High spatial resolution mass spectrometry imaging reveals the genetically programmed, developmental modification of the distribution of thylakoid membrane lipids among individual cells of maize leaf

Duenas, Maria Emilia; Klein, Adam T.; Alexander, Liza E.; Yandeau-Nelson, Marna D.; Nikolau, Basil J.; Lee, Young Jin

doi:10.1111/tpj.13422

Title: High spatial resolution mass spectrometry imaging reveals the genetically programmed, developmental modification of the distribution of thylakoid membrane lipids among individual cells of maize leaf

Journal Article · Thu Nov 17 00:00:00 EST 2016 · The Plant Journal

DOI:https://doi.org/10.1111/tpj.13422· OSTI ID:1347407

Duenas, Maria Emilia ^[1]; Klein, Adam T. ^[1]; Alexander, Liza E. ^[1]; Yandeau-Nelson, Marna D. ^[2]; Nikolau, Basil J. ^[1]; Lee, Young Jin ^[1]

Ames Lab. and Iowa State Univ., Ames, IA (United States)
Iowa State Univ., Ames, IA (United States)

Summary Metabolism in plants is compartmentalized among different tissues, cells and subcellular organelles. Mass spectrometry imaging ( MSI ) with matrix‐assisted laser desorption ionization ( MALDI ) has recently advanced to allow for the visualization of metabolites at single‐cell resolution. Here we applied 5‐ and 10 μm high spatial resolution MALDI ‐ MSI to the asymmetric Kranz anatomy of Zea mays (maize) leaves to study the differential localization of two major anionic lipids in thylakoid membranes, sulfoquinovosyldiacylglycerols ( SQDG ) and phosphatidylglycerols ( PG ). The quantification and localization of SQDG and PG molecular species, among mesophyll (M) and bundle sheath ( BS ) cells, are compared across the leaf developmental gradient from four maize genotypes (the inbreds B73 and Mo17, and the reciprocal hybrids B73 × Mo17 and Mo17 × B73). SQDG species are uniformly distributed in both photosynthetic cell types, regardless of leaf development or genotype; however, PG shows photosynthetic cell‐specific differential localization depending on the genotype and the fatty acyl chain constituent. Overall, 16:1‐containing PG s primarily contribute to the thylakoid membranes of M cells, whereas BS chloroplasts are mostly composed of 16:0‐containing PG s. Furthermore, PG 32:0 shows genotype‐specific differences in cellular distribution, with preferential localization in BS cells for B73, but more uniform distribution between BS and M cells in Mo17. Maternal inheritance is exhibited within the hybrids, such that the localization of PG 32:0 in B73 × Mo17 is similar to the distribution in the B73 parental inbred, whereas that of Mo17 × B73 resembles the Mo17 parent. This study demonstrates the power of MALDI ‐ MSI to reveal unprecedented insights on metabolic outcomes in multicellular organisms at single‐cell resolution.

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Research Organization:: Ames Laboratory (AMES), Ames, IA (United States)

Sponsoring Organization:: USDOE Office of Science (SC), Basic Energy Sciences (BES)

Grant/Contract Number:: EEC-0813570; IOS-1354799; AC02-07CH11358

OSTI ID:: 1347407

Alternate ID(s):: OSTI ID: 1401250

Report Number(s):: IS-J-9218

Journal Information:: The Plant Journal, Vol. 89, Issue 4; ISSN 0960-7412

Publisher:: Society for Experimental BiologyCopyright Statement

Country of Publication:: United States

Language:: English

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Cited by: 41 works

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59 BASIC BIOLOGICAL SCIENCES
mass spectrometry imaging
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Zea mays L.
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single cell

Title: High spatial resolution mass spectrometry imaging reveals the genetically programmed, developmental modification of the distribution of thylakoid membrane lipids among individual cells of maize leaf

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