Skip to main content
Log in

Aggregation of 8,12-diethyl farnesyl bacteriochlorophyll c at low temperature

  • Regular Paper
  • Published:
Photosynthesis Research Aims and scope Submit manuscript

Abstract

The effect of temperature on the aggregation of 3lR-8,12-diethyl farnesyl bacteriochlorophyll c in a mixture of n-pentane and methylcyclohexane (1/1, v/v) was studied by means of absorption, circular dichroism and fluorescence spectroscopy. At room temperature essentially only two aggregate species, absorbing at 702 nm (A-702) and 719 nm (A-719), were present. Upon cooling to 219 K, A-702 was quantitatively converted to A-719. Further lowering of the temperature led to the stepwise formation of larger aggregates by the conversion of A-719 to aggregate species absorbing at 743 nm (A-743) and 755 nm (A-755). All absorption changes were reversible. A-719 was highly fluorescent (maximum at 192 K: 744 nm), while A-743 and especially A-755 were weakly fluorescent. Below 130 K the mixture solidified, and no major changes in the absorption spectrum were observed upon further cooling. At 45 K, however, a relatively strong emission at 775 nm was observed. Below 200 K, the absorption, fluorescence and circular dichroism spectra resembled that of the chlorosome. These results open up the possibility to study higher aggregates of BChl c as models for the chlorosome by various methods at low temperature, thus avoiding interference by thermal processes.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

A-680, A-702, A-719, A-743 and A-755-:

BChl c aggregates absorbing at the wavelengths indicated

BChl-:

bacteriochlorophyll

R[E,E] BChl c F-:

the 31 R isomer of 8,12-diethyl BChl c esterified with farnesol (F), analogously

M-:

methyl

Pr-:

propyl

S-:

stearol (see Smith 1994)

CD-:

circular dichroism

References

  • Alden RG, Lin SH and Blankenship RE (1992) Theory of spectroscopy and energy transfer of oligomeric pigments in chlorosome antennas of green photosynthetic bacteria. J Lumin 51: 51–66

    Google Scholar 

  • Blankenship RE, Brune DC, Freeman JM, King GH, Mc Manus JD, Nozawa T, Trost T and Wittmershaus BP (1988) Energy trapping and electron transfer in Chloroflexus aurantiacus. In: Olson JM, Ormerod JG, Amesz J, Stackebrandt E and Truper HG (eds) Green Photosynthetic Bacteria, pp 57–68. Plenum Press, New York

    Google Scholar 

  • Borrego CM and Garcia-Gill LJ (1994) Separation of bacteriochlorophyll homologues from green photosynthetic sulfur bacteria by reversed-phase HPLC. Photosynth Res 41: 157–163

    Google Scholar 

  • Brune D, Nozawa T and Blankenship R (1987) Antenna organization in green photosynthetic bacteria 1. Oligomeric bacteriochlorophyll c as a model for the 740 nm absorbing bacteriochlorophyll c in Chloroflexus aurantiacus. Biochemistry 26: 8644–8652

    Google Scholar 

  • Brune DC, Gerola PD and Olson JM (1990) Circular dichroism of green bacterial chlorosomes. Photosynth Res 24: 253–263

    Google Scholar 

  • Bystrova MI, Mal'gosheva IN and Krasnovskii AA (1979) Study of molecular mechanism of self-assembly of aggregated forms of bacteriochlorophyll c. Mol Biol USSR 13: 582–594

    Google Scholar 

  • Caple MB, Chow H-C and Strouse CE (1978) Photosynthetic pigments of green sulfur bacteria. The esterifying alcohols of bacteriochlorophylls c from Chlorobium limicola. J Biol Chem 253: 6730–6737

    Google Scholar 

  • Causgrove TP, Cheng P, Brune DC and Blankenship RE (1993) Optical spectroscopy of a highly fluorescent aggregate of bacteriochlorophyll c. J Phys Chem 97: 5519–5524

    Google Scholar 

  • Chiefari J, Griebenow K, Fages F, Griebenow N, Balaban TS, Holzwarth AR and Schaffner K (1995) Models for the pigment organization in the chlorosomes of photosynthetic bacteria: Diastereoselective control of in-vitro bacteriochlorophyll c S aggregation. J Phys Chem 99: 1357–1365

    Google Scholar 

  • Fong FK and Koester VJ (1976) In vitro preparation and characterization of a 700 nm absorbing chlorophyll-water adduct according to the proposed primary molecular unit in photosynthesis. Biochim Biophys Acta 423: 52–64

    Google Scholar 

  • Francke C, Otte SCM, van der Heiden JC and Amesz J (1994) Spurious circular dichroism signals with intact cells of heliobacteria. Biochim Biophys Acta 1186: 75–80

    Google Scholar 

  • Gerola PD and Olson JM (1986) A new bacteriochlorophyll a-protein complex associated with chlorosomes of green sulfur bacteria. Biochim Biophys Acta 848: 69–76

    Google Scholar 

  • Hildebrandt P, Griebenow K, Holzwarth AR and Schaffner K (1991) Resonance Raman spectroscopic evidence for the identity of the bacteriochlorophyll c organization in protein-free and protein-containing chlorosomes from Chloroflexus aurantiacus. Z Naturforsch 46c: 228–232

