WASHINGTON
USDA-ARS, WHEAT GENETICS, QUALITY, PHYSIOLOGY AND DISEASE RESEARCH UNIT
Departments of Crop & Soil Sciences, Food Science and Human Nutrition, and Plant Pathology, Washington State University, Pullman, WA 99164, USA.
Camille M. Steber, M.K. Walker-Simmons, L.D. Holappa,
Benjamin Rangel, John Ray, Eric W. Storlie, Ryan Wagner, R.E.
Allan, Roland F. Line, Xianming Chen, Ramon Cu, Zhixin Shi, B.L.
Waldron, A.D. Fjeld, C.F. Morris, A.D. Bettge, H.C. Jeffers, G.E.
King, B. Patterson, D.A. Engle, M. Baldridge, B. Davis, R. Ader,
and J.A. Anderson.
Gibberellin-response genes.
Camille M. Steber.
A project has been initiated to identify GA-response genes in
wheat related to the SLEEPY1 gene of Arabidopsis.
The long-term goal of this project is to improve emergence and
crop stand establishment in semidwarf wheat.
Cold hardiness.
M.K. Walker-Simmons, L.D. Holappa, Benjamin Rangel, John Ray,
Eric Storlie, and Ryan Wagner.
A crown-freezing simulation test (LT50 tests) was developed that
can differentiate cold-hardy and nonhardy Pacific Northwest wheat
cultivars. New greenhouse and growth chamber facilities have enabled
us to develop freezing simulation tests for multiple breeding
samples. We have completed initial screening of cold hardiness
levels in the advanced and elite breeding lines of the ARS club
wheat breeding program.
A project was initiated to determine the effect of the Fr1Vrn1
interval and candidate genes on cold hardiness in wheat. In support
of this initiative, we are developing RILs derived from crosses
between cold-hardy and nonhardy cultivars and synthetic hexaploid
lines.
Signal transduction and protein kinases.
Wheat protein kinases that are expressed in dormant and
germinating wheat seeds are being characterized. The function
of PKABA1, an abscisic acid-responsive protein kinase mRNA isolated
from wheat embryos, was determined using a barley aleurone transient
gene assay. Constitutive expression of PKABA1 markedly suppresses
expression of low- and high-pI a -amylase and protease genes induced
by gibberellic acid in barley aleurone layers. These results indicate
that PKABA1 acts as a key intermediate in the signal transduction
pathway leading to the suppression of GA-inducible gene expression
in cereal aleurone layers.
Wheat seed proteins role in desiccation tolerance.
Heat-soluble proteins extracted from desiccation-tolerant
wheat seeds have been demonstrated to improve survival and function
of turkey sperm during storage. Our previous results have suggested
that the heat-soluble proteins serve as hydration buffers in wheat
seeds.
Publications.
Donoghue AM and Walker-Simmons MK. 1998. The influence of wheat
dehydration-induced proteins on thefunction of turkey spermatozoa
after 24 hours in vitro storage. Poultry Sci 78:235-241.
Gomez-Cadenas A, Verhey SD, Holappa LD, Shen Q, Ho T-H D, and
Walker-Simmons MK. 1998. An abscisic acid-induced protein kinase,
PKABA1, mediates abscisic acid-suppressed gene expression in barley
aleurone layers. Proc Natl Acad Sci USA 96:1767-1772.
Storlie EW, Allan RE, and Walker-Simmons MK. 1998. Effect of the
Vrn1-Fr1 interval on cold hardiness levels in wheat near-isogenic
lines. Crop Sci 38:483-488.
Storlie EW, Walker-Simmons MK, Anderson JA, and Allan RE. 1998.
Effect of the Fr1-Vrn1 interval on cold hardiness in wheat.
In: Proc 9th Inter Wheat Genet Symp (Slinkard AE ed). University
Extension Press, Saskatoon, Saskatchewan, Canada. 4:92-94.
Walker-Simmons MK. 1998. Protein kinases in seeds. Seed Sci Res
8:193-200.
Seed stocks of dominant, male-sterile, soft white winter wheat.
R.E. Allan.
A dominant, male-sterile gene that is putatively the Ms3
gene was transferred into six U.S. SWWW varieties. The varieties
were Madsen, Lewjain, Daws, and Stephens (SWWW commons), and Hyak
and Tres (SWWW clubs). Each of these varieties are currently or
were important varieties grown in the U.S. Pacific Northwest.
