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Plant Physiol, March 2003, Vol. 131, pp. 1159-1160
THE HOT AND THE CLASSIC
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RAFFINOSE OLIGOSACCHARIDES |
Raffinose family
oligosaccharides (RFOs) are -galactosyl derivatives of Suc. The most
common RFOs are the trisaccharide raffinose, the tetrasaccharide
stachyose, and the pentasaccharide verbascose. RFOs are nearly
ubiquitous in the plant kingdom and are found in a large variety of
seeds from many different families. They are components of the
carbohydrate reserves of many seed types, ranking second only to Suc in
abundance as soluble carbohydrates. RFOs accumulate during seed
development and disappear rapidly during germination. Because
-galactosidic linkages are not cleaved by human digestion,
flatulence often results after the consumption of RFO-rich seeds.
Because legume seeds are particularly rich sources of RFOs, RFO-induced
flatulence reduces the acceptance and nutritional benefits of grain
legumes. RFOs may also play a role in desiccation tolerance during seed
maturation. More recently, there has been accumulating evidence that
RFOs may play a role in protecting vegetative plant parts to
dehydrating stresses.
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Flatulence Promoters |
RFOS are found at especially high concentrations in legume
seeds. Due to the absence of -galactosidase activity in human and
animal intestine mucosa, RFOs escape digestion and are metabolized by
bacteria to hydrogen, carbon dioxide, and methane. Thus, RFOs have been
identified as the principal flatulence-causing factors present in
legumes and other seeds (Naczk et al., 1997 ). The
commercial product Beano (GlaxoSmithKline, Middlesex,
UK) advertised as a social and scientific breakthrough)
supplies -galactosidase and sucrase and helps prevent intestinal gas
by catalyzing the hydrolysis of these complex sugars. Flatulence is no
laughing matter: this problem is the single most important factor that
deters people from eating more legumes (Delumen, 1992 ).
The problem of legume seed-induced flatulence affects not just humans,
but all monogastric animals. Because of RFOs, the quantity of soybean
meal, for example, must be limited in animal feeds to avoid flatulence
in dogs (Canis familiaris) and digestive disturbances in
baby pigs (Sus scrofa) and chicks (Gallus
domesticus) (Hartwig et al., 1997 ). Various methods have been recommended for the removal of flatulence-inducing RFOs, including dehulling, soaking and/or cooking in water and in
buffer solutions, irradiation, enzymatic treatment, germination, and
solvent extraction (Naczk et al., 1997 ). Although a
reduction in RFOs is desirable from a nutritional perspective, it is
possible that if they become too low, the seed may have reduced
desiccation tolerance and storability. Consequently, plant biologists
have been searching for other desiccation-protecting factors such as galactosyl cyclitols that might substitute for RFOs in promoting desiccation tolerance but without having the unwanted anti-nutritional side effects of RFOs (Horbowicz and Obendorf,
1994 ).
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Seed Desiccation and Storability |
RFOs have been implicated in the protection of seeds against
damage during seed dehydration and aging, and therefore in seed survival and storability (Obendorf, 1997 ). RFOs may
protect membranes, proteins, and nucleic acids against the damage that
occurs during and upon the withdrawal of water in the drying seeds.
This protective role of oligosaccharides has been explained mainly by
their capacity to retain the integrity of membranes through their
interaction with the phospholipid headgroups, thus replacing water
during dehydration (Bentsink et al., 2000 ). It has also
been suggested, however, that RFOs may form a viscous glassy state (a
thermodynamically unstable solid state with an extremely high
viscosity) during seed dehydration. It has been hypothesized that this
glassy state may serve as a physical stabilizer protecting against
deteriorative reactions. RFOs, in particular, have been shown to have
an excellent ability to form stable glasses, and therefore
have been considered to be major determinants of seed storability
(Koster and Leopold, 1988 ). Indeed, the presence of
glasses has been associated with improved seed storage stability
(Sun and Leopold, 1997 ), and the content of raffinose in
maize (Zea mays) seeds is positively correlated with
both storage stability and the magnitude of the glassy state (Bernal-Lugo and Leopold, 1995 ). Nevertheless, a
causal role, if any, for RFOs, in contributing universally to
desiccation tolerance is unclear, and several recent studies have
clouded the issue even more.
To examine the role of RFOs in promoting the vitreous state and seed
storage stability, Buitink et al. (2000) took advantage of the fact that osmo-priming (the pre-imbibition of seeds in osmotic
solution) changes the oligosaccharide composition of seeds. Seed
priming improves seed quality by enhancing germination rates and
seedling uniformity, but has the drawback of reducing seed longevity by
unknown means. The authors used a spin probe technique to measure the
molecular mobility and glass transition temperature of the cytoplasm of
impatiens (Impatiens walleriana) and bell pepper
(Capsicum annuum) seeds that had been osmo-primed or
not. They found that the rotational correlation time of the polar spin probe in the cytoplasm decreased, together with seed longevity, as a
function of increasing seed water content, suggesting that longevity
may indeed be regulated by cytoplasmic mobility. As expected,
osmo-priming of the seeds resulted in considerable decreases in
longevity and the oligosaccharide content. There was no difference, however, in the rotational motion of the spin probe in the cytoplasm between control and primed impatiens and bell pepper seeds. They concluded, therefore, that oligosaccharides in seeds do not affect the
stability of the intracellular glassy state.
Based on their studies of a desiccation-intolerant, ABA-deficient
Arabidopsis mutant, Ooms, Wilmer, and Karssen (1994)
also concluded that RFOs are not the primary factor determining
desiccation tolerance in Arabidopsis seeds. Desiccation tolerance can
be induced in this ABA-deficient mutant in vivo by supplying an
ABA-analog to the plant root system, but this increase in desiccation
tolerance is not accompanied by significant changes in the carbohydrate composition of the seeds. The research of Bentsink et al.
