Hector Nuñez-Palenius

Dr. Hector Nuñez-Palenius


Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
14 December 2010 in Plant Cell Reports
Verified
Journal Article
Closed access
PDF file
CACesar Aza-González
Cesar Aza-González
Hector Nuñez-PaleniusHector Nuñez-Palenius
Hector Nuñez-Palenius
NONeftalí Ochoa-Alejo
Neftalí Ochoa-Alejo

1 January 2008 in Critical Reviews in Biotechnology
Verified
Journal Article
Closed access
Hector Nuñez-PaleniusHector Nuñez-Palenius
Hector Nuñez-Palenius
MGMiguel Gomez-Lim
Miguel Gomez-Lim
NONeftalí Ochoa-Alejo
Neftalí Ochoa-Alejo
RGRebecca Grumet
Rebecca Grumet
GLGene Lester
Gene Lester
DCDaniel J. Cantliffe
Daniel J. Cantliffe
Among Cucurbitaceae, Cucumis melo is one of the most important cultivated cucurbits. They are grown primarily for their fruit, which generally have a sweet aromatic flavor, with great diversity and size (50 g to 15 kg), flesh color (orange, green, white, and pink), rind color (green, yellow, white, orange, red, and gray), form (round, flat, and elongated), and dimension (4 to 200 cm). C. melo can be broken down into seven distinct types based on the previously discussed variations in the species. The melon fruits can be either climacteric or nonclimacteric, and as such, fruit can adhere to the stem or have an abscission layer where they will fall from the plant naturally at maturity. Traditional plant breeding of melons has been done for 100 years wherein plants were primarily developed as open-pollinated cultivars. More recently, in the past 30 years, melon improvement has been done by more traditional hybridization techniques. An improvement in germplasm is relatively slow and is limited by a restricted gene pool. Strong sexual incompatibility at the interspecific and intergeneric levels has restricted rapid development of new cultivars with high levels of disease resistance, insect resistance, flavor, and sweetness. In order to increase the rate and diversity of new traits in melon it would be advantageous to introduce new genes needed to enhance both melon productivity and melon fruit quality. This requires plant tissue and plant transformation techniques to introduce new or foreign genes into C. melo germplasm. In order to achieve a successful commercial application from biotechnology, a competent plant regeneration system of in vitro cultures for melon is required. More than 40 in vitro melon regeneration programs have been reported; however, regeneration of the various melon types has been highly variable and in some cases impossible. The reasons for this are still unknown, but this plays a heavy negative role on trying to use plant transformation technology to improve melon germplasm. In vitro manipulation of melon is difficult; genotypic responses to the culture method (i.e., organogenesis, somatic embryogenesis, etc.) as well as conditions for environmental and hormonal requirements for plant growth and regeneration continue to be poorly understood for developing simple in vitro procedures to culture and transform all C. melo genotypes. In many cases, this has to be done on an individual line basis. The present paper describes the various research findings related to successful approaches to plant regeneration and transgenic transformation of C. melo. It also describes potential improvement of melon to improve fruit quality characteristics and postharvest handling. Despite more than 140 transgenic melon field trials in the United States in 1996, there are still no commercial transgenic melon cultivars on the market. This may be a combination of technical or performance factors, intellectual property rights concerns, and, most likely, a lack of public acceptance. Regardless, the future for improvement of melon germplasm is bright when considering the knowledge base for both techniques and gene pools potentially useable for melon improvement.

1 March 2013 in Biologia plantarum
Verified
Journal Article
Closed access
PDF file
CAC. Aza-González
C. Aza-González
LHL. Herrera-Isidrón
L. Herrera-Isidrón
Hector Nuñez-PaleniusHector Nuñez-Palenius
Hector Nuñez-Palenius
Octavio MartínezOctavio Martínez
Octavio Martínez
NONeftalí Ochoa-Alejo
Neftalí Ochoa-Alejo
Chili pepper (Capsicum annuum L.) cv. ?rbol and Uvilla fruits differing in anthocyanin contents were analyzed to characterize the accumulation patterns. The maximum accumulation of the aglycon delphinidin occurred 20 days postanthesis (DPA) wi...

16 December 2005 in Plant Cell Reports
Verified
Journal Article
Closed access
PDF file
Hector Nuñez-PaleniusHector Nuñez-Palenius
Hector Nuñez-Palenius
DCDaniel J. Cantliffe
Daniel J. Cantliffe
DHDon J. Huber
Don J. Huber
JCJoseph Ciardi
Joseph Ciardi
HKHarry J. Klee
Harry J. Klee

1 November 2005 in In Vitro Cellular & Developmental Biology - Plant
Verified
Journal Article
Closed access
PDF file
Hector Nuñez-PaleniusHector Nuñez-Palenius
Hector Nuñez-Palenius
NONeftalí Ochoa-Alejo
Neftalí Ochoa-Alejo
Chili pepper (Capsicum annuum L., cv. Tampiqueño 74) cell suspensions were employed to study the influence of phenylalanine and phenylpropanoids on the total production of capsaicinoids, the hot taste compounds of chili pepper fruits. The effect of capsaicinoid precursors and intermediates on the accumulation of lignin as an indicator of metabolic diversion was also investigated. Addition of 100 μM of either phenylalanine, cinnamic or caffeic acids to chili pepper cell cultures did not cause significant increases in total capsaicinoids (expressed as capsaicin content, and calculated as averages of the measured values) during the growth cycle. The highest total capsaicinoid content was recorded in cultures grown in the presence of vanillin (142.61 μg g−1 f.wt.), followed by cells treated with 100 μM vanillylamine (104.88 μg g−1 f.wt.), p-coumaric acid (72.36 μg g−1 f.wt.). and ferulic acid (34.67 μg g−1 f.wt.). Capsaicinoid content for control cells was 13.97 μg g−1 f.wt. Chili pepper cell suspensions cultured in the presence of 100 μM of either phenylalanine, or cinnamic, caffeic, or ferulic acids, or the same concentration, of vanillin and vanillylamine, did not exhibit statistically significant differences in the content of lignin as compared with control cells. However, addition of p-coumaric acid (100 μM) to the cultute medium significantly increased thelignin production (c. 10–15 times the contents of control cells).

6 January 2023 in Horticulturae
Verified
Journal Article
Open access
PDF file
YJYamir Jiménez-Viveros
Yamir Jiménez-Viveros
Hector Nuñez-PaleniusHector Nuñez-Palenius
Hector Nuñez-Palenius
GRGrisel Fierros Romero
Grisel Fierros Romero
Juan Valiente-BanuetJuan Valiente-Banuet
Juan Valiente-Banuet
Capsicum is one of the most economically important genera in the Solanaceae family. Capsicum fruits (peppers) are rich in phytochemicals with high nutritional value and significant health-promoting characteristics. The phytochemical profile of peppers consists of capsaicinoids, carotenoids, and phenolics, primarily. Currently, most of the pepper production is carried out under protected horticulture conditions. The objective of this article was to provide a comprehensive review on how light characteristics and manipulation by different horticultural technologies can affect the biosynthesis and accumulation of phytochemicals in Capsicum fruits. The use of shade nets or plastic covers to reduce light intensity does not seem to yield consistent responses on the phytochemical profile, as the final profile results from the interaction of several factors. Other factors involved in the accumulation of phytochemicals include temperature, water availability and plant nutrition. Exposure of plants to supplemental light with specific wavelengths (using LEDs) seems to result in a more precise stimulation of specific metabolites. In this article, we examine the effects of light irradiance and spectrum on the specific phytochemicals of Capsicum fruits.