Pump–Dump–Probe and Pump–Repump–Probe Ultrafast Spectroscopy Resolves Cross Section of an Early Ground State Intermediate and Stimulated Emission in the Photoreactions of the Pr Ground State of the Cyanobacterial Phytochrome Cph1

Saved in:
Bibliographic Details
Title: Pump–Dump–Probe and Pump–Repump–Probe Ultrafast Spectroscopy Resolves Cross Section of an Early Ground State Intermediate and Stimulated Emission in the Photoreactions of the Pr Ground State of the Cyanobacterial Phytochrome Cph1
Authors: Fitzpatrick, Ann E.1, Lincoln, Craig N.1, van Wilderen, Luuk J. G. W.1, van Thor, Jasper J.1
Source: Journal of Physical Chemistry B. Jan2012, Vol. 116 Issue 3, p1077-1088. 12p.
Subjects: Intermediates (Chemistry), Cross-sectional method, Ground state (Quantum mechanics), Chemical reactions, Cyanobacteria, Phytochromes
Abstract: The primary photoreactions of the red absorbing ground state (Pr) of the cyanobacterial phytochrome Cph1 from SynechocystisPCC 6803 involve C15C16 Z–Ephotoisomerization of its phycocyanobilin chromophore. The first observable product intermediate in pump–probe measurements of the photocycle, “Lumi-R”, is formed with picosecond kinetics and involves excited state decay reactions that have 3 and 14 ps time constants. Here, we have studied the photochemical formation of the Lumi-R intermediate using multipulse picosecond visible spectroscopy. Pump–dump–probe (PDP) and pump–repump–probe (PRP) experiments were carried out by employing two femtosecond visible pulses with 1, 14, and 160 ps delays, together with a broadband dispersive visible probe. The time delays between the two excitation pulses have been selected to allow interaction with the dominant (3 and 14 ps) kinetic phases of Lumi-R formation. The frequency dependence of the PDP and PRP amplitudes was investigated at 620, 640, 660, and 680 nm, covering excited state absorption (λmax= 620 nm), ground state absorption (λmax= 660 nm), and stimulated emission (λmax= 680 nm) cross sections. Experimental double difference transient absorbance signals (ΔΔOD), from the PDP and PRP measurements, required corrections to remove contributions from ground state repumping. The sensitivity of the resulting ΔΔOD signals was systematically investigated for possible connectivity schemes and photochemical parameters. When applying a homogeneous (sequentially decaying) connectivity scheme in both the 3 and 14 ps kinetic phases, evidence for repumping of an intermediate that has an electronic ground state configuration (GSI) is taken from the dump-induced S1 formation with 620, 640, and 660 nm wavelengths and 1 and 14 ps repump delays. Evidence for repumping a GSI is also seen, for the same excitation wavelengths, when imposing a target connectivity scheme proposed in the literature for the 1 ps repump delay. In contrast, using a 680 nm dump pulse, ground state formation is observed for all models examined. The ΔΔOD signals were dominated by stimulated emission, at both 1 and 14 ps delays for the longer wavelength excitation. The GSI, which is revealed by the PRP measurements and not resolved from pump–probe measurements, is found to be directly formed from the excited state of Pr, and its formation is considered using heterogeneous, homogeneous, and target models to globally fit the data. [ABSTRACT FROM AUTHOR]
Copyright of Journal of Physical Chemistry B is the property of American Chemical Society and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
Database: Engineering Source
FullText Text:
  Availability: 0
Header DbId: egs
DbLabel: Engineering Source
An: 85433031
AccessLevel: 6
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Pump–Dump–Probe and Pump–Repump–Probe Ultrafast Spectroscopy Resolves Cross Section of an Early Ground State Intermediate and Stimulated Emission in the Photoreactions of the Pr Ground State of the Cyanobacterial Phytochrome Cph1
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AR" term="%22Fitzpatrick%2C+Ann+E%2E%22">Fitzpatrick, Ann E.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Lincoln%2C+Craig+N%2E%22">Lincoln, Craig N.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22van+Wilderen%2C+Luuk+J%2E+G%2E+W%2E%22">van Wilderen, Luuk J. G. W.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22van+Thor%2C+Jasper+J%2E%22">van Thor, Jasper J.</searchLink><relatesTo>1</relatesTo>
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22Journal+of+Physical+Chemistry+B%22">Journal of Physical Chemistry B</searchLink>. Jan2012, Vol. 116 Issue 3, p1077-1088. 12p.
