Fourier transform visible and infrared difference spectroscopy for the study of P700 in photosystem I from Fischerella thermalis PCC 7521 cells grown under white light and far-red light: Evidence that the A-1 cofactor is chlorophyll f
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Hastings, Gary
[1
]
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Makita, Hiroki
[1
]
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Agarwala, Neva
[1
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Rohani, Leyla
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Georgia State Univ, Dept Phys & Astron, Atlanta, GA 30303 USAGeorgia State Univ, Dept Phys & Astron, Atlanta, GA 30303 USA
Rohani, Leyla
[1
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Shen, Gaozhong
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Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USAGeorgia State Univ, Dept Phys & Astron, Atlanta, GA 30303 USA
Shen, Gaozhong
[2
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Bryant, Donald A.
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Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
Montana State Univ, Dept Chem & Biochem, Bozeman, MT 59717 USAGeorgia State Univ, Dept Phys & Astron, Atlanta, GA 30303 USA
Bryant, Donald A.
[2
,3
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[1] Georgia State Univ, Dept Phys & Astron, Atlanta, GA 30303 USA
[2] Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
[3] Montana State Univ, Dept Chem & Biochem, Bozeman, MT 59717 USA
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BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
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2019年
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1860卷
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06期
(P700(+)-P700) Fourier transform visible and infrared difference spectra (DS) have been obtained using photosystem I (PSI) complexes isolated from cells of Fischerella thermalis PCC 7521 grown under white light (WL) or far-red light (FRL). PSI from cells grown under FRL (FRL-PSI) contain similar to 8 chlorophyll f (Chl f) molecules (Shen et al., Photosynth Res. Jan. 2019). Both the visible and infrared DS indicate that neither the P-A or P-B pigments of P700 are Chl f molecules, but do support the conclusion that at least one of the A-1 cofactors is a Chl f molecule. The FTIR DS indicate that the hydrogen bond to the 13(1)-keto C=O group of the PA pigment of P700 is weakened in FRL-PSI, as might be expected given that the proteins that bind the P700 pigments are substantially different in FRL-PSI (Gan et al., Science 345, 1312-1317, 2014). The FTIR DS obtained using FRL-PSI display a band at 1664 cm(-1) that is assigned (based on density functional theory calculations) to the 2(1)-formyl C=O group of Chl f, that upshifts 5 cm(-1) upon P700(+) formation. This is much less than expected for a cation-induced upshift, indicating that the Chl f molecule is not one of the pigments of P700. In WL-PSI the A(-1) cofactor is a Chl a molecule with 13(1)-keto and 13(3)-methylester C=O mode vibrations at 1696 and 1750 cm(-1) respectively. In FRL-PSI the A(-1) cofactor is a Chl f molecule with 13(1)-keto and 13(3)-methylester C=O mode vibrations at 1702 and 1754 cm(-1), respectively.
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Russian Acad Sci, NN Semenov Fed Res Ctr Chem Phys, Kosygina St 4, Moscow 117977, Russia
Moscow MV Lomonosov State Univ, AN Belozersky Inst Phys Chem Biol, Leninskie Gory 1,Bldg 40, Moscow 119992, RussiaRussian Acad Sci, NN Semenov Fed Res Ctr Chem Phys, Kosygina St 4, Moscow 117977, Russia
Cherepanov, Dmitry A.
Shelaev, Ivan, V
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Russian Acad Sci, NN Semenov Fed Res Ctr Chem Phys, Kosygina St 4, Moscow 117977, RussiaRussian Acad Sci, NN Semenov Fed Res Ctr Chem Phys, Kosygina St 4, Moscow 117977, Russia
Shelaev, Ivan, V
Gostev, Fedor E.
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Russian Acad Sci, NN Semenov Fed Res Ctr Chem Phys, Kosygina St 4, Moscow 117977, RussiaRussian Acad Sci, NN Semenov Fed Res Ctr Chem Phys, Kosygina St 4, Moscow 117977, Russia
Gostev, Fedor E.
Aybush, Arseniy, V
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Russian Acad Sci, NN Semenov Fed Res Ctr Chem Phys, Kosygina St 4, Moscow 117977, RussiaRussian Acad Sci, NN Semenov Fed Res Ctr Chem Phys, Kosygina St 4, Moscow 117977, Russia
Aybush, Arseniy, V
Mamedov, Mahir D.
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Moscow MV Lomonosov State Univ, AN Belozersky Inst Phys Chem Biol, Leninskie Gory 1,Bldg 40, Moscow 119992, RussiaRussian Acad Sci, NN Semenov Fed Res Ctr Chem Phys, Kosygina St 4, Moscow 117977, Russia
Mamedov, Mahir D.
Shen, Gaozhong
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Penn State Univ, Dept Biochem & Mol Biol, 108 Althouse Lab, University Pk, PA 16802 USARussian Acad Sci, NN Semenov Fed Res Ctr Chem Phys, Kosygina St 4, Moscow 117977, Russia
Shen, Gaozhong
Nadtochenko, Victor A.
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Russian Acad Sci, NN Semenov Fed Res Ctr Chem Phys, Kosygina St 4, Moscow 117977, RussiaRussian Acad Sci, NN Semenov Fed Res Ctr Chem Phys, Kosygina St 4, Moscow 117977, Russia
Nadtochenko, Victor A.
Bryant, Donald A.
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Penn State Univ, Dept Biochem & Mol Biol, 108 Althouse Lab, University Pk, PA 16802 USA
Montana State Univ, Dept Chem & Biochem, 103 Chem & Biochem Bldg,POB 173400, Bozeman, MT 59717 USARussian Acad Sci, NN Semenov Fed Res Ctr Chem Phys, Kosygina St 4, Moscow 117977, Russia
Bryant, Donald A.
Semenov, Alexey Yu
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Russian Acad Sci, NN Semenov Fed Res Ctr Chem Phys, Kosygina St 4, Moscow 117977, Russia
Moscow MV Lomonosov State Univ, AN Belozersky Inst Phys Chem Biol, Leninskie Gory 1,Bldg 40, Moscow 119992, RussiaRussian Acad Sci, NN Semenov Fed Res Ctr Chem Phys, Kosygina St 4, Moscow 117977, Russia
Semenov, Alexey Yu
Golbeck, John H.
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Penn State Univ, Dept Biochem & Mol Biol, 108 Althouse Lab, University Pk, PA 16802 USA
Penn State Univ, Dept Chem, 104 Chem Bldg, University Pk, PA 16802 USARussian Acad Sci, NN Semenov Fed Res Ctr Chem Phys, Kosygina St 4, Moscow 117977, Russia
Golbeck, John H.
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