Minnich S A, Aronson A I
J Bacteriol. 1984 May;158(2):447-54. doi: 10.1128/jb.158.2.447-454.1984.
A derivative of Bacillus thuringiensis subsp. kurstaki (HD-1) formed parasporal inclusions at 25 degrees C, but not at 32 degrees C. This strain differed from the parent only in the loss of a 110-megadalton (Md) plasmid, but plasmid and chromosomal copies of protoxin genes were present in both strains. On the basis of temperature shift experiments, the sensitive period appeared to be during midexponential growth, long before the time of protoxin synthesis at 3 to 4 h after the end of exponential growth. The conditional phenotype could be transferred by cell mating to naturally acrystalliferous Bacillus cereus. In all such cases, a 29-Md protoxin -encoding plasmid was transferred, but this plasmid alone was barely sufficient for protoxin synthesis. Protoxin production increased to detectable levels, but well below those of the parental donor strain, by simultaneous transfer of a 44-Md protoxin -encoding plasmid. Transfer of a 5-Md plasmid with the two larger protoxin -coding plasmids resulted in a protoxin synthesis level approaching that of the donor strain. A role for some of the cryptic plasmids of kurstaki in parasporal body formation was implied. In contrast, a closely related B. thuringiensis strain, HD73 , produced crystals at both 25 and 32 degrees C even when the capacity was transferred on a 50-Md plasmid to B. cereus. The amount of protoxin produced in these B. cereus transcipients , however, was somewhat less than that produced in the parental strain HD73 , implying that catabolic differences, gene dosage, or the presence of a chromosomal gene (or a combination of these) may be necessary for maximum production. A regulatory component of the 29-Md plasmid appeared to be trans-acting and dominant since B. cereus transcipients containing the 29-Md plasmid from kurstaki and the 50-Md plasmid from HD73 produced more protoxin at 25 degrees C than at 30 degrees C. Similar results were obtained when protoxin synthetic capacity was transferred from B. thuringiensis subsp. israelensis to the conditional B. thuringiensis subsp. kurstaki strain.
苏云金芽孢杆菌库斯塔克亚种(HD - 1)的一个衍生物在25℃时形成伴孢晶体,而在32℃时不形成。该菌株与亲本的区别仅在于丢失了一个110兆道尔顿(Md)的质粒,但两种菌株中都存在原毒素基因的质粒和染色体拷贝。根据温度转换实验,敏感期似乎是在指数生长中期,远早于指数生长结束后3至4小时原毒素合成的时间。这种条件表型可以通过细胞交配转移到天然无晶体的蜡状芽孢杆菌中。在所有这些情况下,一个29 - Md的原毒素编码质粒被转移,但仅这个质粒几乎不足以进行原毒素合成。通过同时转移一个44 - Md的原毒素编码质粒,原毒素产量增加到可检测水平,但远低于亲本供体菌株的水平。将一个5 - Md质粒与两个较大的原毒素编码质粒一起转移,导致原毒素合成水平接近供体菌株。这暗示了库斯塔克亚种的一些隐蔽质粒在伴孢体形成中起作用。相比之下,一个密切相关的苏云金芽孢杆菌菌株HD73,即使其形成晶体的能力通过一个50 - Md的质粒转移到蜡状芽孢杆菌中,在25℃和32℃时都能产生晶体。然而,这些蜡状芽孢杆菌转导子中产生的原毒素量比亲本菌株HD73中产生的略少,这意味着分解代谢差异、基因剂量或染色体基因的存在(或这些因素的组合)可能是最大产量所必需的。29 - Md质粒的一个调控成分似乎是反式作用且占主导地位的,因为含有来自库斯塔克亚种的29 - Md质粒和来自HD73的50 - Md质粒的蜡状芽孢杆菌转导子在25℃时比在30℃时产生更多的原毒素。当原毒素合成能力从苏云金芽孢杆菌以色列亚种转移到条件性的苏云金芽孢杆菌库斯塔克亚种菌株时,也获得了类似的结果。