biosynthesis enzyme coproporphyrinogen oxidase in higher plants. Biochem J 292: 503–508

    Google Scholar 

  • Somerville CR (1986) Analysis of photosynthesis with mutants of higher plants and algae. Annu Rev Plant Physiol 37: 467–507

    Google Scholar 

  • Thompson WF, White MJ (1991) Physiological and molecular studies of light-regulated nuclear genes in higher plants. Annu Rev Plant Physiol Plant Mol Biol 42: 423–466

    Google Scholar 

  • Vernon LP, Seely GR (1966) The chlorophylls. Academic Press, New York

    Google Scholar 

  • von Wettstein D, Henningsen KW, Boynton JE, Kannangara GC, Nielsen OF (1971) The genetic control of chloroplast development in barley. In: Boardman NK, Linnane AW, Smillie RM (eds) Autonomy and biogenesis of mitochondria and chloroplasts. North-Holland, Amsterdam, pp 205–223

    Google Scholar 

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This study was initiated while one of the authors (K.A.) was on sabbatical leave in the laboratory of Dr. C. Somerville (MSU, East Lansing, Mich., USA). We are extremely grateful to Dr. Somerville and his coworkers for advice and support during this time. This research was supported by the Deutsche Forschungsgemeinschaft and the Schweizerischer Nationalfonds.

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Runge, S., van Cleve, B., Lebedev, N. et al. Isolation and classification of chlorophyll-deficient xantha mutants of Arabidopsis thaliana . Planta 197, 490–500 (1995). https://doi.org/10.1007/BF00196671

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  • DOI: https://doi.org/10.1007/BF00196671

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