(2000) also casts doubt on the importance of RFOs in
seed desiccation in Arabidopsis. These authors analyzed the soluble
oligosaccharides (Suc, raffinose, and stachyose) content in the seeds
of several Arabidopsis accessions and identified a genotype that had a
very low content of these carbohydrates. By performing (QTL) mapping in
a recombinant inbred line population, they identified one major QTL
responsible for the near monogenic segregation of seed stachyose content. This locus also affected the content of Suc and raffinose. A
comparison of the QTL genetic positions revealed that the genomic region containing the major oligosaccharide locus did not significantly affect seed storability. They concluded that in Arabidopsis neither RFOs nor Suc content has a major effect on seed storability.
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RFOs in Drought- and Cold-Stress in Vegetative Plant
Parts |
RFOs have been proposed to serve as osmoprotectants when
plants are exposed to environmental water deficit stresses, such as
cold and desiccation. Taji et al. (2002) found that
drought-, high salinity-, and cold-treated Arabidopsis plants
accumulate a large amount of raffinose and galactinol, but not
stachyose. Raffinose and galactinol were not detected in unstressed
plants. This suggests that raffinose and galactinol are involved in
tolerance to drought, high salinity, and cold stresses. They identified three stress-responsive galactinol synthase (GolS) genes
(AtGolS1, 2 and 3) among
seven Arabidopsis GolS genes. (GolS catalyzes the first
step in the biosynthesis of RFOs from UDP-Gal). AtGolS1 and 2 were induced by drought and high-salinity
stresses, but not by cold stress, whereas AtGolS3 was
induced by cold stress but not by drought or salt stress. The
overexpression of AtGolS2 caused an increase in
endogenous galactinol and raffinose, and reduced transpiration. These
results show that stress-inducible GolS plays a key role in the
accumulation of galactinol and raffinose under abiotic stress
conditions, and that galactinol and raffinose may function as
osmoprotectants during drought-stress in plants.
Liu et al. (1998) also presented several diverse
lines of evidence that suggest a role for RFOs in drought- and
cold-tolerance. They report that GolS activity increased in kidney bean
(Phaseolus vulgaris) seeds upon exposure of plants to
cold. Moreover, GolS mRNA levels in the vegetative
tissues of Arabidopsis increased significantly upon cold exposure, and
these transcripts diminished upon return of the plants to room
temperature. Finally, they established by protein sequence comparison
that a previously unidentified gene belonging to a group of
ABA-independent, desiccation stress inducible genes isolated from rice
(Oryza sativa) encodes the rice homolog the
GolS gene.
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FOOTNOTES |
www.plantphysiol.org/cgi/doi/ 10.1104/pp.900066.
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LITERATURE CITED |
-
Bentsink L, Alonso-Blanco C, Vreugdenhil D, Tesnier K, Groot SPC, Koornneef M
(2000)
Genetic analysis of seed-soluble oligosaccharides in relation to seed storability of Arabidopsis.
Plant Physiol
124: 1595-1604[Abstract/Free Full Text]
-
Bernal-Lugo I, Leopold AC
(1995)
Seed stability during storage - raffinose content and seed glassy state.
Seed Sci Res
5: 75-80
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Buitink J, Hemminga MA, Hoekstra FA
(2000)
Is there a role for oligosaccharides in seed longevity? An assessment of intracellular glass stability.
Plant Physiol
122: 1217-1224[Abstract/Free Full Text]
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Delumen BO
(1992)
Molecular strategies to improve protein-quality and reduce flatulence in legumes - a review.
Food Struct
11: 33-46
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Hartwig EE, Kuo TM, Kenty MM
(1997)
Seed protein and its relationship to soluble sugars in soybean.
Crop Sci
37: 770-773[Abstract/Free Full Text]
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Horbowicz M, Obendorf RL
(1994)
Seed desiccation tolerance and storability: dependence on flatulence-producing oligosaccharides and cyclitols.
Seed Sci Res
4: 385-405
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Koster KL, Leopold AC
(1988)
Sugars and desiccation tolerance in seeds.
Plant Physiol
88: 829-832[Abstract/Free Full Text]
-
Liu JJJ, Krenz DC, Galvez AF, de Lumen BO
(1998)
Galactinol synthase (GS): increased enzyme activity and levels of mRNA due to cold and desiccation.
Plant Sci
134: 11-20[CrossRef]
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Naczk M, Amarowicz R, Shahidi F
(1997)
alpha-galactosides of sucrose in foods: Composition, flatulence-causing effects, and removal.
ACS Symp Ser
662: 127-151
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Obendorf RL
(1997)
Oligosaccharides and galactosyl cyclitols in seed desiccation tolerance.
Seed Sci Res
7: 63-74
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Ooms JJJ, Wilmer JA, Karssen CM
(1994)
Carbohydrates are not the sole factor determining desiccation tolerance in seeds of Arabidopsis thaliana.
Plant Physiol
90: 431-436[CrossRef]
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Sun WQ, Leopold AC
(1997)
Cytoplasmic vitrification acid survival of anhydrobiotic organisms.
Comp Biochem Physiol A-Physiol
117: 327-333[CrossRef]
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Taji T, Ohsumi C, Iuchi S, Seki M, Kasuga M, Kobayashi M, Yamaguchi-Shinozaki K, Shinozaki K
(2002)
Important roles of drought- and cold-inducible genes for galactinol synthase in stress tolerance in Arabidopsis thaliana.
Plant J
29: 417-426[CrossRef][ISI][Medline]
Peter V. Minorsky
Department of Natural Sciences Mercy College Dobbs Ferry, NY 10522
© 2003 American Society of Plant Biologists
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