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superzbobo

木虫 (初入文坛)

[求助] 衣藻 TAP培养基 已有3人参与

近来刚开始做藻类方面的实验。
用TAP培养基在培养衣藻,发现个很奇怪的问题,想向各位请教。
就是TAP培养基的问题,TAP培养基如果不灭菌,放在室温条件下,没一两天就浑浊了,有些小絮状沉淀的东西,镜检感觉不像染菌。
而灭菌的TAP培养基放室温条件下就不会,不知道可能是什么原因
因为另一个菌种用另一个培养基的话,即使不灭菌,在室温条件放着也不会浑浊呀
所以觉得TAP培养基有点奇怪  
非常感谢

附TAP培养基配方
TAP medium
from Gorman, D.S., and R.P. Levine (1965) Proc. Natl. Acad. Sci. USA 54, 1665-1669.
This is probably the most widely-used medium at present for experimental work.

Make the following stock solutions:
1. TAP salts

NH4Cl                 15.0 g
MgSO4 . 7H2O                 4.0 g
CaCl2 . 2H2O                 2.0 g
water to 1 liter                
2. phosphate solution

K2HPO4                 28.8 g
KH2PO4                 14.4 g
water to 100 ml                
3. Hutner's trace elements


To make the final medium, mix the following:
2.42 g Tris
25 ml solution #1 (salts)
0.375 ml solution #2 (phosphate)
1.0 ml solution #3 (trace elements)
1.0 ml glacial acetic acid
water to 1 liter
For solid medium, add 15 g agar per liter
Autoclave.
For Tris-minimal medium omit the acetic acid and titrate the final solution to pH 7.0 with HCl
Hutner's trace elements
Hutner et al. (1950) Proc. Am. Philos. Soc. 94, 152-170
This mixture is used both in TAP and in the Sueoka high salt medium.
For a detailed analysis of how well this trace elements solution meets the nutritional requirements of C. reinhardtii, see Merchant et al. (2006) Biochim. Biophys. Acta 1763, 578-594.

For 1 liter final mix, dissolve each compound in the volume of water indicated.

The EDTA should be dissolved in boiling water, and the FeSO4 should be prepared last to avoid oxidation.
compound        amount        water
EDTA disodium salt        50 g        250 ml
ZnSO4 . 7 H2O        22 g        100 ml
H3BO3        11.4 g        200 ml
MnCl2 . 4 H2O        5.06 g        50 ml
CoCl2. 6 H2O        1.61 g        50 ml
CuSO4 . 5 H2O        1.57 g        50 ml
(NH4)6Mo7O24. 4 H2O        1.10 g        50 ml
FeSO4. 7 H2O        4.99 g        50 ml
Mix all solutions except EDTA. Bring to boil, then add EDTA solution. The mixture should turn green. When everything is dissolved, cool to 70 degrees C. Keeping temperature at 70, add 85 ml hot 20% KOH solution (20 grams / 100 ml final volume). Do NOT use NaOH to adjust the pH.
Bring the final solution to 1 liter total volume. It should be clear green initially. Stopper the flask with a cotton plug and let it stand for 1-2 weeks, shaking it once a day. The solution should eventually turn purple and leave a rust-brown precipitate, which can be removed by filtering through two layers of Whatman#1 filter paper, repeating the filtration if necessary until the solution is clear. Store refrigerated or frozen convenient aliquots. Some people shorten the time for formation of the precipiate by bubbling the solution with filtered air.
If no precipitate forms, the solution is still usable. However, you might want to check the pH in this case and adjust it to around 7.0 using either KOH or HCl as needed.
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16楼2021-03-29 11:42:10
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superzbobo(金币+2): 谢谢参与
祝福

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4楼2014-08-10 19:35:02
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superzbobo

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有没有高手帮忙解答一下,TAP培养基浑浊是因为染菌了吗?显微镜下看不出来呀,还有什么其他可以确定染菌的方法吗
6楼2014-08-11 01:51:27
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Micah1011

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【答案】应助回帖

★ ★ ★ ★ ★
感谢参与,应助指数 +1
superzbobo: 金币+5, ★★★很有帮助 2014-08-11 15:32:44
引用回帖:
6楼: Originally posted by superzbobo at 2014-08-11 01:51:27
有没有高手帮忙解答一下,TAP培养基浑浊是因为染菌了吗?显微镜下看不出来呀,还有什么其他可以确定染菌的方法吗

取样,用营养琼脂划线,我觉得应该是染菌

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7楼2014-08-11 08:10:51
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