The varieties have attributes that should make them useful in
SWWW improvement. Hyak and Madsen have the Pch1 gene for
resistance to eyespot foot rot and have combined resistances to
stripe rust, leaf rust, and stem rust. Lewjain has excellent soft
white wheat quality, good tolerance to Cephalosporium stripe,
and very good nonrace-specific resistance to stripe rust. Daws
has very good cold hardiness and both race-specific and nonrace-specific
resistance to stripe rust. Stephens has wide adaptation, high-yield
potential, heavy kernel weight, and both race-specific and nonrace-specific
resistance to stripe rust. These varieties were registered in
Crop Science (Daws 17:4, 674; Stephens 18:6,
1097; Lewjain 23:5, 1014; Madsen 29:6, 1575; and
Hyak 30:1, 234). Additional information concerning these
varieties can be found in their registration statements. The original
germ plasm containing the dominant male-sterile gene was obtained
from P.S. Baenziger in 1983.
Pedigrees, crop year, percent germination, and percent sterility
of these F1 seed stocks are shown in Table 1.
Pedigrees | Percent | Crop year | |
---|---|---|---|
Sterility | Germination | ||
83I 1 Ms3/Tyee/3*Barbee/2*Tres//5-6*Hyak | 43 | 92 | 1993, 94 |
83I 1 Ms3/Tyee/3*Barbee//7*Tres | 40 | 90 | 1993 |
83I 1 Ms3/11-12*Daws | 50 | 98 | 1993, 94 |
83I 1 Ms3/9*Stephens | 47 | 92 | 1998 |
83I 1 Ms3/Daws//10-12*Lewjain | 41 | 98 | 1993, 94 |
83I 1 Ms3/3*Stephens//5-7*Madsen | 52 | 94 | 1993, 94, 95 |
Between 4 and 10 backcrosses were made to each variety. The club
varieties Barbee and Tyee appear in the pedigrees of the Hyak
and Tres seed stocks. Each genetic stock closely resembles the
phenotype of its recurrent parent. In the case of Hyak, Daws,
Lewjain, and Madsen, two or three different backcross generations
were bulked together to obtain sufficient amounts of seed.
Small amounts of seed of these stocks are available upon request
from bonafide wheat breeding and genetics programs. Seed of the
recurrent parents will not be distributed. Intercrossing male-fertile
plants with male-sterile plants within each seed stock will maintain
its genetic integrity. Seed supplies are limited and will be distributed
based on the date of request. Requests should be made to L.M.
Little: lmlittle@.wsu.edu; Fax: 509-335-2553.
Publications.
Allan RE. 1997. Agronomic performance of plant height near-isolines
of Nugaines wheat. Wheat Inf Serv 85:31- 34.
Schillinger WF, Donaldson E, Allan RE, and Jones SS. 1998. Winter
wheat seedling emergence from deep sowing depths. Agron. J 90:582-586.
Control of rusts and smuts in the western United States,
1998.
Roland F. Line, Xianming Chen, Ramon Cu, and Zhixin Shi.
Using predictive models and monitoring data, wheat stripe and
leaf rusts were accurately forecasted for the 20th and 16th consecutive
years, respectively. Stem rust was accurately forecasted based
on weather in June and July. Stripe rust continues to be the most
widely important wheat disease in the western United States. Leaf
rust is the second most widely important disease. In northwestern
Washington and western Oregon, the autumn, winter, and spring
environments were highly favorable for establishment, survival,
and increase of stripe rust and leaf rust; however, barley yellow
dwarf was so prevalent and severe that accurate recording of data
and assessment of the impact of therusts was not possible. In
eastern Washington and Oregon and northern Idaho, relatively wet
weather during the autumn, unusually warm temperatures during
the winter, and cool wet weather in April were favorable for establishment,
survival, and increase of stripe rust. Wetter than normal weather
in early July was favorable for stem rust in late-maturing fields
of winter wheat and spring wheat in the Palouse region of Washington
and northern Idaho. In California, the winter and spring weather
was favorable for stripe rust, and susceptible wheat and barley
cultivars were damaged by the disease.
In regard to potential rust for the 199899 growing season, the
autumn weather in 1998 and the winter weather in 199899 were highly
favorable for the establishment and survival of both stripe rust
and leaf rust in the western United States. If the early spring
is cool and wet, severe stripe rust in the western United States
is probable in 1999. If the later spring is wet, leaf rust could
be severe in the western United States.
