Janos Pauk

Dr. Janos Pauk


Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

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

Representative Publications

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12 April 2009 in Plant Cell, Tissue and Organ Culture (PCTOC)
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CLCsaba Lantos
Csaba Lantos
AJAnikó Gémes Juhász
Anikó Gémes Juhász
GSGyörgy Somogyi
György Somogyi
KÖKrisztina Ötvös
Krisztina Ötvös
PVPál Vági
Pál Vági
JPJanos Pauk
Janos Pauk

21 November 2013 in Euphytica
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CLCsaba Lantos
Csaba Lantos
LBLajos Bóna
Lajos Bóna
BKBoda Krisztina
Boda Krisztina
JPJanos Pauk
Janos Pauk

9 December 2022 in Plants
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CLCsaba Lantos
Csaba Lantos
MJMihaly Jancso
Mihaly Jancso
ÁSÁrpád Székely
Árpád Székely
ÉNÉva Nagy
Éva Nagy
TSTímea Szalóki
Tímea Szalóki
JPJanos Pauk
Janos Pauk
Doubled haploid (DH) plant production, such as anther culture (AC), is an effective tool used in modern rice breeding programs. The improved efficient protocols applied can shorten the process of breeding. The effect of combinations of plant growth regulators (2.5 mg/L NAA, 1 mg/L 2,4-D and 0.5 mg/L kinetin; 2 mg/L 2,4-D and 0.5 mg/L BAP) in the induction medium were compared in AC for five rice breeding materials and combinations. Induction of calli ranged from 264.6 ± 67.07 to 468.8 ± 123.2 calli/100 anthers in AC of rice genotypes. Two basal media (MS and N6) and two combinations of growth regulators (1 mg/L NAA, 1 mg/L BAP and 1 mg/L kinetin; 1.5 mg/L BAP, 0.5 mg/L NAA and 0.5 mg/L kinetin) were used as regeneration media. The in vitro green plant production was the highest with the application of the N6NDK induction medium (NAA, 2,4-D and kinetin) and the MS-based regeneration medium (1 mg/L NAA, 1 mg/BAP and 1 mg/L kinetin) in anther culture of the ‘1009’ genotype (95.2 green plantlets/100 anthers). The mean of five genotypes was 24.48 green plantlets/100 anthers for the best treatment. Flow cytometric analyses conducted identified the microspore origin of the haploid calli produced in AC, while the uniformity of spontaneous DH plants was checked in the DH1 and DH2 generations. Spontaneous chromosome doubling ranged from 38.1% to 57.9% (mean 42.1%), depending on the breeding source. The generated and selected DH lines were tested in micro- and small-plot field experiments to identify promising lines for a pedigree breeding program. The improved AC method was integrated in a Hungarian temperate rice pedigree breeding program.

1 August 2016 in Russian Journal of Genetics
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CLC. Lantos
C. Lantos
JPJanos Pauk
Janos Pauk

22 October 2019 in Plants
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CLCsaba Lantos
Csaba Lantos
SPSzandra Purgel
Szandra Purgel
KÁKatalin Ács
Katalin Ács
BLBernadett Langó
Bernadett Langó
LBLajos Bóna
Lajos Bóna
JPJanos Pauk
Janos Pauk
The efficiency of in vitro anther culture was screened in a full diallel population of four spelt wheat genotypes and ten F1 hybrids. Genotype dependency was observed based on the data of embryo-like structures (ELS), green-, albino plantlets. In the diallel population and ten F1 hybrids, the green plantlets production ranged from 13.75 to 85.00 and from 6.30 to 51.00, respectively. The anther culture-derived plants of F1 hybrids were grown up in the nursery. At the harvest, 436 spontaneous doubled haploid (DH) plants were identified among the 1535 anther culture-derived transplanted and grown up individual plants. The mean of spontaneous rediploidization was 28.4% which ranged from 9.76% to 54.24%. In two consecutive years, the agronomic values of ‘Tonkoly.pop1’ advanced line were compared with seven DH lines of ‘Tonkoly.pop1’ in the nursery. The DH lines achieved competitive values in comparison with ‘Tonkoly.pop1’ advanced line based on the 11 measured parameters (heading date, plant height, yield, hardness, width and length of seed, TKW, hulling yield, flour yield, protein and wet gluten content). These observations presage the efficient utilization of anther culture in spelt wheat breeding.

28 February 2018 in Plant Cell, Tissue and Organ Culture (PCTOC)
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Journal Article
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CLCsaba Lantos
Csaba Lantos
LBLajos Bóna
Lajos Bóna
ÉNÉva Nagy
Éva Nagy
FBFerenc Békés
Ferenc Békés
JPJanos Pauk
Janos Pauk