Beuchat L R, Lechowich R V
Appl Microbiol. 1971 Jan;21(1):119-23. doi: 10.1128/am.21.1.119-123.1971.
Bacillus megaterium NRRL B-1368 cells and spores were produced on Trypticase Soy Broth (TSB) and Agar (TSA) containing 3.8 mug of aflatoxin B(1) per ml, analyzed for selected chemical constituents, and compared to cells and spores of B. megaterium produced on nontoxic Trypticase Soy Media. There was an initial 30% kill of cells after inoculation into toxic TSB and during the first 3.5 hr of incubation followed by a logarithmic growth phase in which the generation time was 75 min as compared to 20 min for the control culture. Chemical analyses revealed an increase in protein, deoxyribonucleic acid (DNA), and ribonucleic acid (RNA) on both a per cell basis and a per cent dry weight basis when B. megaterium was grown in toxic TSB. There was a concurrent decrease in the total amounts of cellular protein, DNA, and RNA synthesized in toxic TSB. Amino acid analyses of control and test cell walls showed little, if any, difference in cell wall composition. About 97% sporulation of B. megaterium occurred after 3 days on nontoxic TSA although 6 days were required to attain 65% sporulation on toxic TSA. Germination of spores was not inhibited by 4.0 mug of aflatoxin per ml but outgrowth was. No significant differences were observed in the heat resistance, protein, DNA, RNA, or dipicolinic acid content of spores formed on toxic TSA and nontoxic TSA.
巨大芽孢杆菌NRRL B - 1368的细胞和孢子在每毫升含有3.8微克黄曲霉毒素B(1)的胰蛋白胨大豆肉汤(TSB)和琼脂(TSA)上产生,对其选定的化学成分进行分析,并与在无毒胰蛋白胨大豆培养基上产生的巨大芽孢杆菌的细胞和孢子进行比较。接种到有毒TSB后,最初30%的细胞被杀死,在培养的前3.5小时内,随后进入对数生长期,其代时为75分钟,而对照培养物的代时为20分钟。化学分析表明,当巨大芽孢杆菌在有毒TSB中生长时,基于每个细胞和基于干重百分比计算,蛋白质、脱氧核糖核酸(DNA)和核糖核酸(RNA)均增加。在有毒TSB中合成的细胞蛋白质、DNA和RNA的总量同时减少。对照和测试细胞壁的氨基酸分析表明,细胞壁组成几乎没有差异(如果有差异也是极小的)。在无毒TSA上培养3天后,巨大芽孢杆菌约97%形成孢子,而在有毒TSA上则需要6天才能达到65%的孢子形成率。每毫升4.0微克的黄曲霉毒素不会抑制孢子的萌发,但会抑制其生长。在有毒TSA和无毒TSA上形成的孢子的耐热性、蛋白质、DNA、RNA或吡啶二羧酸含量未观察到显著差异。