The effects of naturally occurring stripe rust, leaf rust, and
stem rust on 32 winter wheat cultivars at sites near Walla Walla
and Pullman, WA, and on 20 spring wheat cultivars at sites near
Pullman were determined by comparing untreated plots with plots
sprayed with Folicur to control foliar diseases. Severity of the
diseases on the cultivars differed at the sites because of differences
in environment and pathogens. At Walla Walla, stripe rust and
leaf rust developed at a later stage of plant growth, but by the
hard-dough stage of growth in untreated plots of the most susceptible
cultivars, stripe rust had increased to 99 %, and leaf rust had
increased to 90 %. Stem rust occurred too late to affect yield
at Walla Walla. At Pullman, stripe rust began to increase at an
earlier growth stage and developed to 99 % by the soft-dough stage.
The rain in early July provided favorable weather for stem rust.
Leaf rust was less severe at Pullman. Losses caused by the rusts
at the sites ranged from 0 % to more than 70 % depending upon
resistance of the cultivars to the types and races of the pathogens.
Powdery mildew and Septoria caused no significant losses.
Stripe rust, leaf rust, stem rust, and other wheat diseases are
annually monitored in the western U.S. to determine their distribution,
prevalence, and severity and to determine the vulnerability of
cultivars to local races of the pathogens. Barley stripe rust,
which was introduced into North America from Europe by way of
South America and Mexico in 1991, has spread north and west from
Texas. The disease, now indigenous in the western U.S., has significantly
impacted barley yields in Colorado, Arizona, Utah, California,
Oregon, and Washington. We have clearly determined by pathogenicity
and RAPD analysis that the wheat stripe rust pathogen is different
from the barley stripe rust pathogen. The wheat stripe rust pathogen,
which attacks primarily wheat and triticale, can attack some barley
and rye cultivars, and the barley stripe rust pathogen, which
attacks primarily barley, can attack some wheat, triticale, and
rye cultivars. At least 59 wheat stripe rust races and 50 barley
stripe rust races have been detected in North America. In 1998,
the most prevalent wheat stripe rust races were those that were
virulent on Moro, Tres, Hatton, Weston, Westbred 470, Lee, Fielder,
Express, and Vanna; on seedlings of Stephens and Madsen; and on
cultivars developed in regions of the United States where stripe
rust does not normally occur. Stripe rust was most severe in fields
of Westbred 470 and Vanna in the Pacific Northwest and fields
of Express in California. The rust on Westbred 470 was not a new
race. Rust collections from Express and Vanna may be new races.
No new leaf rust or stem rust races were detected in the western
U.S. Powdery mildew, common bunt, flag smut, and dwarf bunt each
caused insignificant losses in the western United States, less
than 0.1 %. Karnal bunt, which is now present in Arizona, has
had an impact on marketing wheat. However, current evidence shows
that it has not spread to any new regions and reduced wheat yields
or affected the quality of flour in the region where it occurs.
Each year, we evaluate a new group of entries from the National
Small Grain Germplasm Collection for high-temperature, adult-plant
resistance to stripe rust in environmentally different field plots
at Mount Vernon and Pullman, WA, and for seedling resistance to
selected stripe rust races that include all of the virulences
that have been identified in North America. This information is
added to their database. Cultivars and breeding lines developed
by public and private breeders in the western United States also
are annually evaluated in field plots at various sites for resistance
to stripe rust and other diseases. Currently, most of the major
SWWW cultivars and spring wheat cultivars grown in the western
U.S. have high-temperature, adult-plant resistance, and their
resistance has remained durable against all North American races
of stripe rust. New lines with resistance to the rusts were identified,
and cultivars with superior resistance were released. High-temperature,
adult-plant resistance continues to be the most effective and
durable type of stripe rust resistance. In regions where stripe
rust occurs, high-temperature, adult-plant resistance has annually
prevented severe losses. Multiline cultivars developed in the
northwestern U.S. for stripe rustresistance also have remained
durable. The major club wheat cultivar grown in the state of Washington
has multiline resistance. Molecular markers associated with high-temperature,
adult-plant resistance genes in Stephens and resistant F8 progeny
from crosses with Stephens show possibilities as tools for identifying
plants with high-temperature, adult-plant resistance. Selection
for the markers associated with the high-temperature, adult-plant
resistance genes should be easier and faster than selecting for
high-temperature, adult-plant resistance by field testing advanced
generations of large populations. This should be especially valuable
in transferring high-temperature, adult-plant resistance into
club wheats.
