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Studies on the pectin network of the tomato fruit cell wallTibbits, C. William January 2000 (has links)
No description available.
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The effect of high temperature on lycopene synthesis and degradation in tomato fruit (Lycopersicon esculentum)Boothman, Stuart Roy January 1997 (has links)
No description available.
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Polyphenol oxidase, dopamine content, and discoloration in ripening bananasNandi, Bina Rani 04 June 1971 (has links)
Graduation date: 1972
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The effect of cultivar maturity and frozen storage time on the cell wall polysaccharide composition of muskmelon(Cucumis melo)Simandjuntak, Valencius 08 July 1993 (has links)
The effect of frozen storage time on the composition
of the cell wall polysaccharide (CWP) of muskmelon (Cucumis
melo) cultivars at different stages of maturity was investigated.
Changes in composition, firmness, drip loss, and
color of Cantaloupe and Honey Dew melon flesh were determined
at three stages of maturity and for three periods of
storage at -23°C. Relationships between firmness, drip
loss, and other composition measurements, as well as the
total CWP sugar composition, were also determined.
Cell wall polyssacharides were isolated and purified,
and fractionations were performed using cyclohexane trans-
1,2-diamine tetraacetate (CDTA), Na₂C0₃, guanidinium thiocyanate
(GTC), and KOH. All fractions and residues were
dialysed and then freeze-dried. Following hydrolysis of
CWP fractions with trifluoroacetate (TFA), the alditol acetate derivatives of neutral sugars from each CWP fraction
were prepared and analyzed by gas chromatography,
using myo-inositol as the internal standard.
TFA insoluble fractions were analyzed colorimetrically
using phenol-sulphuric acid reagent. Uronic acid was determined
using 0.15% m-hydroxybiphenyl for absorbance at
520 nm with galacturonic acid as the standard. It was determined
that CDTA and Na₂C0₃ fractions were composed of
typical pectic materials, containing mostly galacturonic
acid with the neutral sugars arabinose, galactose, rhamnose,
and a smaller amount of xylose. As maturity increased,
CDTA fraction yields increased, though total neutral
sugar CWP compositions decreased. GTC and KOH fractions
were typical of hemicellulose, and contained principally
xylose, glucose, galactose, mannose, and fucose, with very
small amounts of uronic acid, arabinose, and rhamnose.
Residue fractions contained principally glucose and galactose,
with smaller amounts of mannose, xylose, arabinose,
and fucose. With the exception of xylose and glucose, all
neutral sugars decreased significantly (p < 0.01) as maturity
increased in both the Cantaloupe and Honey Dew melons.
Total uronic acid did not change as maturity increased,
except for Cantaloupe, where total uronic acid decreased
from the ripe to overripe stages. The CDTA fraction
yield increased and all neutral sugars decreased
significantly (p < 0.05) as storage time was increased.
Only the CDTA fraction yield was negatively correlated with the firmness of both melons, and was positively correlated
with drip loss as maturity and frozen storage time were increased.
Firmness was positively correlated with Na₂C0₃ and
GTC fraction yield in Cantaloupe, whereas for Honey Dew
there was no correlation between firmness and Na₂C0₃ or GTC
fraction yield as maturity increased. The KOH fraction was
negatively correlated with firmness in Cantaloupe, whereas
there was no correlation between firmness and KOH fractions
in Honey Dew existed as maturity increased. The residue
fractions increased in both melons only from the underripe
to the ripe stages, and did not change from ripe to overripe.
Firmness was positively correlated with total rhamnose,
arabinose, mannose, and galactose as maturity increased,
and the drip loss was negatively correlated with
all total neutral sugars as storage time was increased.
During frozen storage, there was a significant decreases
(p < 0.05) in total CWP sugars in relation to increased
storage time. The decrease in total sugars was
more dramatic during the 0 to 5 month period than the 5 to
10 month period of frozen storage. Galactose did not
change in the Cantaloupe, whereas in Honey Dew it decreased
34.3% from 0 to 5 months then decreased only 13% from 5 to
10 months of storage. / Graduation date: 1994
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The role of endo-#beta#-1,4-glucanase in strawberry fruit developmentWoolley, Lindsey C. January 2000 (has links)
No description available.
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The role of a ripening-induced Rab11a GTPase in tomato (Lycopersicon esculentum Mill.) developmentLu, Chungui January 1999 (has links)
No description available.
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Analysis of transgenic tomato plants with acc oxidase suppressed by sense constructsAlphuche-Solis, Angel Gabriel January 1999 (has links)
No description available.
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The effects of aminoethoxyvinylglycine (AVG) and 1-methylcyclopropene (1-MCP) on banana ripening26 May 2010 (has links)
M.Sc. / Bananas are climacteric fruit which are characterised by a low rate of ethylene production and respiration during the pre-climacteric phase, followed by a sudden burst in ethylene production and respiration during ripening. Ethylene is a gaseous plant hormone that accelerates the ripening of climacteric fruit. In order to extend the shelf life of bananas the action or synthesis of ethylene must be inhibited or delayed. Examples of such inhibitors are 1- methylcyclopropene (1-MCP) an inhibitor of ethylene action, and aminoethoxyvinylglycine (AVG), an inhibitor of ethylene synthesis. The purpose of this research was to compare the effect of these two inhibitors on ripening of bananas. 1-MCP acts by blocking the ethylene receptors permanently. The results of this study indicated that 500 nL.L-1 1-MCP is more effective in delaying ripening of banana than AVG, although AVG delivered a better quality fruit in terms of colour. To be effective, bananas must be pre-treated with 1-MCP before they exposed to ethylene. The results also indicated that, the effectiveness 1-MCP to delay ripening decreases with storage time. The results show that ethylene binding to its membrane bound receptors is reversible if the exposure time to ethylene is less than 8 hours. Exposure to ethylene for 8 hours or more results in irreversible binding. However, binding only becomes permanent when exposure to ethylene exceeds 16 hours. For this reason treatment with 1-MCP becomes ineffective after exposure to ethylene for 24 hours due to the fact that ethylene has bound irreversibly and permanently to its binding sites and cannot be displaced by 1-MCP.
