TAP培养基-莱茵衣藻

tap培养基用于莱茵衣藻的培养,以下为原版配方

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.

TAP 培养基

 

Related Posts

Read More

Basal Medium Eagle

BME培养基产品基本信息 产品名称: BME培养基 英文名称: Basal Medium Eagle;BME 培养基类型: 哺乳动物细胞培养基 级别: cell culture tested 品牌: ELITE-MEDIA 产品目录号:…

Walne’s 培养基 (Walne’s medium)

Walnes 培养基 (Walnes medium)是一种国外常用的海水藻类培养基,光语生物提供商品装培养基,客户也可以根据如下配方配置。 Walne’s Medium Composition From https://biocyclopedia.com/index/algae/algal_culturing/walnes_medium_composition.php Reagents Per L […]…

光合细菌培养基 Read More

光合细菌培养基好用吗?

  光合细菌培养基好用吗?如何使用光语公司的光合细菌培养基?   光合细菌在水产养殖中的运用非常广泛,是净水、调水的小能手。光合细菌可以降解水体中的有机物,如鱼虾残饵、粪便等,可以吸收水中的有害物质,如氨氮、亚硝酸盐、硫化氢等。水产养殖中长期使用光合细菌,可以有效避免有害物质沉积,减少鱼虾生病的机率,提高鱼虾产量。   现在我们来介绍下,养殖户如何自己培育光合细菌?   养殖户自己培育光合细菌不仅 […]…

Write a comment