We recently developed a technique for detecting molecular markers
for resistance genes that is referred to as Resistance Gene Analog
Polymorphism (RGAP). The RGAP technique requires less DNA; does
not require restriction enzymes and radioactive isotopes; and
is faster and more efficient, consistent, and more reliable than
other techniques. The RGAP technique was used to screen NILs with
stripe rust resistance genes Yr1, Yr5, Yr7,
Yr8, Yr9, Yr10, Yr15, Yr17,
Yr18, and YrA. We have identified at least one unique
RGAP maker (in some cases many more) for each gene. Four RGAP
markers were directly associated with Yr9, and two were
closely linked with Yr9. The four markers had sequence
similarities to disease-resistance genes in rice. A probe derived
from a Yr9 marker has the same kinase-gene pattern as a
probe for the leaf rust-resistance gene Lr10. Segregating
populations are being produced for mapping the 10 Yr genes.
The markers are being used to select for a combination of Yr5,
Yr8, Yr9, and Yr15, the most effective race-specific
genes in the U.S.
Fungicides are annually evaluated for control of stripe rust,
leaf rust, stem rust, common bunt, flag smut, dwarf bunt, and
other diseases. In 1998, seed treatments and foliar fungicides
were evaluated for control of stripe rust, leaf rust, and stem
rust in winter and spring wheat plots near Walla Walla, Mt Vernon,
and Pullman, WA. Treatment of seed with Baytan was most effective
in controlling stripe rust when used with foliar treatments but
of little value for control of leaf rust and stem rust. Foliar
applications of Folicur, Tilt, Quadris, Govern, BAS-500, and Tilt
+ CGA279202 controlled stripe rust, leaf rust, and stem rust when
applied according to various schedules. Effectiveness of the fungicides
in preventing crop losses depended upon the type and race of rust,
when the rust began to increase, susceptibility of the cultivars,
stage of plant growth when the sprays were applied, and the weather.
Applications early enough to prevent severe rust on the upper
foliage were most effective. Most of the foliar treatments protected
the crop for about 1 month. Protection from the boot to milk stage
prevented most losses caused by stripe rust and leaf rust. Protection
from the heading to soft-dough stage prevented most losses caused
by stem rust.
A computerized, expert system for predicting and managing rusts
and other diseases of wheat referred to by the acronym MoreCrop
(Managerial Options for Reasonable Economical Control of Rusts
and Other Pathogens) was developed in 1993. MoreCrop predicts
what diseases should be problems based on geographical regions;
agronomic zones; crop managerial practices (crop rotation, tillage
methods, irrigation, planting date, and fertilized use); cultivar
characteristics; prevailing weather; crop history; and disease
history; provides information, options, and suggestions for managing
the diseases; and provides a library with information about the
diseases. MoreCrop is currently being updated, modified, and expanded
to include new information on agronomic zones, 30 diseases and
their characteristics, additional crop managerial practices, additional
cultivars and their resistance, new seed treatments and foliar
sprays, and cost-benefit relationships. New, up-to-date computer
technology also will be utilized. The new version (MoreCrop 2.0)
should be available in the spring of 1999.
Publications.
Chen XM, Hayes PM, Toojinda T, Vivar H, Kudrna D, Kleinholfs A,
Leung H, and Line RF. 1998. Genetic mapping of genes for stripe
rust resistance in barley using resistance gene analog polymorphism
and AFLP markers. Phytopathology 88:S16 (Abstract).
Chen XM, and Line RF. 1998. Identification of genes for resistance
to Puccinia striiformis f. sp. hordei in 18 barley
genotypes using diallel Analysis. Phytopathology 88:S16
(Abstract).
Chen XM, Line RF, and Leung H. 1998. Resistance gene analogs associated
with a barley locus for resistance to stripe rust. Plant and Animal
Genome VI. Page 124 (Abstract).
Chen XM, Line RF, and Leung H. 1998. Recessive inheritance of
resistance in barley to races of Puccinia striiformis f.
sp. hordei. Phytopathology 87:S18 (Abstract).
Chen XM, Line RF, and Leung H. 1998. Genome scanning for resistance
gene analogs using high resolution electrophoresis. Phytopathology
87:S18 (Abstract).
Chen XM, Line RF, and Leung H. 1998. Recessive inheritance of
resistance in barley to races of Puccinia striiformis f.
sp. hordei. Phytopathology 87:S18 (Abstract).
Chen XM, Line RF, and Leung H. 1998. Genome scanning for resistance-gene
analogs in rice, barley, and wheat by high-resolution electrophoresis.
Theor Appl Genet 97:345-355.
Chen XM, Line RF, Shi ZX, and Leung H. 1998. Genetics of wheat
resistance to stripe rust. In: Proc 9th Inter Wheat Genet
Symp (Slinkard AE ed). University Extension Press, Saskatoon,
Saskatchewan, Canada. 3:237-239.
Line RF. 1998. Management of wheat diseases in the United States.