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Maturação induzida, alterações fisiológicas, produtividade e qualidade tecnológica da cana-de-açúcar (Saccharum officinarum L.)Leite, Glauber Henrique Pereira [UNESP] 20 June 2005 (has links) (PDF)
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leite_ghp_me_botfca.pdf: 653749 bytes, checksum: d0d894254b462b26f17369f46012f018 (MD5) / Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) / O projeto de pesquisa teve por objetivo avaliar as alterações fisiológicas na cana-de-açúcar decorrente da aplicação de maturadores químicos com diferentes mecanismos de ação e os reflexos na produtividade e qualidade tecnológica. Dessa forma foram instalados e conduzidos dois experimentos em cana soca nas Fazendas São Joaquim e Bosque, situadas no município de Igaraçú do Tietê, Estado de São Paulo, pertencentes ao Grupo COSAN - Unidade Barra (Usina da Barra). O delineamento experimental utilizado foi o em blocos casualizados com cinco repetições. No experimento 1 (Fazenda São Joaquim) utilizou-se a variedade de cana-de-açúcar RB855453 e no Experimento 2 (Fazenda Bosque) a variedade SP80-3280. Os tratamentos consistiram na aplicação de sete maturadores químicos (KNO3 (p.c. Krista Kana), Etil-trinexapac (p.c. Moddus), Sulfometuron metil (p.c. Curavial), Etefon (p.c. Ethrel), KNO3 + boro (p.c. Krista Kana Plus), Glifosato (p.c. Roundup) e Compostos de radicais carboxílicos orgânicos + Glifosato (p.c. MTD + Roundup)) e uma testemunha, maturação natural. As doses empregadas foram, respectivamente: 3 kg p.c. ha-1, 0,8 L p.c. ha-1, 20 g p.c. ha-1, 2 L p.c. ha-1, 3,0 kg p.c. ha-1, 0,4 L p.c. ha-1 e 1,0 L p.c. ha-1 + 0,15 L p.c. ha-1. A aplicação dos maturadores ocorreu nos meses de março (Experimento 1) e maio (Experimento 2) de 2004, utilizando-se equipamento costal pressurizado (CO2). As parcelas foram constituídas de 8 linhas de 10m de comprimento com espaçamento de 1,5m. Foram avaliados os seguintes parâmetros bioquímicos, biométricos e tecnológicos: atividade das enzimas invertases ácida solúvel e neutra em caldo de cana; altura de plantas, diâmetro dos colmos, número de colmos, rebrota, florescimento, chochamento, brotação lateral, produtividade de colmos e açúcar; pH, acidez, pol, pureza... / The purpose of research was to evaluate physiological alterations in sugarcane due to the application of chemical compounds with different actions and its reflects in the productivity and technological quality. Two experiments were carried out in ratoon cane in São Joaquim Farm and Bosque Farm, in Igaraçú do Tietê, São Paulo State, Brazil, belonging to Grupo COSAN - Unidade Barra (Usina da Barra). The experimental design used was random blocks with five repetitions. In experiment one (São Joaquim Farm) sigarcane RB855453 was used, and in experiment two (Bosque Farm) sugarcane SP80-3280. The treatments consisted of seven chemical compounds (potassium nitrate (trademark Krista Kana), Ethyl-trinexapac (trademark Moddus), Sulfometuron methil (trademark Curavial), Ethephon (trademark Ethrel), potassium nitrate + boron (trademark Krista Kana Plus), Glyphosate (trademark Roundup) and compounds of organic carboxilic radicals + Glyphosate (trademark MTD + Roundup)), and one control. The doses were, respectively: 3.0 kg ha-1 Potassium nitrate, 0.8 L ha-1 Ethyl-trinexapac, 20 g ha-1 Sulfometuron methil, 2.0 L ha-1 Ethephon, 3.0 kg ha-1 KNO3 + Boro, 0.4 L ha-1 Glyphosate, 1.0 L ha-1 Comp. carboxílicos + 0.15 ha-1 Glyphosate. The applications of chemicals were performed in March (Experiment one) and in May (Experiment two) in 2004, with constant spraying pressure... (Complete abstract, click electronic address below)
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Observations of Pituitary Hormone Injections and Ripening of FishKaushik, D. K. 01 May 1961 (has links)
A dependable source of quality fish spawn is a fundamental prerequisite for fish culture development. This is especially important inasmuch as most of the cultivable species do not breed in confined waters. Also, sport fisheries are gaining greater popularity, and subsequently the fish supply is being taxed. Still another need for fish spawn is in the ever increasing demand for bait minnows. Also, the construction of more and more dams has resulted in insurmountable obstacles for ascending and descending fish, which may ultimately result in complete destruction of some fisheries. Thus some measure of artificial propagation will have to be taken to safegaurd our valuable fishery resources.
A partial solution to this problem of supplementing natural propagation is that of inducing the fish to spawn artificially in the hatchery. A method of doing this is by stimulating fish to breed by the use of pituitary hormones. Those pituitary hormone-containing glands are often collected under a variety of field conditions which may involve considerable effort, time, and money. Therefore,, it was my objective in this study to develop a practical refined assay on hormones using as small an amount as possible of the crude extract of pituitary suspension, and to make it simple enough that every lay fisheries man ,dll be able to apply it, thus meeting his demand for quality fish eggs in his own hatchery when he needs it most.
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