Studies on Bacterial Cell Multiplication

Chemical composition of the filamentous cells of Lactobacillus delbrueckii produced by vitamin B₁₂ deficient culture was studied. Protein and RNA contents per unit cell volume of the filamentous cells were nearly equal to those of normal cells, but the DNA content was much reduced. A cytoplast of the filamentous cell possessed about twice as large volume as that of the normal cell. A cytoplast of either filamentous or normal cell seems to contain the same amount of DNA. DNA level and membrane formation necessary for cell division remained as future problems.     

Multiplication of Listeria in milk products

The results of the evaluation of the multiplication dynamics of Listeria cells in milk and Bifidok, a lactic acid product, are presented. The samples were inoculated on thioglycol agar and studied at different exposure time after incubation at 37 degrees C, 20 degrees C and 4 degrees C. The study revealed the intensive multiplication of Listeria cells in milk, also during storage in a household refrigerator. The presence of bifidobacteria mixed with kefir-producing culture in dairy products was shown to essentially inhibit the growth of Listeria cells which were not detected by bacteriological techniques on day 7.     

Multiplication of a restriction-modification gene complex

Previous works have suggested that some gene complexes encoding a restriction (R) enzyme and a cognate modification (M) enzyme may behave as selfish mobile genetic elements. RM gene complexes, which destroy 'non-self' elements marked by the absence of proper methylation, are often associated with mobile genetic elements and are involved in various genome rearrangements. Here, we found amplification of a restriction-modification gene complex. BamHI gene complex inserted into the Bacillus chromosome showed resistance to replacement by a homologous stretch of DNA. Some cells became transformed with the donor without losing BamHI. In most of these transformants, multiple copies of BamHI and the donor allele were arranged as tandem repeats. When a clone carrying one copy of each allele was propagated, extensive amplification of BamHI and the donor unit was observed in a manner dependent on restriction enzyme gene. This suggests that restriction cutting of the genome participates in the amplification. Visualization by fluorescent in situ hybridization revealed that the amplification occurred in single cells in a burst-like fashion that is reminiscent of induction of provirus replication. The multiplication ability in a bacterium with natural capacity for DNA release, uptake and transformation will be discussed in relation to spreading of RM gene -complexes.     

Operational Momentum in Multiplication and Division?

Biases are commonly seen in numerical cognition. The operational momentum (OM) effect shows that responses to addition and subtraction problems are biased in the whole-number direction of the operation. It is not known if this bias exists for other arithmetic operations. To determine whether OM exists in scalar operations, we measured response bias in adults performing symbolic (Arabic digits) and non-symbolic (dots) multiplication and division problems. After seeing two operands, with either a multiplication (×) or division (÷) sign, participants chose among five response choices. Both non-random performance profiles and the significant contribution of both operands in a multiple regression analysis predicting the chosen values, suggest that adults were able to use numerical information to approximate the outcomes in both notations, though they were more accurate on symbolic problems. Performance on non-symbolic problems was influenced by the size of the correct choice relative to alternatives. Reminiscent of the bias in addition and subtraction, we found a significant response bias for non-symbolic problems. Non-symbolic multiplication problems were overestimated and division problems were underestimated. These results indicate that operational momentum is present in non-symbolic multiplication and division. Given the influence of the size of the correct choice relative to alternatives, an interaction between heuristic bias and approximate calculation is possible.     

Multiplication of juvenile black wattle by microcuttings

The influence of mineral formulation, growth regulators and activated charcoal on micropropagation of juvenile black wattle (Acacia mearnsii) was studied. Nodal segments of one-month-old seedlings were used as starting material. After 30 to 45 days, they developed into shoots, which were divided into microcuttings and transferred to fresh media. The addition of 2 g l⁻¹ of activated charcoal to basal medium (3/4 strength MS salts and MS vitamins) improved the multiplication phase, reducing leaf chlorosis and raising the percentage of elongated shoots. The multiplication rate varied between 1.7 and 3 every month. Rooting percentage too was higher in the presence of charcoal, even when auxin was not added to the culture medium. The addition of 8.87 μM of benzyladenine and/or 1.44 or 2.88 μM of gibberellic acid did not influence significantly the multiplication, nor modifications in the FeSO₄, MnSO₄, CaCl₂ content of the medium. The system described allows the multiplication, elongation and rooting of black wattle in one step. This revised version was published online in June 2006 with corrections to the Cover Date.     

Rapid In Vitro Multiplication of Dalbergia sissoo Roxb

Micropropagation of Dalbergia sissoo Roxb was achieved through in vitro proliferation of axillary buds from 30 to 40 years old mature tree. Bud-break was achieved within six days when nodal explants were cultured on MS medium supplemented with kinetin (9.2 μm), indole-3-butyric acid (2.46 μM) apd 6-benzyladenine (13.2 μM). Multiple shoot formation occurred from nodal explants of in vitro raised shoots on MS medium with reduced levels of major salts and kinetin. Roots were Induced within 5 days on in vitro generated shoots on MS medium supplemented with 1-naphthalene acetic acid (0.53 μM) and indole-3-butyric acid (9.8 μM).