In: Proceedings of The National Wheat Industry Research
Forum, NAWG Foundation, Washington, DC. Pp. 88-89.
Line RF. 1998. Quarantines for control of flag smut of wheat:
are they effective or necessary? In: Bunts and Smuts of
Wheat: An international Symposium (Malik VS and Mathre DE eds).
North American Plant Protection Organization, Ottawa. Pp. 49-60
Line RF. 1998. Control of stripe rust of spring barley in western
Washington with foliar fungicides, 1997. Fungicide and Nematicide
Tests 53:283-284.
Line RF. 1998. Control of stripe rust of winter barley in western
Washington with foliar fungicides, 1997: Fungicide and Nematicide
Tests 53:285-286
Line RF. 1998. Control of stripe rust, leaf rust, and stem rust
of spring wheat with foliar fungicides, 1997. Fungicide and Nematicide
Tests 53:293-294
Line RF. 1998. Use of foliar fungicides to assess winter wheat
yield losses caused by stripe rust, leaf rust, stem rust, and
powdery mildew in eastern Washington, 1997. Fungicide and Nematicide
Tests 53:295-296.
Line RF. 1998. Control of stripe rust, and powdery mildew of winter
wheat in southeastern Washington with foliar fungicides, 1997.
Fungicide and Nematicide Tests 53:297-300.
Line RF. 1998. Control of stripe rust, leaf rust, stem rust, and
powdery mildew of winter wheat in eastern Washington with foliar
fungicides, 1997. Fungicide and Nematicide Tests 53:301-307.
Line RF. 1998. Use of foliar fungicides to assess spring wheat
yield losses caused by stripe rust, leaf rust, and stem rust in
eastern Washington, 1997. Fungicide and Nematicide Tests 53:308.
Line RF. 1998. Control of stripe rust and stem rust of spring
barley with seed treatments and foliar fungicides, 1997. Fungicide
and Nematicide Tests 53:383-384.
Line RF. 1998. Control of stripe rust of winter barley with seed
treatments and foliar fungicides, 1997. Fungicide and Nematicide
Tests 53:385-386.
Line RF. 1998. Control of flag smut of wheat with seed treatments,
1997. Fungicide and Nematicide Tests 53:418.
Line RF. 1998. Control of stripe rust, stem rust, and powdery
mildew of winter wheat with seed treatments and foliar sprays,
1997. Fungicide and Nematicide Tests 53:419-420.
Line RF. 1998. Control of stripe rust, leaf rust, and stem rust
of spring wheat with seed treatments and foliar sprays, 1997.
Fungicide and Nematicide Tests 53:421-422.
Line RF. 1998. Control of common bunt of wheat with seed treatments,
1997. Fungicide and Nematicide Tests 53:423
Shi ZX, Chen XM, Leung H, Wellings C, and Line RF. 1998. Development
of markers for genes resistance to stripe rust using genome scanning
for resistance gene analog polymorphism. Phytopathology 88:S81
(Abstract).
Mapping genes for resistance to Fusarium head blight.
J.A. Anderson, B.L. Waldron, and A.D. Fjeld.
Our current map of the 'Sumai 3/Stoa' population that was phenotyped
for FHB resistance in greenhouse studies consists of 360 RFLP
and 151 AFLP markers. Four genomic regions containing putative
QTLs were associated (P < 0.01) with FHB resistance
from the combined analysis of two experiments, two from Sumai
3 (chromosomes 3BS and 6BL) and two from Stoa (2AL and 4BL). The
two markers associated with FHB resistance from Sumai 3 in the
'Sumai 3/Stoa' population also were associated with resistance
in an 'ND2603 (Sumai 3/Wheaton)/Butte 86' population. In addition,
another RFLP marker associated with resistance from ND2603 on
chromosome 3AL was identified in this population. Loci associated
with FHB resistance from Stoa have not been mapped in 'ND2603/Butte
86' due to lack of polymorphism. Future research will focus on
i) mapping additional markers on 3BS and obtaining PCRable markers
for this region, ii) verifying these and other new markers in
other populations, and iii) utilizing the markers for selection.
Personnel changes.
Dr. James Anderson resigned his position as research geneticist
in July, 1998, and is now an assistant professor at the University
of Minnesota. Dr. Blair Waldron resigned his position as postdoctoral
associate in April, 1998, to accept a research geneticist position
with the USDAARS in Logan, UT.
Publications.
Anderson JA, Cox DJ, Moore W, Miller JD, Rasmussen JB,
and Francl LJ. 1998. Registration of 'Elkhorn' wheat. Crop Sci
38:1403.
