24 research outputs found
Phosphorylation of bacterial-type phosphoenolpyruvate carboxylase at Ser425 provides a further tier of enzyme control in developing castor oil seeds
PEPC [PEP (phosphoenolpyruvate) carboxylase] is a tightly controlled anaplerotic enzyme situated at a pivotal branch point of plant carbohydrate metabolism. Two distinct oligomeric PEPC classes were discovered in developing COS (castor oil seeds). Class-1 PEPC is a typical homotetramer of 107 kDa PTPC (plant-type PEPC) subunits, whereas the novel 910-kDa Class-2 PEPC hetero-octamer arises from a tight interaction between Class-1 PEPC and 118 kDa BTPC (bacterial-type PEPC) subunits. Mass spectrometric analysis of immunopurified COS BTPC indicated that it is subject to in vivo proline-directed phosphorylation at Ser425. We show that immunoblots probed with phosphorylation site-specific antibodies demonstrated that Ser425 phosphorylation is promoted during COS development, becoming maximal at stage IX (maturation phase) or in response to depodding. Kinetic analyses of a recombinant, chimaeric Class-2 PEPC containing phosphomimetic BTPC mutant subunits (S425D) indicated that Ser425 phosphorylation results in significant BTPC inhibition by: (i) increasing its Km(PEP) 3-fold, (ii) reducing its I50 (L-malate and L-aspartate) values by 4.5- and 2.5-fold respectively, while (iii) decreasing its activity within the physiological pH range. The developmental pattern and kinetic influence of Ser425 BTPC phosphorylation is very distinct from the in vivo phosphorylation/activation of COS Class-1 PEPC's PTPC subunits at Ser11. Collectively, the results establish that BTPC's phospho-Ser425 content depends upon COS developmental and physiological status and that Ser425 phosphorylation attenuates the catalytic activity of BTPC subunits within a Class-2 PEPC complex. To the best of our knowledge, this study provides the first evidence for protein phosphorylation as a mechanism for the in vivo control of vascular plant BTPC activity
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An integrated omics analysis reveals molecular mechanisms that are associated with differences in seed oil content between Glycine max and Brassica napus
Abstract
Background: Rapeseed (Brassica napus L.) and soybean (Glycine max L.) seeds are rich in both protein and oil, which
are major sources of biofuels and nutrition. Although the difference in seed oil content between soybean (~ 20%) and
rapeseed (~ 40%) exists, little is known about its underlying molecular mechanism.
Results: An integrated omics analysis was performed in soybean, rapeseed, Arabidopsis (Arabidopsis thaliana L. Heynh),
and sesame (Sesamum indicum L.), based on Arabidopsis acyl-lipid metabolism- and carbon metabolism-related genes.
As a result, candidate genes and their transcription factors and microRNAs, along with phylogenetic analysis and
co-expression network analysis of the PEPC gene family, were found to be largely associated with the difference
between the two species. First, three soybean genes (Glyma.13G148600, Glyma.13G207900 and Glyma.12G122900)
co-expressed with GmPEPC1 are specifically enriched during seed storage protein accumulation stages, while the
expression of BnPEPC1 is putatively inhibited by bna-miR169, and two genes BnSTKA and BnCKII are co-expressed
with BnPEPC1 and are specifically associated with plant circadian rhythm, which are related to seed oil biosynthesis. Then,
in de novo fatty acid synthesis there are rapeseed-specific genes encoding subunits β-CT (BnaC05g37990D) and BCCP1
(BnaA03g06000D) of heterogeneous ACCase, which could interfere with synthesis rate, and β-CT is positively regulated by
four transcription factors (BnaA01g37250D, BnaA02g26190D, BnaC01g01040D and BnaC07g21470D). In triglyceride synthesis,
GmLPAAT2 is putatively inhibited by three miRNAs (gma-miR171, gma-miR1516 and gma-miR5775). Finally, in rapeseed
there was evidence for the expansion of gene families, CALO, OBO and STERO, related to lipid storage, and
the contraction of gene families, LOX, LAH and HSI2, related to oil degradation.
