The use of biotechnology for genetic improvement of bamboo is one of the researches of bamboo breeding. And the basic research of bamboo genetic improvement breeding is to build a stable bamboo regeneration system. Bambusa ventricosa McClure is a graceful bamboo for view. This research focused on the buds proliferation and plant regeneration, callus culture. The results are as follows:1. The buds proliferation and plant regeneration of Bambusa ventricosa McClure(1) The best conditions for stalk bud germinating was:explant soaked by 70% alcohol 30s, used 0.1% HgCl2, disinfected 5minutes, MS basic medium,6-BA 5mg/L.(2) The suitable medium for buds induction was MS+6-BA 6mg/L+NAA 0.2mg/L+sucrose 30g/L+agar 6.5g/L.(3) The fessible medium for buds proliferation was MS+6-BA 5mg/L+TDZ 0.05mg/L +NAA 0.2mg/L+sucrose 30g/L+agar 6.5g/L.(4) The optimizing medium for regenerated plantlet rooting was MS+NAA 0.5mg/L+IBA 0.1mg/L+6-BA lmg/L+sucrose 30g/L+agar 6.5g/L.(5) The regenerated Plantlet transplanting was perlite:vermiculite:loam(1:1:1). 2. Callus culture of Bambusa ventricosa McClure(1) The best preparation conditions for callus culture was sucrose 30g/L, Vc100mg/L, sterile stem segments as explants is the most appropriate choice.(2) The fessible medium for callus induction was MS+2,4-D 4mg/L+6-BA 0.5mg/L+sucrose 30g/L+agar 6.5g/L.TypeⅠ:Pale white to light yellow, compact structure, granular, hard texture of the embryogenic callus which can be used to further proliferation and differentiation of experimental.TypeⅡ:light brown, water damaged seriously, scattered in the tight or loose friable callus, and such kind of callus is vulnerable to browning.TypeⅢ:White or translucent, loose, friable non-embryogenic callus.(3) The suitable medium for callus proliferation was:MS+2,4-D 3mg/L+NAA 0.5mg/L +6-BA 0.1mg/L+sucrose 30g/L+agar 6.5g/L. |