Anderson JA, Waldron BL, Moreno-Sevilla B, Stack RW, and Frohberg
RC. 1998. Detection of Fusarium head blight resistance QTL in
wheat using AFLPs and RFLPs. In: Proc 9th Inter Wheat Genet
Symp (Slinkard AE ed). University Extension Press, Saskatoon,
Canada. 1:135-137
Anderson JA, Waldron BL, Moreno-Sevilla B, Stack RW, and Frohberg
RC. 1998. DNA markers for Fusarium head blight QTL in two wheat
populations. In: Proc 9th Inter Wheat Genet Symp (Slinkard
AE ed). University Extension Press, Saskatoon, Canada. 3:57-59.
Sorrells ME and Anderson JA. 1998. Registration of 'Cayuga' wheat.
Crop Sci 38:551-552.
Waldron BL, Anderson JA, Coyne C, Stack RW, and Frohberg RC. 1998.
AFLP mapping of QTL for Fusarium head blight resistance
in wheat. PAG VI Abstracts, San Diego, CA. p. 122.
USDA-ARS Western Wheat Quality Laboratory.
Wheat endosperm texture.
C.F. Morris, A.D. Bettge, H.C. Jeffers, G.E. King, B. Patterson,
D.A. Engle, M. Baldridge,
B. Davis, and R. Ader.
We have recently shown that wheat endosperm texture (soft or hard)
results from positive genetic control by the hardness locus (Ha)
on chromosome 5DS, a complex locus coding for puroindoline-a and
puroindoline-b, collectively known as friabilin. In the wild type,
both puroindolines are normal (functional) and result in soft
wheat. To produce hard wheat, one or the other puroindoline must
be nonfunctional. A single nucleic acid base change in puroindoline-b
causes a serine for glycine substitution at amino acid 46 and
leads to hard-textured wheat. A complete absence of puroindoline-a
(no transcript produced) also leads to hard-textured wheat. No
recombination between puroindoline-a and puroindoline-b has been
observed in several hundred genotypes examined to date. The puroindoline-b
type mutation has been observed in 90+ % of hard winter wheat
and half of hard spring wheat. The puroindoline-a type mutation
has been observed in < 10 % of hard winter wheat and half of
hard spring wheat.
Polyphenol oxidase (PPO) and Asian noodle discoloration.
We have developed laboratory-scale alkaline noodle tests to assist
in screening potential cultivars for suitability in Asian noodle
applications. The test uses 100 g of flour and an alkaline salt
solution to produce noodle sheets that are analyzed for color,
especially the L* value (of the L*a*b* scale) at 0 and 24 hr after
noodle production. The results provide information about the degree
of discoloration in noodles brought about by PPO.
Additionally, a buffered L-DOPA test for rapid, small-scale assessment
of PPO in single kernels has been developed. This test affords
rapid (about 1 hr), nondestructive assessment of PPO content at
early generations of wheat breeding programs and will assist breeders
in producing low-PPO wheat for use in Asian style noodles.
Noting that two current cultivars Daws and Centennial have bimodal
distributions of PPO content, we have used the L-DOPA PPO assay
to physically separate low-PPO from high-PPO kernels and are in
the process of increasing the low-PPO kernels as potential rereleased
improved cultivars.
Starch quality.
Another important attribute of Asian noodles is texture. To a
large extent, the texture of noodles and other products depends
on the amylose/amylopectin (AM/AP) ratio of starch. The AM/AP
ratio has an impact on water absorption during the gelatinization
process of cooking and this impacts end quality and processing
factors. The AM/AP ratio results from the action of granule-bound
starch synthase. Apparent amylose content varies from about 22
% (0-gene waxy) to 0 % (3-gene waxy).
We have characterized the starch gelatinization/gelation properties
of 0, 1, 2, and 3-gene waxy-state wheats and wheat flours using
flour swelling volume and RVA tests and linked these results to
end-use attributes.
Cultivar development program.
Our cultivar development program screened over 8,000 experimental
breeding lines for milling and baking quality and provided the
results to wheat breeders for use in their programs.
The WWQL-led PNW Wheat Quality Council held a forum to discuss
potential new cultivars and the comments and concerns about wheat
quality issues. The forum in Bozeman, MT, was attended by about
45 people representing growers, researchers, breeders, marketers,
and end-users.
Personnel changes.
Morten Lillemo, from the Agricultural University of Norway, has
joined the WWQL for 9 months of research on puroindoline-a and
puroindoline-b wheat hardness effects in northern European wheats.
