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. 2019 Sep 25;36(3):181–185. doi: 10.5511/plantbiotechnology.19.0814a

Figure 4. Survey of rhizosphere microbial population. (A–D) Rhizosphere microbes of transgenic and non-transgenic Oncidium orchids were cultivated by OGYE plate cultivation for fungi (A and B) and PTYG plate cultivation for bacteria including actinomycetes (C and D). (E–G) Calculated colony-forming units of fungi, actinomycetes, and bacteria were shown in E, F and G, respectively. The error bars indicate standard error. Five individuals of each orchid were used repeatedly. ANOVA did not show any significant difference between the transgenic and non-transgenic orchids (E–G). HA, Oncidium “Honey Angel”; MF-1, Oncidium “Honey Snow” MF-1. There were no significant differences between the transgenic and non-transgenic Oncidium orchids by ANOVA (p>0.05).

Figure 4. Survey of rhizosphere microbial population. (A–D) Rhizosphere microbes of transgenic and non-transgenic Oncidium orchids were cultivated by OGYE plate cultivation for fungi (A and B) and PTYG plate cultivation for bacteria including actinomycetes (C and D). (E–G) Calculated colony-forming units of fungi, actinomycetes, and bacteria were shown in E, F and G, respectively. The error bars indicate standard error. Five individuals of each orchid were used repeatedly. ANOVA did not show any significant difference between the transgenic and non-transgenic orchids (E–G). HA, Oncidium “Honey Angel”; MF-1, Oncidium “Honey Snow” MF-1. There were no significant differences between the transgenic and non-transgenic Oncidium orchids by ANOVA (p>0.05).