– Name: Subject
  Label: Subjects
  Group: Su
  Data: <searchLink fieldCode="DE" term="%22Intermediates+%28Chemistry%29%22">Intermediates (Chemistry)</searchLink><br /><searchLink fieldCode="DE" term="%22Cross-sectional+method%22">Cross-sectional method</searchLink><br /><searchLink fieldCode="DE" term="%22Ground+state+%28Quantum+mechanics%29%22">Ground state (Quantum mechanics)</searchLink><br /><searchLink fieldCode="DE" term="%22Chemical+reactions%22">Chemical reactions</searchLink><br /><searchLink fieldCode="DE" term="%22Cyanobacteria%22">Cyanobacteria</searchLink><br /><searchLink fieldCode="DE" term="%22Phytochromes%22">Phytochromes</searchLink>
– Name: Abstract
  Label: Abstract
  Group: Ab
  Data: The primary photoreactions of the red absorbing ground state (Pr) of the cyanobacterial phytochrome Cph1 from SynechocystisPCC 6803 involve C15C16 Z–Ephotoisomerization of its phycocyanobilin chromophore. The first observable product intermediate in pump–probe measurements of the photocycle, “Lumi-R”, is formed with picosecond kinetics and involves excited state decay reactions that have 3 and 14 ps time constants. Here, we have studied the photochemical formation of the Lumi-R intermediate using multipulse picosecond visible spectroscopy. Pump–dump–probe (PDP) and pump–repump–probe (PRP) experiments were carried out by employing two femtosecond visible pulses with 1, 14, and 160 ps delays, together with a broadband dispersive visible probe. The time delays between the two excitation pulses have been selected to allow interaction with the dominant (3 and 14 ps) kinetic phases of Lumi-R formation. The frequency dependence of the PDP and PRP amplitudes was investigated at 620, 640, 660, and 680 nm, covering excited state absorption (λmax= 620 nm), ground state absorption (λmax= 660 nm), and stimulated emission (λmax= 680 nm) cross sections. Experimental double difference transient absorbance signals (ΔΔOD), from the PDP and PRP measurements, required corrections to remove contributions from ground state repumping. The sensitivity of the resulting ΔΔOD signals was systematically investigated for possible connectivity schemes and photochemical parameters. When applying a homogeneous (sequentially decaying) connectivity scheme in both the 3 and 14 ps kinetic phases, evidence for repumping of an intermediate that has an electronic ground state configuration (GSI) is taken from the dump-induced S1 formation with 620, 640, and 660 nm wavelengths and 1 and 14 ps repump delays. Evidence for repumping a GSI is also seen, for the same excitation wavelengths, when imposing a target connectivity scheme proposed in the literature for the 1 ps repump delay. In contrast, using a 680 nm dump pulse, ground state formation is observed for all models examined. The ΔΔOD signals were dominated by stimulated emission, at both 1 and 14 ps delays for the longer wavelength excitation. The GSI, which is revealed by the PRP measurements and not resolved from pump–probe measurements, is found to be directly formed from the excited state of Pr, and its formation is considered using heterogeneous, homogeneous, and target models to globally fit the data. [ABSTRACT FROM AUTHOR]
– Name: AbstractSuppliedCopyright
  Label:
  Group: Ab
  Data: <i>Copyright of Journal of Physical Chemistry B is the property of American Chemical Society and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=egs&AN=85433031
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1021/jp206298n
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        PageCount: 12
        StartPage: 1077
    Subjects:
      – SubjectFull: Intermediates (Chemistry)
        Type: general
      – SubjectFull: Cross-sectional method
        Type: general
      – SubjectFull: Ground state (Quantum mechanics)
        Type: general
      – SubjectFull: Chemical reactions
        Type: general
      – SubjectFull: Cyanobacteria
        Type: general
      – SubjectFull: Phytochromes
        Type: general
    Titles:
      – TitleFull: Pump–Dump–Probe and Pump–Repump–Probe Ultrafast Spectroscopy Resolves Cross Section of an Early Ground State Intermediate and Stimulated Emission in the Photoreactions of the Pr Ground State of the Cyanobacterial Phytochrome Cph1
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Fitzpatrick, Ann E.
      – PersonEntity:
          Name:
            NameFull: Lincoln, Craig N.
      – PersonEntity:
          Name:
            NameFull: van Wilderen, Luuk J. G. W.
      – PersonEntity:
          Name:
            NameFull: van Thor, Jasper J.
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 26
              M: 01
              Text: Jan2012
              Type: published
              Y: 2012
          Identifiers:
            – Type: issn-print
              Value: 15206106
          Numbering:
            – Type: volume
              Value: 116
            – Type: issue
              Value: 3
          Titles:
            – TitleFull: Journal of Physical Chemistry B
              Type: main
ResultId 1