Dr. Tigst Demeke, formerly of Saskatoon, Saskatchewan, Canada,
has joined the WWQL as a post-doctoral research associate to pursue
research into PPO biochemistry and its genetic underpinnings.
Publications.
Giroux MJ, Babb S, and Morris CF. 1998. Wheat grain hardness is
controlled by highly conserved puroindoline mutations. In:
Prog Abstr Plant & Animal Genome IV (Grant D and Lazo G eds).
Scherago Intl Publish. p. 119.
Giroux MJ and Morris CF. 1998. Wheat grain hardness results from
highly conserved mutations in the friabilin components puroindoline
a and b. Proc Natl Acad Sci USA 95:6262-6266.
Morris CF. 1998. Genetic determinants of wheat grain quality.
In: Proc 9th Inter Wheat Genet Symp (Slinkard AE ed). University
Extension Press, Saskatoon, SK, Canada. 1:245-253.
Morris CF. 1998. Evaluating the end-use quality of wheat breeding
lines for suitability in Asian noodles. In: Pacific People
and Their Food (Blakeney AB and O'Brien L eds). American Association
of Cereal Chemists, St. Paul, MN. pp. 91-100.
Morris CF. 1998. Assessing hard white wheat samples for end-use
quality. In: Proc 21st Hard Winter Wheat Workers Workshop
(Peterson CJ ed). USDAARS and Colorado State Univ. pp. 75-77.
Morris CF, Bettge AD, Giroux MJ, Zeng M, and King GE. 1999. Relationships
between RVA pasting characteristics and amylose content of normal,
partially-waxy, and waxy wheat flours and starches. In:
RACI/AACC Symposium, Cairns, Australia. (In press).
Morris CF, DeMacon VL, and Giroux MJ. 1999. Phenotypic expression
of and methods of measuring wheat grain hardness among chromosome
5D homozygous recombinant substitution lines. Cereal Chem (In
press).
Allan RE, Morris CF, Line RF, Anderson JA, and Donaldson E. 1999.
Registration of 'Coda' club wheat. Crop Sci (In press).
Kidwell KK, Shelton GS, Morris CF, Line RF, Miller, BC, Davis
MA, and Konak CF. 1999. Registration of 'Scarlet' wheat. Crop
Sci (In press).
Morris CF, Jeffers HC, and Engle DE. 1999. Effect of processing,
formula and measurement variables on alkaline noodle color - towards
an optimized system. Cereal Chem (Submitted).
Morris CF and Konzak CF. 1999. Registration of D-null 'Bai Huo'
waxy wheat germplasm. Crop Sci (Submitted).
Morris CF, Bettge AD, Giroux MJ, Zeng M, and King GE. 1998. Relationships
between RVA pasting characteristics and amylose content of normal,
partially-waxy, and waxy wheat flours and starches. In:
Pacific People and Their Food (Blakeney AB and O'Brien L eds).
American Association of Cereal Chemists, St. Paul, MN. pp. 75-76.
Morris CF, Anderson JV, Bettge AD, and Correll ME. 1998. Distribution
of PPO activity among a large number of hexaploid wheat genotypes
using an improved L-DOPA assay. Cereal Foods World 43:518.
Morris CF, Lukow OM., and Perron CE. 1998. Grain hardness, dough
mixing and pan bread performance among wheats differing in puroindoline
hardness mutation. Cereal Foods World 43:533.
WASHINGTON STATE UNIVERSITY
Spring Wheat Breeding and Genetics Program, Department of Crop and Soil Sciences, 201 Johnson Hall, Pullman, WA 99164-6420, USA.
Overview of cultivar development and genetic mapping efforts.
K. Kidwell, B. Barrett, V. DeMacon, and G. Shelton.
Nearly 400 crosses were made in 1998, and early generation soft
white, hard red, hard white, and spring club germ plasms with
novel Hessian fly and RWA-resistance genes were advanced to the
field-breeding program. F1 seed from 395 lines was increased to
generate segregating progenies for use in conventional breeding
strategies, marker-assisted selection, and gene linkage analyses.
