24小时热门版块排行榜    

查看: 3225  |  回复: 16
当前只显示满足指定条件的回帖,点击这里查看本话题的所有回帖

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.
回复此楼
已阅   回复此楼   关注TA 给TA发消息 送TA红花 TA的回帖

superzbobo

木虫 (初入文坛)

引用回帖:
10楼: Originally posted by huoxinglizi at 2014-10-29 17:06:21
TAP培养基营养丰富,非常容易染菌。一旦染菌,藻的脱菌处理很麻烦,且耽误时间。建议培养基配好一定要灭菌。
根据本人的经验,浑浊是染菌表现。单纯的浑浊为细菌,絮状为霉菌

嗯,是的,确实是染菌了。
现在没问题了
11楼2014-10-29 18:39:46
已阅   回复此楼   关注TA 给TA发消息 送TA红花 TA的回帖
查看全部 17 个回答

superzbobo(金币+2): 谢谢参与
祝福

[ 发自小木虫客户端 ]
4楼2014-08-10 19:35:02
已阅   回复此楼   关注TA 给TA发消息 送TA红花 TA的回帖

superzbobo

木虫 (初入文坛)

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
已阅   回复此楼   关注TA 给TA发消息 送TA红花 TA的回帖

Micah1011

银虫 (小有名气)

【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

[ 发自小木虫客户端 ]
每天叫醒我的不是闹钟,是梦想;每天让我做实验的不是老板,是兴趣
7楼2014-08-11 08:10:51
已阅   回复此楼   关注TA 给TA发消息 送TA红花 TA的回帖
最具人气热帖推荐 [查看全部] 作者 回/看 最后发表
[基金申请] 投票:  有多少人是今天查系统知道结果的? +17 爱看书的可乐 2026-08-26 19/950 2026-08-30 22:24 by xiangy672
[基金申请] 能否申诉? +4 echo8914667 2026-08-30 5/250 2026-08-30 21:11 by echo8914667
[基金申请] 为什么到现在没收到通知? +5 tannykie 2026-08-29 5/250 2026-08-30 21:05 by purplejack
[基金申请] 有没有仍没收到信息的 +7 德尚中行 2026-08-27 8/400 2026-08-30 20:52 by purplejack
[考博] 找导师 +6 yuanjiabao 2026-08-29 7/350 2026-08-30 14:40 by 生科新手
[基金申请] 29号明天会评吗 +3 笨笨唐 2026-08-28 3/150 2026-08-30 09:29 by cww8181
[基金申请] 我就是申请一个面上项目而已,这评审意见是按照杰青的条件评的吧? +6 gouxfjh 2026-08-28 11/550 2026-08-30 07:57 by gouxfjh
[基金申请] 中青基了要发朋友圈吗? +4 349506619 2026-08-28 4/200 2026-08-29 22:41 by alongwaytogo
[基金申请] 国自然评审意见 +13 wangmingqi 2026-08-28 19/950 2026-08-29 10:22 by Poppy1104
[基金申请] 系统查不到 +11 董八千 2026-08-26 11/550 2026-08-28 18:06 by Leogzhya
[基金申请] 基金系统什么内容也没有 30+4 winsaint 2026-08-27 9/450 2026-08-28 11:06 by maolC
[基金申请] 面上合作单位盖章 +5 ssyjh 2026-08-27 5/250 2026-08-27 20:50 by gdfollow
[基金申请] 我不理解! +15 Edward_pc 2026-08-26 23/1150 2026-08-26 20:34 by zzuzxg
[基金申请] 2026年8月25日国自然放榜前突然收到列入评审专家邮件,有关系吗? +25 木水思豆 2026-08-25 28/1400 2026-08-26 14:53 by draco1987
[基金申请] 为什么国自然不能直接公布 +4 bjdxyxy 2026-08-26 4/200 2026-08-26 13:12 by qingmu1201
[基金申请] 国际合作可查了,中了面上 (EPI+1)(金币+50) +18 Ldrop2023 2026-08-26 18/900 2026-08-26 11:15 by cmrandy
[基金申请] 今天务委会开完了,明天出结果吗 +19 angus9576 2026-08-25 23/1150 2026-08-26 10:03 by zp519
[基金申请] 国合现在查不到了吗? +10 chengyan1220 2026-08-24 20/1000 2026-08-26 08:57 by peasantsprig
[基金申请] 在坚冰还盖着北海的时候,我看到了怒放的梅花。 (金币+10) +6 ziyangfang 2026-08-25 9/450 2026-08-25 20:26 by huagongfeihu
[基金申请] 某些机构,以效率低为荣,以效率低作为存在感 +9 yuleib84 2026-08-25 10/500 2026-08-25 17:14 by alexon
信息提示
请填处理意见