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Acta Prataculturae Sinica ›› 2026, Vol. 35 ›› Issue (10): 156-166.DOI: 10.11686/cyxb2025434

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Optimization of an embryonic callus induction and subculture system for Zoysia japonica cv. ‘Zenith’

Ci REN1(), Yi-hua WANG1, Long-long MA1, Cui-ling LIU1, Jie-yi LI1, Chao LIU1, Liang-liang HE1, Shu CHEN1,2,3()   

  1. 1.College of Forestry and Landscape Architecture,South China Agricultural University,Guangzhou 510642,China
    2.Guangdong Engineering Research Center for Grassland Science,Guangzhou 510642,China
    3.South China Agricultural University Zhongshan Innovation Center,Zhongshan 528478,China
  • Received:2025-10-21 Revised:2025-12-15 Online:2026-10-20 Published:2026-09-09
  • Contact: Shu CHEN

Abstract:

There are several technical bottlenecks in Zoysia japonica tissue culture, including the low induction rate of embryogenic callus and severe browning during subculture. This study aimed to address these problems to establish an efficient and stable plant regeneration system for Z. japonica. Mature seeds of the seed-propagated cultivar ‘Zenith’ were used as explants. These explants were cultured on basal induction medium (IM) consisting of Murashige & Skoog medium supplemented with 2 mg·L-1 2,4-dichlorophenoxyacetic acid and 0.2 mg·L-1 6-benzylaminopurine. Key regulatory factors were screened through three successive rounds of single-factor experiments. The first round of screening revealed a promoting effect of 5 mg·L-1 vitamin B1 and 25 mg·L-1 α-ketoglutaric acid on embryogenic callus induction, although the maximum embryogenic callus induction rate was only 6.74%. The second round of screening identified dicamba (2 mg·L-1) as a core hormonal regulator that significantly increased the embryogenic callus induction rate to 19.65%. In the third round of screening, the addition of 25 mg·L-1 α-ketoglutaric acid to IM+2 mg·L-1 dicamba further increased the embryogenic callus induction efficiency by 62.38%. The addition of 0.05 mg·L-1 abscisic acid to the medium effectively inhibited premature differentiation of callus during subculturing. Browning was significantly suppressed by the addition of 4 g·L-1 polyvinylpyrrolidone (PVP), 0.5-1.0 g·L-1 activated carbon, or 0.001-0.005 g·L-1 silver nitrate, with PVP demonstrating the strongest inhibitory effect. In summary, a complete, efficient regeneration system was established for Z. japonica. This system provides a reliable source of recipient materials for molecular breeding applications such as gene editing and genetic transformation. The findings of this study provide a valuable theoretical and technical reference for developing regeneration systems for other warm-season turf grasses.

Key words: Zoysia grass, tissue culture, callus, regeneration system