Seed-storage protein and polyphenol oxidase analyses were used
to select progeny with superior end-use quality potential for
advancement. Progress was made towards developing PCR-based tags
for genes associated with strawbreaker foot rot resistance, RWA
resistance, and Vrn2. Efforts were initiated to identify
potential gene donors for Rhizoctonia resistance among
wild relatives of wheat, and the feasibility of developing spring
wheat hybrids via inter-growth habit cross-hybridizations are
under investigation. Approximately 695 F2 and 610 F3 families
were advanced to the next generation, and 2,972 entries among
16,492 F4 and 23,394 F5 head rows were selected, based on stripe
rust reaction and phenotype, for early generation end-use quality
assessment. Approximately 700 lines with superior end-use quality
potential will be advanced to 1999 field trials. Nine-hundred
twelve F6, 216 F7, and 128 advanced lines (F8+) were evaluated
at three to 15 locations under annual crop, crop/fallow, and irrigated
conditions. Grain samples from 474 experimental lines with superior
agronomic performance were sent to the Western Wheat Quality Laboratory
for milling and baking tests.
Variety releases and advanced lines with potential for release.
K. Kidwell, G. Shelton, V. DeMacon, C. Morris, and C.
Konzak.
Scarlet HRSW was approved for final release as a replacement
for Butte 86 in the semi-arid, nonirrigated wheat production region.
Scarlet is moderately resistant to stripe rust but is susceptible
to the Hessian fly. Based on 5-year averages, Scarlet produces
from 5 to 10 bu/acre more grain than Butte 86 and Westbred 926,
depending on location. Test weight of grain from Scarlet is 0.5
to 1 lb/bu lower than that of Butte 86 and equal to that of Westbred
926. Typically, grain protein content of Scarlet is similar to
or higher than that of Butte 86 in the targeted production region.
However, protein content of Scarlet tends to be 0.4 % to 0.6 %
lower than those of Butte 86 and Westbred 926 when grown in locations
receiving more than 14 inches of annual precipitation. Foundation
seed of Scarlet will be available for spring planting in 1999.
The soft white experimental line WA7850 was approved for
variety release as a replacement for Alpowa, Penawawa, and/or
Wawawai. WA7850 has outstanding grain yield potential and end-use
quality properties. This variety is stripe rust resistant, and
preliminary data indicate that it also is resistant to the Hessian
fly. The proposed name for this variety is Zak, and breeders'
seed will be produced in 1999.
WA7824, a HRSW with exceptional gluten strength, was approved
for preliminary seed increase. WA7824 is resistant to stripe rust
and, preliminary results indicate that it is resistant to the
Hessian fly. WA7824 has higher grain-yield potential and a higher
test weight than of Westbred 926. However, the grain protein contentof
WA7824 is slightly lower than that of Westbred 926. Based on milling
and baking data generated by the Western Wheat Quality Laboratory
and members of the PNW Quality Council, the end-use quality of
WA7824 is superior to that of most HRSW varieties in commercial
production in the PNW. Fertility trials are being conducted to
develop management strategies to increase the grain protein content
of WA7824. If the Hessian fly resistance is confirmed, WA7824
will be proposed for variety release in 2000.
Early generation, end-use quality assessment of wheat grain
from F4 and F5 head rows.
K. Kidwell, C. Morris, V. DeMacon, G. Shelton, and D. Engle.
Following phenotypic selection, grain from selected head rows
(~2,800) was visually evaluated for plumpness. Selections with
sound grain were separated by market class, then entries from
each market class were subjected to a specific assessment strategies
depending on end-use goals. Grain protein content and grain hardness
were determined on whole grain flour using the Technicon (NIR).
Microsedimentation and flour-swelling volume were used to assess
the end-use quality potential of selected lines. The microsedimentation
test is used to assess protein quality and gluten strength, whereas
the flour-swelling volume test produces starch swelling values
that are highly associated with noodle quality. Polyphenol oxidase
levels also were determined for soft white and hard white materials
to assess noodle color potential before selecting lines to be
advanced to 1999 field trials.
Enhancing heterosis of hybrid wheat via inter-growth habit
cross-hybridizations.
K. Kidwell, B. Barrett, and D.B. Cooper.
Utilizing heterosis by developing high yielding, hybrid, spring
wheat cultivars suitable for replacing erosion-prone winter wheat
production is a viable genetic solution to a major environmental
problem. A strategy to enhance grain yield potential of spring
cultivars by capitalizing on heterosis between spring and winter
wheat germ plasm pools via inter-growth habit crosses is described
in this proposal. The objectives are to: 1) examine heterotic
and maternal effects on F1 hybrids generated through intra- and
inter-growth habit crosses using full diallel analyses; 2) determine
the cold hardiness levels of wheat hybrids compared to their inbred
parents; 3) assess heterotic and maternal effects on end-use quality
properties of F2 wheat grain; and 4) examine the relationship
between targeted DNA marker-based genetic diversity estimates
and heterosis in hybrid wheat. Based on previous results, four
elite spring and four elite winter cultivars were selected as
parents for F1 hybr