Conclusions: The molecular mechanisms associated with differences in seed oil content provide the basis for
future breeding efforts to improve seed oil content
In Vivo Regulatory Phosphorylation of Novel Phosphoenolpyruvate Carboxylase Isoforms in Endosperm of Developing Castor Oil Seeds
Our previous research characterized two phosphoenolpyruvate (PEP) carboxylase (PEPC) isoforms (PEPC1 and PEPC2) from developing castor oil seeds (COS). The association of a shared 107-kD subunit (p107) with an immunologically unrelated bacterial PEPC-type 64-kD polypeptide (p64) leads to marked physical and kinetic differences between the PEPC1 p107 homotetramer and PEPC2 p107/p64 heterooctamer. Here, we describe the production of antiphosphorylation site-specific antibodies to the conserved p107 N-terminal serine-6 phosphorylation site. Immunoblotting established that the serine-6 of p107 is phosphorylated in COS PEPC1 and PEPC2. This phosphorylation was reversed in vitro following incubation of clarified COS extracts or purified PEPC1 or PEPC2 with mammalian protein phosphatase type 2A and is not involved in a potential PEPC1 and PEPC2 interconversion. Similar to other plant PEPCs examined to date, p107 phosphorylation increased PEPC1 activity at pH 7.3 by decreasing its K(m)(PEP) and sensitivity to l-malate inhibition, while enhancing glucose-6-P activation. By contrast, p107 phosphorylation increased PEPC2's K(m)(PEP) and sensitivity to malate, glutamic acid, and aspartic acid inhibition. Phosphorylation of p107 was promoted during COS development (coincident with a >5-fold increase in the I(50) [malate] value for total PEPC activity in desalted extracts) but disappeared during COS desiccation. The p107 of stage VII COS became fully dephosphorylated in planta 48 h following excision of COS pods or following 72 h of dark treatment of intact plants. The in vivo phosphorylation status of p107 appears to be modulated by photosynthate recently translocated from source leaves into developing COS
complex of
Bacterial- and plant-type phosphoenolpyruvate carboxylase polypeptides interact in the hetero-oligomeric Class-2 PEP
pH and carbon supply control the expression of phosphoenolpyruvate carboxylase kinase genes in Arabidopsis thaliana
Phosphoenolpyruvate carboxylase (PEPC) is thought to play many roles in C<sub>3</sub> plants including the provision of biosynthetic precursors and control of pH during N assimilation. Its activity is controlled via phosphorylation catalysed by PEPC kinases, which are encoded by <i>PPCK</i> genes. We examined <i>PPCK</i> expression in response to changes in the supply of N or C, and to changes in intracellular pH, using cultured Arabidopsis cells and seedlings. The results show that expression of both <i>PPCK1</i> and <i>PPCK2</i> is increased by C availability, but does not respond to N availability. Expression of the two <i>PPCK</i> genes and the phosphorylation state of PEPC are increased in response to increasing intracellular pH. Elevated pH also reduces the repression of <i>PPCK</i> gene expression by P<sub>i</sub>. Expression of phosphoenolpyruvate carboxykinase (PEPCK), which catalyses the decarboxylation of oxaloacetate, is decreased in response to increasing intracellular pH. pH homeostasis may be mediated at least partly by reciprocal changes in the expression of <i>PPCK</i> genes and PEPCK
Regulatory Monoubiquitination of Phosphoenolpyruvate Carboxylase in Germinating Castor Oil Seeds*S⃞♦
Phosphoenolpyruvate carboxylase (PEPC) is a tightly regulated enzyme
situated at the core of plant C-metabolism. Although its anaplerotic role and
control by allosteric effectors, reversible phosphorylation, and
oligomerization have been well documented in the endosperm of developing
castor oil seeds (COS), relatively little is known about PEPC in germinating
COS. The initial phase of COS germination was accompanied by elevated PEPC
activity and accumulation of comparable amounts of pre-existing 107-kDa and
inducible 110-kDa immunoreactive PEPC polypeptides (p107 and p110,
respectively). A 440-kDa PEPC heterotetramer composed of an equivalent ratio
of non-phosphorylated p110 and p107 subunits was purified from germinated COS.
N-terminal microsequencing, mass spectrometry, and immunoblotting revealed
that both subunits arose from the same gene (RcPpc3) that encodes the
p107 subunit of a phosphorylated 410-kDa PEPC homotetramer in developing COS
but that p110 is a monoubiquitinated form of p107. Tandem mass spectrometry
sequencing of a diglycinated tryptic peptide identified Lys-628 as p110's
monoubiquitination site. This residue is conserved in vascular plant PEPCs and
is proximal to a PEP-binding/catalytic domain. Incubation with a human
deubiquitinating enzyme (USP-2 core) converted the p110:p107 PEPC
heterotetramer into a p107 homotetramer while significantly reducing the
enzyme's Km(PEP) and sensitivity to allosteric activators
(hexose-Ps, glycerol-3-P) and inhibitors (malate, aspartate).
Monoubiquitination is a non-destructive and reversible post-translational
modification involved in the control of diverse processes such as
transcription, endocytosis, and signal transduction. The current study
demonstrates that tissue-specific monoubiquitination of a metabolic enzyme can
also occur and that this modification influences its kinetic and regulatory
properties