Production and characterization of Acidothermus cellulolyticus endoglucanase in Pichia pastoris

The endoglucanase (E1) from Acidothermus cellulolyticus has been used extensively in cellulase research. The goal of this work was to produce high levels of this enzyme in a system that facilitates purification. A codon-optimized synthetic gene for A. cellulolyticus E1 with a C-terminal histidine tag was cloned into the genome of Pichia pastoris. Strain KM71H expressed the most enzyme, with a yield of 550mg/L culture supernatant. The temperature optimum (80°C) and pH optimum (5.1) of the purified enzyme agree with previously determined values for the enzyme produced in other systems. Michaelis-Menten kinetic parameters were determined, using a fluorescent substrate (methylumbelliferyl-β-d-cellobioside) at various temperatures. This thermostable enzyme can be used in future cellulosic biofuels-related research.     

Distribution pattern of groundfishes hooked along a row of setline in the shallower part of the continental slope in the Bering Sea 2 bathymetric difference in relative abundance in relation to distribution pattern

1. This report demonstrates the well-defined bathymetric distribution of relative abundance of groundfishes in relation to the distribution pattern conjectured from the records of catch along a row of setline with remarkably large variation in the settled depth (from shallower than 350 m to deeper than 700 m) observed around 58⁰ 18′ N and 175⁰ 28′ W on Aug. 24, 1962.
2. The results of the analyses are depicted in Fig. 1. It is found that halibut, true cod and Sebastodes sp. (or Menuke in Japanese) show sharp or abrupt decrease in the relative abundance in accordance with depth whereas sablefish and rattail increase sharply. Arrow toothed halibut and ray do not show any clear bathymetric change in relative abundance and Pacific ocean perch shows decrease in the density in accordance with the disparity in the depth from the 500 m isobath.
3. The patterns conjectured from this example are compared with either those shown in other reports, the results of the observations on other examples or general view of our fishermen. And many proofs to the high reliability and wide universality of the conjectured pattern of the first four species are found out. But, for the last three species, the present results differ more or less from the general view of our fishermen and the observations on other examples.
4. For the distribution pattern, most of groundfishes incline to show chance distribution in the shallower part of the continental slope (350 m to 700 m deep) and only the species showing sharp decrease in density with increase in the depth are distributed contagiously on the shallower bottom (not deeper than 450 m).

     

Inference on Collapsibility in Generalized Linear Models

GREENLAND and MICKEY (1988) derived a closed-form collapsibility test and confidence interval for IxJxK contingency tables with qualitative factors, and presented a small simulation study of its performance. We show how their method can be extended to regression models linear in the natural parameter of a one-parameter exponential family, in which the parameter of interest is the difference of “crude” and “adjusted” regression coefficients. A simplification of the method yields a generalization of the test for omitted covariates given by HAUSMAN (1978) for ordinary linear regression. We present an application to a study of coffee use and myocardial infarction, and a simulation study which indicates that the simplified test performs adequately in typical epidemiologic settings.     

Cloning and nucleotide sequence analysis of the Lactobacillus delbrueckii ssp. lactis DSM7290 cysteine aminopeptidase gene pepC

Abstract A genomic library of Lactobacillus delbrueckii ssp. lactis DSM7290 in the low copy number vector pLG339, was screened for the presence of peptidase genes. Using the chromogenic substrate gly-ala-β-naphthylamide, which is not a substrate for any of the recently cloned peptidases of DSM7290, and the multiple peptidase deficient Escherichia coli strain CM89, allowed the isolation of clones, which contained the equivalent hydrolytic activity. To identify genes encoding the conserved catalytic active site of cysteine proteases, partial nucleotide sequencing with a degenerate oligonucleotide was performed on recombinant plasmids isolated from such clones. This allowed to identify two out of nine clones to carry the Lactobacillus pepC gene. A total of 2026 nucleotides were determined, and sequence analysis revealed a gene with strong homology to the recently cloned Lb. helveticus (73.2%) and Lactococcus lactis (51.03%) pepC genes, and the derived protein showed homology with the active site of a large number of cysteine proteases. The predicted open reading frame consists of 449 codons, coding for a protein of 50 909 Da. The enzyme is functional and extremely overexpressed in E. coli .     

CUG codons inCandida spp.

Codon CUG is used for serine instead of for leucine, its usual assignment, in several yeasts of the genusCandida. We propose a series of steps for the reassignment, including disappearance of leucine CUG and its anticodon CAG, formation of a new serine tRNA, with anticodon CAG, from a duplication of the gene for serine tRNA (IGA), and then production of CUG codons by mutation at sites that are mostly nonessential.     

Codon-modifications and an endoplasmic reticulum-targeting sequence additively enhance expression of an Aspergillus phytase gene in transgenic canola

Transgenic plants offer advantages for biomolecule production because plants can be grown on a large scale and the recombinant macromolecules can be easily harvested and extracted. We introduced an Aspergillus phytase gene into canola (Brassica napus) (line 9412 with low erucic acid and low glucosinolates) by Agrobacterium-mediated transformation. Phytase expression in transgenic plant was enhanced with a synthetic phytase gene according to the Brassica codon usage and an endoplasmic reticulum (ER) retention signal KDEL that confers an ER accumulation of the recombinant phytase. Secretion of the phytase to the extracellular fluid was also established by the use of the tobacco PR-S signal peptide. Phytase accumulation in mature seed accounted for 2.6% of the total soluble proteins. The enzyme can be glycosylated in the seeds of transgenic plants and retain a high stability during storage. These results suggest a commercial feasibility of producing a stable recombinant phytase in canola at a high level for animal feed supplement and for reducing phosphorus eutrophication problems.