Origin and direction of replication of the drug resistance plasmid R100.1 and of a resistance transfer factor derivative in synchronized cultures.

The origin and direction of replication of the resistance plasmid R100.1 and its resistance transfer factor derivative, pAR132, were studied by electron microscopy autoradiography of partially denatured molecules and partial denaturation mapping of replicative intermediates. Results of these studies indicate the existence of an origin of replication at 8.8 kilobases on the R100 map. Replication from this origin in cultures synchronized for initiation of replication is predominantly unidirectional in a single direction.     

Suppression of an Escherichia coli dnaA mutation by the integrated R factor R100.1: generation of small plasmids after integration.

We have observed that integration of the R plasmid R100.1 into the chromosome of Escherichia coli is associated with the formation of small, covalently closed circular elements. Contour length measurements, partial denaturation mapping, and analysis of the deoxyribonucleic acid fragments produced by digestion of one of these, pLC1, with the restriction endonuclease EcoRI indicate that it is the r-determinant element of R100.1.     

Isolation of the kanamycin resistance region (Tn2350) of plasmid R1drd-19 as an autonomous replicon.

We have isolated a circular form of Tn2350, an IS1-flanked kanamycin resistance transposon forming part of the plasmid R1drd-19. This circle (pTn2350::9.6 kilobases) contains a single IS1 element and probably arises by recombination between the two directly repeated Is1 sequences of Tn2350. It can be used to transform Escherichia coli to kanamycin resistance. It is capable of autonomous replication but is not maintained stably in dividing cells and segregates under nonselective conditions. Cloning of a segment of pTn2350 on a conditional plasmid vector allowed us to assign the replication functions of this plasmid to a 1.6-kilobase restriction fragment. The plasmid R1drd-19 can thus be considered as a cointegrate between two replicons separated by IS1 sequences.     

The construction and replication properties of hybrid plasmids composed of the r-determinant of R100.1 and the plasmids pCRI or pSC201

Summary We have cloned the entire r-determinant of the antibiotic resistance plasmid R100.1 on the plasmid vectors pCR1 and pSC201. We find that the hybrid plasmids segregate from cultures in which replication of the vector is blocked. This suggests that the r-det is not capable of autonomous replication.     

Replication of prophage P1 during the cell cycle of Escherichia coli.

Summary We have followed, by DNA-DNA hybridization, the variation in the number of copies of prophage P1 relative to two chromosomal markers when the doubling time of the host cells is modified by a change in carbon source. The ratio of P1/chromosome terminus undergoes a twofold decrease when the cell doubling time increases from 24 to 215 min, whereas the ratio of P1/chromosome origin increases 1.4 fold; both ratios tend towards unity at slow growth rates. This suggests that the replication of prophage P1 is not simultaneous with chromosome initiation or chromosome termination. The chromosome replication time is unaffected by the presence of P1, and remains constant over the range of doubling times studied, with a value of about 40 min. Following amino acid starvation, the P1/chromosome origin ratio increases from 0.7 to 0.9, suggesting that P1 retains the ability to replicate after chromosome initiation has stopped and in the absence of essential amino acids. The results are discussed with reference to similar studies done on F and R1.     

The Fcu controlling-element system in maize

Summary The relationship between the Fcu controlling-element system and the spotted-dilute R system was investigated. The Fcu controlling-element system consists of the receptor element allele r-cu and the regulatory element Fcu. The equivalent components of the spotted-dilute R system are respectively R-r#2 (or R-r#2 Dil) and Spf. The R-r#2 allele of the latter system was shown to be responsive (mutable) to Fcu, provided that it has had an uninterrupted association with Dil or Dpf as evidenced by the color variegation of the aleurone tissue. The reverse test, in which the r-cu allele of the Fcu controlling element system was tested for its response to Spf, proved negative. This was surprising in view of the relationship and specificity between systems. The possibility was considered that maize controlling elements may have different sizes as is known for bacterial insertion sequences. —The variable dilute pigmenting capacity of the r-cu allele also was studied. A given level of r-cu-induced pigmentation, despite the wide range in pigmentation expression, was found to be generally non-heritable, as based on a test of correspondence between parent and progeny.Journal Paper No. J-9204 of the Iowa Agriculture and Home Economics Experiment Station, Ames, Iowa. Project No. 1884Now with Funk's Seeds, Casalmorano (Cremona), Italy     

Fitting multiple trajectories simultaneously to a model of inducible enzyme synthesis

The iterative scheme described by Milstein [6] is used to estimate the rate constants of a model describing an inducible enzyme system. The model was formulated by Heinmets [5], and was mathematically analyzed by Roth and Roth [9] using Bellman's quasilinearization technique. The method used in this article makes use of multiple trajectories of the system to obtain a set of parameters which fit the data of all trajectories simultaneously. A comparison of the numerical results is presented. The data used in the calculations were generated in a similar way to that of Roth and Roth. However, we introduce into each datum 5% noise from a random number generator uniformly distributed [0,1].     

β-Carotene, vitamin C and vitamin E content of the marine microalga Dunaliella tertiolecta cultured with different nitrogen sources

Variations in the β-carotene, vitamin C and vitamin E content of D. tertiolecta have been shown to result from the nitrogen source used in the culture medium. Differences of 101%, 38% and 69% have been found in β-carotene, ascorbic acid and tocopherol content in mg/g of dry matter, respectively, and differences of 147%, 63% and 37% occurred in β-carotene, vitamin C and E concentrations in mg/litre of culture, respectively. Considering the β-carotene, vitamin C and vitamin E content in mg/g of chlorophyll a, maximum variations occurred in β-carotene content, with differences of 145% among the different nitrogen sources. Maximum β-carotene and vitamin C values were found in urea cultures, whereas urea cultures showed the minimum values for vitamin E.