    Google Scholar 

  • Hirota M, Moriyama T, Shimada K, Miller M, Olson JM and Matsuura K (1992) High degree of organization of bacteriochlorophyll c in chlorosome-like aggregates spontaneously assembled in aqueous solution. Biochim Biophys Acta 1099: 271–274

    Google Scholar 

  • Hoff AJ and Amesz J (1991) Visible absorption spectroscopy of chlorophylls. In: Scheer H (ed) Chlorophylls, pp 723–738. CRC Press, Boca Raton

    Google Scholar 

  • Holzwarth AR, Griebenow K and Schaffner K (1992) Chlorosomes, photosynthetic antennae with novel self-organized pigment structures. J Photochem Photobiol A 65: 61–71

    Google Scholar 

  • Matsuura K and Olson JM (1990) Reversible conversion of aggregated bacteriochlorophyll c to the monomeric form by 1-hexanol in chlorosomes from Chlorobium and Chloroflexus. Biochim Biophys Acta 1019: 233–238

    Google Scholar 

  • Miller M, Gillbro T and Olson JM (1993) Aqueous aggregates of bacteriochlorophyll c as a model for pigment organization in chlorosomes. Photochem Photobiol 57: 98–102

    Google Scholar 

  • Nozawa T, Ohtomo K, Suzuki M, Morishita Y and Madigan MT (1991) Structures of bacteriochlorophyll c's in chlorosomes from a new thermophilic bacterium Chlorobium tepidum. Chem Lett: 1763–1766

  • Nozawa T, Ohtomo K, Suzuki M, Nakagawa H, Shikima Y, Konami H and Zeng-Yu Wang (1994) Structures of chlorosomes and aggregated BChl c in Chlorobium tepidum from solid state high resolution CP/MAS 13C NMR. Photosynth Res 41: 211–223

    Google Scholar 

  • Olson JM (1980) Chlorophyll organization in green photosynthetic bacteria. Biochim Biophys Acta 594: 33–51

    Google Scholar 

  • Olson JM and Cox RP (1991) Monomers, dimers and tetramers of 4-n propyl-5-ethyl farnesyl bacteriochlorophyll c in dichloromethane and carbon tetrachloride. Photosynth Res 30: 35–43

    Google Scholar 

  • Olson JM and Pedersen JP (1990) Bacteriochlorophyll c monomers, dimers, and higher aggregates in dichloromethane, chloroform, and carbon tetrachloride. Photosynth Res 25: 25–37

    Google Scholar 

  • Otte SCM, van der Heiden JC, Pfennig N and Amesz J (1991) A comparative study of the optical characteristics of intact cells of photosynthetic green sulfur bacteria containing bacteriochlorophyll c, d or e. Photosynth Res 28: 159–169

    Google Scholar 

  • Otte SCM, van de Meent EJ, van Veelen PA, Pundsness AS and Amesz J (1993) Identification of the major chlorosomal bacteriochlorophylls of the green sulfur bacteria Chlorobium vibrioforme and Chlorobium phaeovibrioides; their function in lateral energy transfer. Photosynth Res 35: 159–169

    Google Scholar 

  • Smith KM (1994) Nomenclature of the bacteriochlorophylls c, d and e. Photosynth Res 41: 23–26

    Google Scholar 

  • Smith KM, Kehres LA and Fajer J (1983a) Aggregation of the bacteriochlorophylls c, d and e. Models for the antenna chlorophylls of green and brown photosynthetic bacteria. J Am Chem Soc 105: 1387–1389

    Google Scholar 

  • Smith KM, Craig CW, Kehres LA and Pfennig N (1983b) Reversedphase high-performance liquid chromatography and structural assignments of the bacteriochlorophylls c. J Chromatography 281: 209–223.

    Google Scholar 

  • Uehara K and Olson JM (1992) Aggregation of bacteriochlorophyll c homologs to dimers, tetramers and polymers in water saturated carbon tetrachloride. Photosynth Res 33: 251–257

    Google Scholar 

  • Uehara K, Ozaki Y, Okada K and Olson JM (1991) FT-IR studies on the aggregation of bacteriochlorophyll c from Chlorobium limicola. jtChem Lett 909–912

  • van Dorssen RJ, Gerola PD, Olson JM andAmesz J (1986) Optical and structural properties of chlorosomes of the photosynthetic green sulfur bacterium Chlorobium limicola. Biochim Biophys Acta 848: 77–82

    Google Scholar 

  • van Noort PI, Francke C, Schoumans N, Otte SCM, Aartsma TJ and Amesz J (1994) Chlorosomes of green sulfur bacteria: Pigment composition and energy transfer. Photosynth Res 41: 193–203.

    Google Scholar 

  • Worchester DL, Michalski TJ and Katz JJ (1986) Small-angle neutron scattering studies of chlorophyll micelles: Models for bacterial antenna chlorophyll. Proc Natl Acad Sci USA 83: 3791–3795

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Dudkowiak, A., Francke, C. & Amesz, J. Aggregation of 8,12-diethyl farnesyl bacteriochlorophyll c at low temperature. Photosynth Res 46, 427–433 (1995). https://doi.org/10.1007/BF00032297

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00032297

Key words

Navigation