In vivo or whole-cell solid-state NMR is an emerging field which faces tremendous challenges. In most cases, cell biochemistry does not allow the labelling of specific molecules and an in vivo study is thus hindered by the inherent difficulty of identifying, among a formidable number of resonances, those arising from a given molecule. In this work we examined the possibility of studying, by solid-state NMR, the model organism Chlamydomonas reinhardtii fully and non-specifically 13C labelled. The extension of NMR-based dynamic filtering from one-dimensional to two-dimensional experiments enabled an enhanced selectivity which facilitated the assignment of cell constituents. The number of resonances detected with these robust and broadly applicable experiments appears to be surprisingly sparse. Various constituents, notably galactolipids abundant in organelle membranes, carbohydrates from the cell wall, and starch from storage grains could be unambiguously assigned. Moreover, the dominant crystal form of starch could be determined in situ. This work illustrates the feasibility and caveats of using solid-state NMR to study intact non-specifically 13C labelled micro-organisms.
Dynamics of Lysine as a Heme Axial Ligand: NMR Analysisof the Chlamydomonas reinhardtii Hemoglobin THB1
Dynamics of Lysine as a Heme Axial Ligand: NMR Analysisof the Chlamydomonas reinhardtii Hemoglobin THB1
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/bichaw/0/bichaw.ahead-of-print/acs.biochem.6b00926/20170118/images/medium/bi-2016-00926m_0015.gif
Biochemistry
DOI: 10.1021/acs.biochem.6b00926
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01-19-2017 08:56 AM
[NMR paper] The dynamics of lysine as a heme axial ligand: NMR analysis of the Chlamydomonas reinhardtii hemoglobin THB1.
The dynamics of lysine as a heme axial ligand: NMR analysis of the Chlamydomonas reinhardtii hemoglobin THB1.
Related Articles The dynamics of lysine as a heme axial ligand: NMR analysis of the Chlamydomonas reinhardtii hemoglobin THB1.
Biochemistry. 2016 Dec 29;:
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Abstract
Nitrate metabolism in Chlamydomonas reinhardtii involves THB1, a monomeric hemoglobin thought to function as a nitric oxide dioxygenase (NOD). NOD activity requires dioxygen and nitric oxide binding followed by...
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12-30-2016 04:53 PM
[NMR paper] In-Cell Solid-State NMR: An Emerging Technique for the Study of Biological Membranes.
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Abstract
Biological molecular processes are often studied in model systems, which simplifies their inherent complexity but may...
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12-28-2015 12:26 AM
[NMR paper] A 2H solid-state NMR study of lipid clustering by cationic antimicrobial and cell-penetrating peptides in model bacterial membranes.
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Abstract
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07-12-2014 04:28 AM
[NMR paper] (1)H, (13)C and (15)N NMR assignments of Mg (2+) bound form of UV inducible transcript protein (UVI31+) from Chlamydomonas reinhardtii.
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Abstract
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[NMR paper] (1)H, (13)C and (15)N NMR assignments of a mutant of UV inducible transcript (S55A-UVI31+) from Chlamydomonas reinhardtii.
(1)H, (13)C and (15)N NMR assignments of a mutant of UV inducible transcript (S55A-UVI31+) from Chlamydomonas reinhardtii.
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Biomol NMR Assign. 2013 Aug 27;
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Abstract
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08-28-2013 11:43 AM
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02-02-2011 02:40 AM
[NMR paper] The single mutation Trp35-->Ala in the 35-40 redox site of Chlamydomonas reinhardtii
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