Silver nanoparticles and plant growth regulators improved micropropagation of Anoectochilus roxburghii (Wall.) Lindl. via protocorm-like bodies

• A high-efficiency micropropagation protocol for A. roxburghii (Wall.) Lindl. was established. • The roles of AgNPs, PGRs, and organic additives across the stages of micropropagation. • The plantlets grew best and high kinsenoside content in the greenhouse. A high-frequency micropropagation protocol for Anoectochilus roxburghii (Wall.) Lindl. was developed via protocorm regeneration, induction and proliferation of protocorm-like bodies (PLBs), shoot regeneration, in vitro rooting, and acclimatization. Silver nanoparticles (AgNPs) were used for surface disinfection of floral-buds to regenerate protocorm which was divided into node, intercalary meristem, and internode to induce PLBs under the influence of plant growth regulators - PGRs (auxin and cytokinin), and silver nanoparticles (AgNPs). In addition, the effect of organic supplements (coconut water, potato starch and peptone) on PLB proliferation and shoot regeneration, and the influence of AgNPs on in vitro rooting, acclimatization, and kinsenoside accumulation were also evaluated. After 30 days, flower-bud explants regenerated protocorms a rate of 83.00% and 3.45 protocorms/explant on Schenk & Hildebrandt (SH) medium supplemented with 1.0 mg/L 6-Benzylaminopurine (BAP) or Thidiazuron (TDZ) only after 60 days. PLBs were induced predominantly at the node–intercalary meristem junction from protocorms cultured on SH medium containing BAP, α-naphthaleneacetic acid (NAA), and 1.5 mg/L AgNPs. The highest PLB proliferation (50.33 PLBs/explant) and shoot regeneration (35 shoots/PLB cluster) were achieved on SH medium supplemented with 20% coconut water, 1.0 mg/L BAP, 0.5 mg/L NAA, and 1.5 mg/L AgNPs after 90 days. Plantlet growth (plantlet height, leaf number and width, root number and length, fresh/dry weight, and SPAD index – chlorophyll content) was maximal on SH medium with 2.0 mg/L AgNPs. Plantlets from media containing 2.0 g/L AgNPs were acclimatized in a peat moss: perlite (1:1) substrate and reached 85% survival after 12 months in the greenhouse. Kinsenoside contents increased with cultivation time (3, 6, 9, 12 months) peaking at 2.591% in the whole plant after 12 months. This study establishes an efficient micropropagation protocol for A. roxburghii via protocorm and PLB regeneration.

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Journal
South African Journal of Botany
Published
2026-02-24
DOI
https://doi.org/10.1016/j.sajb.2026.02.035
Primary Topic
Plant tissue culture and regeneration
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article
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article

Silver nanoparticles and plant growth regulators improved micropropagation of Anoectochilus roxburghii (Wall.) Lindl. via protocorm-like bodies

Hoàng Thanh Tùng, Phan Le Ha Nguyen, Dương Tấn Nhựt, Vũ Quốc Luận et al.
South African Journal of Botany
Plant tissue culture and regeneration
article

Silver nanoparticles and plant growth regulators improved micropropagation of Anoectochilus roxburghii (Wall.) Lindl. via protocorm-like bodies

Hoàng Thanh Tùng, Phan Le Ha Nguyen, Dương Tấn Nhựt, Vũ Quốc Luận, Trần Công Luận, Do Manh Cuong, Nguyen Thi Nhu Mai, Tran Thi Tam
article en

Abstract

• A high-efficiency micropropagation protocol for A. roxburghii (Wall.) Lindl. was established. • The roles of AgNPs, PGRs, and organic additives across the stages of micropropagation. • The plantlets grew best and high kinsenoside content in the greenhouse. A high-frequency micropropagation protocol for Anoectochilus roxburghii (Wall.) Lindl. was developed via protocorm regeneration, induction and proliferation of protocorm-like bodies (PLBs), shoot regeneration, in vitro rooting, and acclimatization. Silver nanoparticles (AgNPs) were used for surface disinfection of floral-buds to regenerate protocorm which was divided into node, intercalary meristem, and internode to induce PLBs under the influence of plant growth regulators - PGRs (auxin and cytokinin), and silver nanoparticles (AgNPs). In addition, the effect of organic supplements (coconut water, potato starch and peptone) on PLB proliferation and shoot regeneration, and the influence of AgNPs on in vitro rooting, acclimatization, and kinsenoside accumulation were also evaluated. After 30 days, flower-bud explants regenerated protocorms a rate of 83.00% and 3.45 protocorms/explant on Schenk & Hildebrandt (SH) medium supplemented with 1.0 mg/L 6-Benzylaminopurine (BAP) or Thidiazuron (TDZ) only after 60 days. PLBs were induced predominantly at the node–intercalary meristem junction from protocorms cultured on SH medium containing BAP, α-naphthaleneacetic acid (NAA), and 1.5 mg/L AgNPs. The highest PLB proliferation (50.33 PLBs/explant) and shoot regeneration (35 shoots/PLB cluster) were achieved on SH medium supplemented with 20% coconut water, 1.0 mg/L BAP, 0.5 mg/L NAA, and 1.5 mg/L AgNPs after 90 days. Plantlet growth (plantlet height, leaf number and width, root number and length, fresh/dry weight, and SPAD index – chlorophyll content) was maximal on SH medium with 2.0 mg/L AgNPs. Plantlets from media containing 2.0 g/L AgNPs were acclimatized in a peat moss: perlite (1:1) substrate and reached 85% survival after 12 months in the greenhouse. Kinsenoside contents increased with cultivation time (3, 6, 9, 12 months) peaking at 2.591% in the whole plant after 12 months. This study establishes an efficient micropropagation protocol for A. roxburghii via protocorm and PLB regeneration.

South African Journal of BotanyVol. 191
Can Tho University (VN), Dalat University (VN)
Openalex Percentile: Top 43%
Plant tissue culture and regeneration
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