I used leaf explant and inoculated onto solid MS media after 4 weeks of incubation i transferred it into liquid media, after 3 days of incubation the media turned turbid and i could see round white mass of fungi.
The reason is that you have some (1-2) fungi spores in your tissue (explant surface), which start to growth in the liquid. There are almost no way to remove fungi, except restarelization of addion of some preservatives (look on companies web-site). There are no antibiotics against fungi...
The reason is that you have some (1-2) fungi spores in your tissue (explant surface), which start to growth in the liquid. There are almost no way to remove fungi, except restarelization of addion of some preservatives (look on companies web-site). There are no antibiotics against fungi...
I agreed with Mr. Pedro, this contamination coming from explants source, and during this stage its very difficult to remove it. I faced many problems like this situation. and you can reduce it by:
1- Rinse explant by fungicide for 12-24 hours before inoculation onto solid media.
2- add antibiotic such as tetracycline to your media
the explant leaf may not contain the fungal spore which germinated into the mycelium.
This is because the explant was in culture for 4 months free of fungal growth. Fungi or bacteria develop quickly in in vitro ocnditions with in 2/3 days.
Your 2nd medium-liquid medium must had the fungal spore which resulted in the mycelial growth, in which case the medium was not properly autoclaved. Or during the subculture, the fungal spore must have got into the medium.
Fungal growth can be controlled by the fungicide Bavistin. Some times, when we know the explant is collected from a humid environment, we add Bavistin
( eg,0.1mg/ml) to the medium before the medium is autoclaved.
But Bavistin will also have affect on explant/callus/regenerants.
Thank you for your question. In my opinion the culture having some fungal spore and it will grow very faster in liquid medium. In some cases, some endophytic fungus or bacteria will create problem in liquid medium. Before you state experiment, you may filtrate your liquid medium through 0.45 uM sterile microfilter. But if you are culturing in either liquid medium or semisolid medium you may use carbenicillin. (50 mg/l) to check the fungal infection.
The culture may be having some fungal spore. It will grow very faster in liquid medium. In some cases, some endophytic fungus or bacteria will create problem in liquid medium. Before you state experiment, you may filtrate your liquid medium through 0.45 uM sterile microfilter. But if you are culturing in either liquid medium or semisolid medium you may use carbenicillin. (50 mg/l) to check the fungal infection.
It might be possible that some fungal spores might be present on your explant which is creating problem of contamination. To avoid such contamination you should modify the protocol of surface sterilization of explant by using multiple wash of fungicides.
It is also possible that there might be fungal contamination in the liquid medium due to improper sterilization. There are some articles regarding use of fungicides in plant tissue culture media. So you may add some fungicides with antibiotics in the medium to prevent contamination. However it may reduce the growth of the explant which depends on the fungicide you use and plant species of which the explant is.
this may be an endophyte. if this is the case then you have to find out another explant source. sometimes endophytes will make their appearance on transferring to the liquid medium.
It might be due to the fungal spores on the explant. Before inoculating, u can surface sterilise using sodium hypochlorite and HgCl2. U can also use antifungal agents in the liquid media